Merck Job Trends

At We are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. Join a purpose-built, agile small molecule manufacturing site where your work will help bring important medicines to patients in the U.S. This facility is designed to move quickly and reliably, receiving technology transfers from commercialization sites and fast-following into production with a focus on quality, safety, and operational excellence. At our site, you’ll be part of a team committed to creating a safe, environmentally responsible, and compliant workplace where people can do their best...

Primary Responsibilities In the Development Sciences and Clinical Supply (DSCS) organization, we believe digital is the force multiplier that enables faster experiments, smarter decisions, more robust supply chains, and is ultimately redefining how we bring medicines to patients. Within DSCS, the DSCS Digital Technologies (DDT) team is building the next generation of data-rich, connected lab environments— where hardware, software, and AI-driven tools work together to accelerate pharmaceutical development. Our goal is simple but ambitious embed advanced digital capabilities into the DNA of how we work. We believe this future starts with a strong foundation of laboratory tools innovative robotics, process...

At We are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. Join a purpose-built, agile small molecule manufacturing site where your work will help bring important medicines to patients in the U.S. This facility is designed to move quickly and reliably, receiving technology transfers from commercialization sites and fast-following into production with a focus on quality, safety, and operational excellence. At our site, you’ll be part of a team committed to creating a safe, environmentally responsible, and compliant workplace where people can do their best...

In Primary Posting Language (Include Requirements For Education, Experience And Skills) For over 130 years, we have pioneered groundbreaking science. Today, we are driven by continuous innovation to develop breakthrough medicines, vaccines and technology. Rooted in direct experience on the farm and in the clinic, we work hand in hand with our customers every step of the way. Our singular focus is to empower those who care for animals, helping them manage their vital responsibility with confidence. Because when it comes to animal health, no one sees it like we do. Our Manufacturing and Warehouse Operations teams ensure product quality...

The Specialist, Manufacturing Automation is responsible for supporting the process automation and IT (computerized) systems that directly support vaccine manufacturing unit operations while actively supporting, participating in, and embracing an empowered team culture. In this role, the Specialist will work as an individual contributor as well as a team within a cross-functional group that includes Global Engineering Services, Technical Operations, Operations, Quality, Site Automation, and others. Position Responsibilities Provide technical expertise for design reviews, process hazard assessments, quality risk assessments, factory and site acceptance testing, Automation Installation/Operational qualification. Partner with cross-functional team to develop automated processes and complete successful qualification...

The Clinical and Regulatory Strategic Communications (CRSC) department within Global Clinical Trials Operations creates and delivers high-quality regulated content in support of our development pipeline and enables data sharing for our customers. We are a strategic partner that ensures excellence and compliance with applicable laws while incorporating health literacy principles in the development of public-facing materials. The Health Literacy Medical Writer, in collaboration with a project lead, develops, authors, and leads the review of accurate, clear, and compliant clinical, regulatory, and/or public‑facing documents in support of the company portfolio. The Health Literacy Medical Writer Acquires and applies knowledge and understanding...

Role Overview This role is part of a broader enterprise initiative to establish a Data Context Layer (DCL) — a foundational capability designed to provide consistent, reusable, and scalable context across enterprise data products. The DCL is intended to address challenges related to data fragmentation, lack of shared semantics, and inconsistent interpretation of data across systems and products . It establishes a unified layer for representing context, relationships, and meaning, enabling downstream products to operate with greater consistency, interoperability, and intelligence. In addition, the DCL plays a critical role in enabling agentic AI capabilities across the enterprise by providing the...

As a Cardiovascular Disease Specialist, you will drive meaningful patient impact by leveraging our scientific expertise and serving as the primary contact for customers within your assigned territory. As a key member of the local Customer Team, you will collaborate closely with Account Executives, Integrated Delivery Systems leaders, and other field colleagues to deliver seamless, patient-focused solutions. Territory Assignment This is a field-based sales role responsible for covering a Greensboro, Asheboro, Burlington, High Point, Mount Airy, Winston Salem, NC territory. Travel (%) depends on the needs of the territory and where the selected candidate resides, and overnight travel may be...

As part of the Cyber Fusion Center (CFC), the Operational Technology (OT) Cyber Security Analyst supports efforts to identify, analyze, and remediate cyber security risks across manufacturing and OT environments. This role works closely with internal teams and stakeholders to strengthen cybersecurity posture, improve cyber hygiene, and support operational activities across OT infrastructure. The OT Cyber Security Analyst assists with cyber security operations including vulnerability management, threat monitoring, incident response, and stakeholder coordination. The role provides an opportunity to develop technical expertise in OT security while contributing to the protection of manufacturing environments. This role works under the supervision of...

Maintenance Planner- Specialist Engineering Are you passionate about ensuring the smooth operation of maintenance activities in a dynamic and innovative environment? Join Responsibilities Assign codes to work orders. Make field inspections and determine appropriate job work scopes. Develop work plans for maintenance jobs with necessary information to allow efficient scheduling, assignment, and execution of maintenance work. Create, use, and maintain plant history and other technical files to update information in current job plans to anticipate and avoid job delays. Perform purchasing duties as required. Stage materials and special tools as required. Evaluate job feedback to improve job plans. Stay...

Translational Medicine is responsible for early clinical development of novel therapeutics, working in close collaboration with Immunology Discovery Sciences and late-stage Immunology Clinical Research. We work with all therapeutic areas within our Research Division with the role focused on Immunology. Principal Scientist (Medical Director level or known internally as Clinical Directors) must have a strong background in basic and/or clinical translational research and a desire to work collaboratively across different therapeutic areas. Translational Medicine is specifically responsible for Leadership of the early clinical development strategy for novel therapy programs from Preclinical Candidate approval through Clinical Pharmacology testing (Phase 1), and...

CANDIDATE MUST RESIDE IN ONE OF THE FOLLOWING LOCATIONS Texas, Illinois, Arizona, Florida, California, NY, Colorado The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our company's policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites. Actively develops and expands the territory for clinical research, finding and developing new...

The Associate Director, Project Management, within Metrics, Analytics & Performance (MAP) will lead project management related to the development, delivery, & maintenance of a portfolio of metrics/analytics projects to support strategic decisions, improve planning/execution, and monitor performance across our portfolio, studies & processes within Global Clinical Trial Operations (GCTO). Responsibilities include but are not limited to Collecting, assigning, tracking, and prioritizing requests from users requiring modifications (upgrades or bug fixes) to new and/or existing systems Manage timelines and resource management through development (i.e. Agile, Waterfall) and release (inc. communication & training) Approve change requests for upgrades/bug fixes/data changes and coordinate...

The Associate Director, our Research & Development division and BD&L Communications, will support the creation and implementation of communications strategies, plans and tactics that showcase our Company's Research Laboratories discovery and early pipeline efforts across our Company's core focus areas and s capabilities. This individual will also support the execution of internal and external communications related to business development and external collaborations that augment our Company's pipeline. The individual will drive communications initiatives that further our Research & Development division reputation as a leading scientific organization, and employer and partner of choice The position will report to the Director, our...

As part of the Global Clinical Supplies (GCS) organization, the Process Stewards work at the interface between core business processes and SAP capabilities, helping to enable efficient business operations, support enhancements, and drive innovation. The Senior Specialist, GCS Process Steward ensures clinical supply chain processes are clearly defined and documented, and that they are supported by the right workflows, stakeholders, SME network, and tools such as SAP. The Process Steward Team works closely with end users and process owner communities to ensure processes meet current and evolving business needs. Process Stewards also provide oversight and expertise in the SAP solution...

The Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the Metabolism section of the Atherosclerosis & Metabolism therapeutic area, with a particular focus on MASH (Metabolic Dysfunction-Associated Steatohepatitis) and other obesity-related disorders. Travel on company business about twenty (20) percent of the time to manage future or ongoing clinical research projects. Qualifications Education M.D or M.D./Ph.D. Required Must have experience in industry or as senior faculty in academia Minimum of 3 years of experience in clinical medicine Minimum of 3-5 years of industry experience in...

The Clinical and Regulatory Strategic Communications (CRSC) department within Global Clinical Trials Operations creates and delivers high-quality regulated content in support of our development pipeline and enables data sharing for our customers. We are a strategic partner that ensures excellence and compliance with applicable laws while incorporating health literacy principles in the development of public-facing materials. Acquires and applies knowledge and understanding of medical writing responsibilities, including design, planning, authoring, editing, and review of accurate, clear, high-quality documents that reflect applicable medical writing best practices (e.g., lean writing, health literacy). Demonstrates growing competence and independence in preparing clinical regulatory (e.g.,...

Animal Health — NORAM Digital Team Digital Business Liaison, Livestock Function AD, Omnichannel Digital Strategy — Livestock Reports To Director, Digital Operations Partners With Companion Animals Brand/Species marketing teams; Digital Operations team (Content, Analytics, Web, SFMC), Global Costumer engagement team, IT, among others. Location Lenexa, KS — Hybrid (3 days/week onsite) Role Purpose The Digital Business Liaison is the strategic connective layer between the Livestock business (marketing teams) and the Digital Operations execution engine. Acting as a true business partner. This person aligns business strategy across the full digital ecosystem (web, email/Sales Force Marketing Cloude (SFMC), digital content) into cohesive...

Position Description Rahway, NJ site has an opening for a Sterile Production Supervisor on 1st shift. The Formulation, Laboratory, and Experimentation (FLEx) Center is a new multi-modality (small molecule, biologics, vaccine) Drug Product development and Good Manufacturing Practice (GMP) clinical manufacturing plant in Rahway, New Jersey. The Sterile Production Supervisor manages a team of technicians for daily operations. Accountability First line operations supervisor with a team of individual contributor production direct reports Ensure that shift objectives are achieved while reliably supplying quality product at a competitive cost consistent with all applicable internal and external regulations for quality (GMP), safety, etc....

The Senior Director, Functional Area Geography Lead, GDMS Clinical Data Management (CDM Country Lead) provides strategic direction and governance to ensure consistent data-management delivery, quality, and compliance. The role oversees resource optimization, operational performance, and organizational effectiveness, driving cross-functional alignment with functional and GDMS (Global Data Management & Standards) leadership to enhance delivery, talent development, and scalability within assigned country. Strategic Leadership & Geographic Strategy Provide strategic direction within assigned country; ensure consistent execution, quality, and compliance; develop country-specific objectives aligned with organizational priorities. Serve on the functional area's leadership team as assigned; represent geographic and functional perspectives in GDMS...

The Associate Director, Enterprise Context & Data Foundations role is responsible for accelerating business value from enterprise data by establishing the semantic, contextual, and business foundations that enable analytics, AI, Copilots, and agentic products at scale. This leader serves as the bridge between business stakeholders, product teams, and technology organizations, ensuring data is organized, contextualized, and governed in a way that enables trusted decision-making and AI-powered business outcomes. The role focuses on defining business meaning, reusable context, semantic models, business rules, metadata, taxonomies, ontologies, and knowledge assets that power agentic solutions across the enterprise. Engineering teams provide the technical implementation...

CANDIDATE MUST RESIDE IN ONE OF THE FOLLOWING LOCATIONS Illinois, Colorado, South Florida, New York, California, Houston, Dallas The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites. Actively develops and expands the territory for clinical research, finding and developing...

Under the supervision of a Senior Specialist or Associate Director, the Maintenance Scheduler is responsible for building effective maintenance schedules that can be efficiently executed by the maintenance team, to minimize operational downtime and maximize mechanic productivity. The Scheduler provides strategic scheduling support for assigned area, which may include vaccine bulk manufacturing, filling, lyophilization, packaging, Quality Lab Ops and/or support utilities including power, HVAC, steam, WFI and controlled temperature units. The maintenance scheduler role is predominantly forward-looking and seldom becomes involved in work execution. The scheduler will work collaboratively with all stakeholders, drive work prioritization, and engage the proper resources...

The Senior Specialist, Sales Force Effectiveness Role supports the advancement of field effectiveness strategies for the U.S. Oncology Business Unit across customer-facing sales and key account teams. This role translates commercial objectives into actionable initiatives that enhance HCP engagement, strengthen territory productivity, and drive achievement of business goals. In close partnership with cross-functional stakeholders—including marketing, analytics, operations, and finance—the role contributes to strategic planning, delivers data-driven insights, and enables consistent execution of best practices across the field. This position also plays a key role in business planning and resource optimization, supporting sales leadership in making informed, data-driven decisions across customer...

The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Early Oncology therapeutic area. Our company's Oncology medicines span all phases of clinical development (pre-clinical to post-licensure). The Clinical Director may manage the entire cycle of clinical development for their signed studies including study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. Role Responsibilities Specifically, the Clinical Director may be responsible for Planning clinical trials (designing, collaborating on operational plans, etc.) based on the clinical development strategy Medical oversight and overall conduct of ongoing or new clinical...

The Senior Director, Functional Area Geography Lead, GDMS Clinical Data Management (CDM Country Lead) provides strategic direction and governance to ensure consistent data-management delivery, quality, and compliance. The role oversees resource optimization, operational performance, and organizational effectiveness, driving cross-functional alignment with functional and GDMS (Global Data Management & Standards) leadership to enhance delivery, talent development, and scalability within assigned country. Strategic Leadership & Geographic Strategy Provide strategic direction within assigned country; ensure consistent execution, quality, and compliance; develop country-specific objectives aligned with organizational priorities. Serve on the functional area's leadership team as assigned; represent geographic and functional perspectives in GDMS...

The Regulatory Affairs Headquarters Principal Scientist is responsible for development and implementation of global regulatory strategy for their assigned projects in the Vaccines and Infectious Disease therapeutic area. Primary activities include, but are not limited to Functions with a high degree of independence and provides regulatory oversight for assigned products, functioning as the single, accountable, global regulatory point of contact on those projects within Global Regulatory Affairs and Clinical Safety (GRACS) and external to GRACS. Develops worldwide product regulatory strategy to optimize label and obtain shortest time to approval by regulatory agencies for multiple indications simultaneously. Provides expert advice to...

Associate Principal Scientist, Process Chemistry The Process Chemistry organization, located at our Rahway, NJ site, is seeking a highly motivated and accomplished scientist with deep expertise in flow chemistry and continuous processing to join the Catalysis and Flow Lab. This position offers an opportunity to play a key role in advancing our pipeline of drug substances, including small molecules, macrocyclic peptides, and bioconjugates, by developing and implementing robust, sustainable, and efficient API manufacturing processes from discovery through commercialization. The successful candidate will lead laboratory experimentation in flow chemistry, develop and implement novel continuous processing technologies, enable new chemical transformations, and...

Animal Health — NORAM Digital Team Digital Business Liaison, Companion Animals Function AD, Omnichannel Digital Strategy — Companion Animals Reports To Director, Digital Operations Partners With Companion Animals Brand/Species marketing teams; Digital Operations team (Content, Analytics, Web, SFMC), Global Costumer engagement team, IT, among others. Location Rahway, NJ — Hybrid (3 days/week onsite) Role Purpose The Digital Business Liaison is the strategic connective layer between the Companion Animals business (marketing teams) and the Digital Operations execution engine. Acting as a true business partner. This person aligns business strategy across the full digital ecosystem (web, email/Sales Force Marketing Cloude (SFMC), digital...

The Vaccine Customer Representative (VCR) supports customers by providing clinical information on our Company’s vaccines, as well as education and resources. They do this to support customer operational and financial needs such as reimbursement information and contract adherence in an effort to help the provider or system increase their immunization rates among appropriate patients and help protect them from vaccine preventable diseases. The Vaccine Customer Representative (VCR) is the primary point of contact for a variety of customers within their assigned geography. These customers may include health care providers such as physicians, nurses, pharmacists as well as quality directors, immunization...

Position Responsibilities We are seeking a Growth and Improvement-minded Data Services Specialist in Quality Control that can help drive our Strategic Operating Priorities. Invent | Pursue the Most Promising Internal and External Science to Address Significant Unmet Medical Needs Execute | Prioritize Resources Behind Our Key Growth Drivers (Oncology, Vaccines, Select Specialty Areas, Animal Health) While Optimizing Our Base Business) Adapt | Develop Our People, Culture and Business Model to Evolve with a Dynamic Landscape Diverse Talent | We are committed to providing an inclusive and welcoming environment with supporting leadership behaviors because having a high performing, engaged workforce is...

Operational Shift Team Lead — Emergency Response, Safety & Security Leads daily emergency response, safety, and security operations across the site, including fire protection, hazardous materials coordination, loss prevention, project support, and related services. Conducts audits and surveys to identify risks and evaluate controls. Enforces site requirements for property security, access, traffic, parking, and employee conduct. This role requires shift work, including weekends and public holidays. Primary Responsibilities Operations Oversee shift operations to ensure tasks are completed efficiently and in compliance with site procedures. Conduct thorough shift turnovers to brief incoming teams on ongoing issues and special instructions. Maintain operating...

We are seeking an experienced, strategic, and inspirational sales leader to lead the Immunology field sales team. This leader will be accountable for delivering multi-billion dollar opportunity, managing operating expenses, driving market development, and ensuring compliant execution across a high-performing immunology sales organization. Reporting to the Associate Vice President, US Pharma, Sales and serving as a member of the US Pharma Sales Leadership team, the Executive Director will set strategy and operational plans, lead the field sales teams, and partner closely with Marketing, Market Access, Sales Operation, Training, and other stakeholders to deliver sustainable commercial growth and superior customer engagement....

Responsibilities Provide high quality statistical programming analysis and reporting deliverables for global stakeholders, within our Research and Development division. Gather and interpret user requirements for analysis and programming requests in close collaboration with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data, transform the data into analysis/modeling datasets, and develop tables and figures according to statistical/modeling analysis plan. Partner with stakeholders to solve problems and reduce the amount of programming tasks being completed by stakeholders to facilitate an increase in efficiency and compliance for statistical/modeling analyses. Write programs to analyze data with statistical methods which are not currently available through...

Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity, knowledge, imagination, skill and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your...

The Translational Genome Analytics group within the Data, AI & Genome Sciences Department is recruiting an Associate Director (Associate Principal Scientist) to join our data science team. We are seeking an experienced and innovative computational scientist to perform data mining of molecular data and inform decisions across all stages of our company’s expanding oncology pipeline. The successful candidate will Enable reverse translation form clinical datasets to inform biomarker discovery, combination strategies, and novel target identification linked to molecularly defined patient populations with unmet medical need. Analyze, summarize, and visualize the findings from large multi-modal clinico-genomic datasets which include bulk RNAseq,...

Bioprocess Technician Welkom in ons team In De Bilt zoeken we enthousiaste Bioprocess Technicians met oog voor detail, die willen bijdragen aan een innovatieve biotechomgeving. Op onze productielocatie maken we vaccins voor pluimvee die in meer dan 100 landen worden gebruikt. Zo verbeteren we dierenwelzijn én versterken we voedselzekerheid wereldwijd. Bij ons draait het om samenwerking en groei. Je werkt samen met collega’s van diverse achtergronden in een veilige, leerzame omgeving waarin je jezelf kunt ontwikkelen en direct bijdraagt aan een betekenisvol doel. Over de functie Als Bioprocess Technician speel je een belangrijke rol in het productieproces van onze vaccins....

Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety First, Quality Always” mindset striving for continuous improvement. We work in the local plant connected to our global manufacturing network to ensure the highest quality of raw materials, intermediates and finished products. Director – Integrated Process Team (IPT), Operations ACCOUNTABILITY Promote a Safety First, Quality Always culture that supports the mission of delivering uninterrupted, unconstrained, compliant, reliable supply through behaviors and principles that drive continuous improvement. Ensure that short term and long-term Integrated Process Team (IPT) objectives are achieved...

Department - Global Regulatory Affairs and Clinical Safety - Vaccine & Infectious Disease Brief Description of Position- The Regulatory Affairs Headquarters Principal Scientist is responsible for development and implementation of global regulatory strategy for their assigned projects in the Vaccines and Infectious Disease therapeutic area. Primary activities include, but are not limited to Functions with a high degree of independence and provides regulatory oversight for assigned products, functioning as the single, accountable, global regulatory point of contact on those projects within Global Regulatory Affairs and Clinical Safety (GRACS) and external to GRACS. Develops worldwide product regulatory strategy to optimize label...

The Sr. Specialist, Marketing Procurement is responsible for supporting strategic sourcing, supplier management, contract management, and stakeholder engagement activities across Marketing Services categories within our Animal Health division. Key categories include, but are not limited to, Advertising, Media (Traditional and Digital), Market Research, Public Relations, Branding, Creative and Design Services, Communications, Print, and Events. This position is based in Rahway, New Jersey, and reports to the Global Indirect Procurement Director within the Global Supplier Management (GSM) organization. The role serves as a strategic business partner to Marketing, Sales, Communications, Finance, and other cross-functional stakeholders, supporting the delivery of procurement strategies...

Senior Scientist, Analytical R&D At Summary, Focus and Purpose The Viral Vaccine Senior Scientist will provide subject matter expertise to support to the Viral Vaccine franchises (and other products, as required) to drive reliable and compliant supply of inline products with a line of sight for pipeline assets into QC. Responsibilities Serve as a Subject Matter Expert supporting molecular biology and live virus vaccine potency methods. Engage in inline and pipeline method optimization, testing, and troubleshooting of molecular biology-based and cell-based methods (vaccine and biologic). Collaborate with a large team of colleagues to deliver high-quality results for multiple products....

The mission of the Analytics & Technology Systems QA group is to provide the foundation to identify, explore, and efficiently develop solutions to enhance our quality oversight activities. Under the direction of the Senior Director, Analytics & Technology Systems of our Research & Development Division QA, we are seeking an Associate Director, Data Science & AI Solutions , to join our R&D Quality Assurance Analytics & Tech Systems team. In this role, you will bridge the gap between hands-on advanced software development and strategic business partnership. You will lead the design, deployment, and long-term lifecycle of our next-generation AI and...

Shape the Future of Vaccines We are seeking an exceptional leader to serve as Executive Director, Vaccine Drug Product Development , a highly visible role responsible for providing strategic, scientific, and organizational leadership across our vaccine portfolio. This individual will define and drive drug product strategy from early development through commercialization, helping bring innovative vaccines to patients worldwide. As a key leader, you will influence portfolio direction, guide critical investment and launch-readiness decisions, and build the organizational capabilities needed to meet both current and future business priorities. This is a unique opportunity to lead at the intersection of science, strategy,...

Our Company’s purpose is to use the power of leading-edge science to save and improve lives around the world in the areas of prescription medicines, vaccines, biologic therapies, and animal health products and technology solutions. We are committed to patients. Our Account Management roles are critical in helping to drive the success of our mission and to ensure profitable access to our products. The Associate Director, Urology - Oncology Key Accounts is the main point of contact for Our Company with large community urology group practices. They play a crucial role in establishing Our Company as an industry leader, supporting...

Manager, First Shift Quality Control At Join our team and contribute to our mission of making a difference in global health. What You'll Be Doing You'll provide guidance and supervision to hourly Microbiology technicians, ensuring all testing and support activities are completed efficiently. Motivate, train, and resolve problems for your team while maintaining a compliant and safe environment. Administer personnel policies in accordance with the local bargaining agreement. Manage critical testing and/or assaying of validation, raw material, process intermediates, and finished product samples. Supervise hourly employees in their testing duties, including scheduling work assignments based on priorities. Promote teamwork...

Role Summary The Associate II, Administrative Assistant provides proactive, high-quality, flexible, and reliable administrative support to SCIS team members at Band 500 and below. This role assists with administrative functions relating to organization and communication across the team and ensures the efficient operation of the department and its team members. In addition to supporting the daily functions of the team, the role supports various department-related committees and meetings that enhance the department and further its goals. Responsibilities and Primary Activities Manages calendars, prepares correspondence and reports, and reliably handles confidential and politically sensitive issues. Often serves as an initial point...

For over 130 years, we have pioneered groundbreaking science. Today, we are driven by continuous innovation to develop breakthrough medicines, vaccines and technology. Rooted in direct experience on the farm and in the clinic, we work hand in hand with our customers every step of the way. Our singular focus is to empower those who care for animals, helping them manage their vital responsibility with confidence. Because when it comes to animal health, no one sees it like we do. Summary of the job Our Sr. Territory Managers interact face to face with our customers, understand their needs and consult...

This role is primarily accountable for the end-to-end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, our Company policies and procedures, quality standards and adverse event reporting requirements internally and externally. The CRM could be responsible for a particular study for several countries in a cluster. Responsibilities include, but are not limited to Main Point of Contact (POC) for assigned protocols and link between Country Operations and clinical trial team (CTT). Responsible for project management of the assigned studies pro-actively plans, drives and tracks execution and performance of deliverables/timelines/results to meet...

Senior Specialist, New Product Introductions Our ability to excel depends on the integrity, knowledge, imagination, skill, and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. Direct Materials Procurement- New Product Introduction is responsible for the development and implementation of all supplier management strategies and initiatives, improving supply chain resiliency, and driving improvements in cost, supplier performance and working capital, in support...

Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety First, Quality Always” mindset striving for continuous improvement. We work in the local plant connected to our global manufacturing network to ensure the highest quality of raw materials, intermediates, and finished products. The Quality Control Manager provides quality oversight of the qualified utilities and facility environmental monitoring sampling at the West Point vaccine manufacturing site. The Manager, with guidance from the Associate Director of Environmental Monitoring, ensures the qualified utilities (Water-for-Injection, Clean Steam, Compressed Gases) and Facility EM (Surface, Air,...

The HIV Customer Representative is a key member of the Customer Team and plays a critical role in supporting our Company's customer centric business model. This position is responsible for working with the Customer Team to understand and identify customer needs, supporting pull-through activities relative to the customer strategy, keeping with our Company's values and standards as governed by our policies and ensuring that our Company is viewed as demonstrating better health outcomes to healthcare professionals and their patients. The HIV Customer Representative demonstrates professionalism and leadership by modeling the required knowledge for successful execution of all Field Sales competencies....

Associate Principal Scientist Our company's Pharmaceutical Sciences & Clinical Supplies organization translates molecules to medicines, working from the discovery interface through registration stability manufacturing by designing, developing and scaling-up the formulation, device, and manufacturing process. Driving drug product design from the bench top to the Good Manufacturing Practice (GMP) manufacturing facilities, our Scientists use cutting edge science to transform drug delivery and manufacturing technology to positively impact patients. The successful candidate will be a passionate scientist with strong academic fundamentals and a drive to develop new medicines to improve human health. In this role, the individual will be responsible...

We aspire to be the premier research-intensive biopharmaceutical company. At the forefront of research, we deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. Join our team and be part of a company that uses the power of leading-edge science to save and improve lives around the world. The Associate Director, Engineering within Biologics External Manufacturing Technology is accountable for achieving excellence in Compliance, Supply, Continuous Improvement & Cost Reduction in partnership with our internal technical partners and External Partner (EP) leadership, supporting the Vaccines and Biologics businesses. This individual works in collaboration...

Team Overview The GRACS RDDH team assists in bringing new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance across regulatory agencies. We are an international network on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices, and solutions to the world through a highly regulated industry. Position Overview Under the direction and guidance of the Executive Director, Regulatory Digital Health the incumbent will assist in driving the overarching strategy for the Digital Health Medical Device Modality in partnership with the Global Regulatory Leads (GRLs), Chemistry, Manufacturing and...

We aspire to be the premier research-intensive biopharmaceutical company with over 130-year history. We’re at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. Our success is driven by putting patients first, operating with the highest integrity, and committing fully to our vision to make a difference in the lives of people globally. With our varied pipeline of oncology, immunology, vaccines, biologics, small molecules, and newer modalities, we are at the forefront of research to advance the prevention and treatment of diseases such as cancer, cardiometabolic diseases, eye...

The Finance Director of Global Oncology will be a role responsible for supporting financial planning and analysis, an immunotherapy medication, a treatment, and other in line assets as well as the coordination of the overall Oncology consolidation for planning purposes. Will work extensively with the Marketing Operations and GDL’s as a key business partner. This role will provide insights and analytics to support business decisions while we continue to grow the oncology portfolio across all regions. This role will report to the Global Oncology Associate Vice President. Key Responsibilities Provide Financial Support to Marketing operations and coordinate the LCM team...

Senior Scientist, Predictive Immune Biomarkers (R3) The Precision Genetics group within the Data, AI and Genome Sciences Department is seeking a Senior Scientist to join our Computational Precision Immunology team in Cambridge, MA. We are looking for a skilled data scientist with extensive experience to develop predictive biomarkers in immunology based on multi-modal and multi-scale data analyses. Key Responsibilities Foundation Models Build, fine-tune, troubleshoot, and benchmark foundation models for predictive immune biomarker discovery. Multi-omics Analysis Perform quality control (QC) and analysis of different molecular data types including bulk and single-cell RNA-seq (e.g., Limma, Seurat, scanpy), spatial transcriptomics (e.g., CosMx, 10x...

Our Company is seeking exceptional chemists for positions within the Discovery Chemistry Department. The successful candidate will join multidisciplinary, highly collaborative discovery teams to invent novel medicines by applying innovative synthetic chemistry, analytical techniques, and data analysis to design and synthesize drug candidates and intermediates. In addition, you’ll have the opportunity to expand your knowledge and skills through collaborations with talented and dedicated colleagues while advancing your career. Specific responsibilities will include the following Act as an expert in the laboratory, executing on program and chemistry strategy. Develop and utilize innovative synthetic, medicinal chemistry and/or chemical biology problem solving skills...

Our Company’s purpose is to use the power of leading-edge science to save and improve lives around the world in the areas of prescription medicines, vaccines, biologic therapies, and animal health products and technology solutions. We are committed to patients. Our Account Management roles are critical in helping to drive the success of our mission and to ensure profitable access to our products. The Associate Director, Urology - Oncology Key Accounts is the main point of contact for Our Company with large community urology group practices. They play a crucial role in establishing Our Company as an industry leader, supporting...

Our Company is currently seeking an exceptional chemist to join the Discovery Process Chemistry group located at our Boston, MA site. This role offers the opportunity to join a vibrant group of innovative laboratory scientists with broad impacts across our late discovery and early development portfolios. Core responsibilities include the development of innovative solutions to complex chemistry problems across a portfolio of projects in the discovery phase, from lead identification through candidate selection. A successful candidate is expected to apply cutting edge methodologies to synthetic route design in order to enable medicinal chemistry research and accelerate the delivery of target...

The Principal Trial Manager is responsible for leading projects and initiatives to improve the quality and compliance of the data management functional areas in addition to the regular responsibilities as an individual Trial Manager. The Principal Trial Manager is responsible and accountable for the successful execution of the clinical data management strategy for one or more drug or vaccine trials within the TM role. Will be responsible for leading and/or representing data management functional areas or GDMS in cross-functional initiatives and project teams as deemed appropriate. Principle Trial Managers will possess end-to-end data management knowledge with strong project management and...

As a Cardiovascular Disease Specialist, you will drive meaningful patient impact by leveraging our scientific expertise and serving as the primary contact for customers within your assigned territory. As a key member of the local Customer Team, you will collaborate closely with Account Executives, Integrated Delivery Systems leaders, and other field colleagues to deliver seamless, patient-focused solutions. Territory Assignment This is a field-based sales role responsible for Albany, GA covering Albany , Valdosta, Tifton and Waycross, GA. Travel percentage depends on the needs of the territory and where the selected candidate resides, and overnight travel may be required about 25...

Job Summary The Senior Specialist, GEO Content supports our Company's GEO & AI Discoverability program within the Web Experience & Discovery Product Team by advising global brand and marketing teams on how to structure, optimize, and govern approved content so that it is more findable, understandable, and citable by generative AI and answer engine platforms. This role connects content decisions to AI visibility and citation outcomes. The successful candidate will partner closely with analysts within the broader Digital Channels & Orchestration team to review AI discoverability performance across global HCP and consumer websites, conduct GEO (Generative Engine Optimization) content audits,...

Principal Scientist Our company's Pharmaceutical Sciences and Clinical Supply (PSCS) organization translates molecules to medicines, working from the discovery interface through registration stability manufacturing by designing, developing and scaling-up the formulation, device, and manufacturing process. Driving drug product design from the bench top to the Good Manufacturing Practice (GMP) manufacturing facilities, our Scientists use cutting edge science to transform drug delivery and manufacturing technology to positively impact patients. The successful candidate will be a passionate scientist with strong academic fundamentals and a drive to develop new medicines to improve human health. In this role, the individual will be responsible...

Our company is dedicated to delivering innovations that extend and improve the lives of patients worldwide. Our team of forward-thinking individuals achieve this through an unwavering commitment to supporting accessibility to medicine, providing new therapeutic options, and collaborating with payers and government to ensure that people who need medicines have access to them. At our company, our focus is on innovation and launch execution excellence; we translate breakthrough science into innovative medicines that help people around the globe. The Associate Director, US HIV Payer Marketing, is responsible for developing market access strategies and solutions for the assigned brands. The individual...

With support of other Clinical Research Manager's (CRMs) and/or Therapeutic Area Head (TAH) / Clinical Research Director (CRD), this role is accountable for the end-to-end performance and project management for assigned protocols in a country in compliance with International Council for Harmonisation Good Clinical Practice (ICH-GCP) and country regulations, our company's policies and procedures, quality standards and adverse event reporting requirements internally and externally. The Associate Clinical Research Manager (aCRM) could be responsible for a particular study for a country or a cluster. Responsibilities include, but are not limited to Main Point of Contact (POC) for assigned protocols and link...

The U.S. PAH Consumer Marketing team is seeking an Associate Director to lead the consumer patient adherence strategy for our PAH drug. This is a high-impact opportunity to shape and scale a patient-centered program designed to help appropriate patients start therapy with confidence, stay engaged over time, and navigate key moments in their treatment journey. This leader will own the strategy, execution, and optimization of the adherence program, partnering across Marketing, Patient Services, Market Access, Digital, Data & Analytics, Medical, Legal/Compliance, agencies, and other key stakeholders. The role requires a strong strategic leader who can translate patient insights, business priorities,...

Our Regulatory Affairs team in General Medicine advances medical innovation to patients by establishing clear, timely, and robust strategies for registration enabled by engagement with global health authorities. We work across functions and geographies to advance development programs and maintain licensure for the General Medicine portfolio worldwide. We seek a leader with a growth mindset, demonstrated by intellectual curiosity and the ability to navigate complex regulatory challenges with rigor and professionalism. The Senior Principal Scientist, Regulatory Affairs Liaison is responsible for the development and implementation of worldwide regulatory strategy for programs in the General Medicine therapeutic area with specific focus...

Global Market Access (GMAx) has a single purpose To save and improve lives by delivering optimal access for our medicines and vaccines across the globe at a price reflective of their value. Within GMAx, the Global Pricing Operations (GPO) team operates as a strategic, consulting-style partner to the broader organization. This role leads the Pharma Practice Area and serves as GPO’s primary strategic partner for Pharma pricing operations, analytics, and capability needs across launch, inline, and lifecycle management priorities. The Director, Pharma Pricing Operations & Analytics is a senior thought leader responsible for driving value realization from our best-in-class data...

The Biologics Process Research & Development organization within our Company Research Labs is responsible for developing the drug substance manufacturing processes for our Company's biologics pipeline. We work closely with colleagues in Discovery, Pre-clinical, and Early Development to rapidly develop processes for various biotherapeutics and efficiently produce material to supply clinical trials. We are also responsible for commercial process development, and development and implementation of new technologies. We work with our partners in our Company Manufacturing Division to commercialize and launch new products. This role will support the Next Generation Biologics (NGB) facility, which will be a premier, state-of-the-art facility,...

For over 130 years, we have pioneered groundbreaking science. Today, we are driven by continuous innovation to develop breakthrough medicines, vaccines and technology. Rooted in direct experience on the farm and in the clinic, we work hand in hand with our customers every step of the way. Our singular focus is to empower those who care for animals, helping them manage their vital responsibility with confidence. Because when it comes to animal health, no one sees it like we do. Do you see inefficient processes as opportunities? Are you energized by solving complex problems and building practical solutions that make...

The Senior Director, Clinical Science – Lung is responsible for providing strategic Clinical Science leadership across the lung disease area, with accountability spanning multiple studies, programs, and assets. Reporting to the Executive Director – Lung, Head and Neck, and Gastrointestinal, or to the Head of Clinical Science Oncology, this role contributes to disease area strategy by applying deep therapeutic expertise to guide Clinical Science approaches, support development planning, and promote consistency in scientific standards, medical data review practices, and decision-making across the portfolio. The individual in this role is expected to bring deep knowledge of lung cancer, including disease biology,...

The HIV Customer Representative is a key member of the Customer Team and plays a critical role in supporting our Company's customer centric business model. This position is responsible for working with the Customer Team to understand and identify customer needs, supporting pull-through activities relative to the customer strategy, keeping with our Company's values and standards as governed by our policies and ensuring that our Company is viewed as demonstrating better health outcomes to healthcare professionals and their patients. The HIV Customer Representative demonstrates professionalism and leadership by modeling the required knowledge for successful execution of all Field Sales competencies....

Principal Scientist, Biologics, Sterile Drug Product Commercialization As part of Our Company’s Manufacturing Division, the Sterile Drug Product Commercialization group provides the technical process leadership and laboratory capabilities for late stage and commercial drug product processes for biologics. It is the division’s leader in sterile product and process development, responsible for late-stage commercialization activities including process scale up, technology transfer to internal and external sites, process validation, authoring of regulatory submissions and support of significant manufacturing investigations. The group is responsible for establishing the science, engineering and knowledge required for today’s innovative and accelerated commercialization of biologics and combination products....

For over 130 years, we have pioneered groundbreaking science. Today, we are driven by continuous innovation to develop breakthrough medicines, vaccines and technology. Rooted in direct experience on the farm and in the clinic, we work hand in hand with our customers every step of the way. Our singular focus is to empower those who care for animals, helping them manage their vital responsibility with confidence. Because when it comes to animal health, no one sees it like we do. Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety...

Our Quality Assurance group ensures our products are manufactured, processed, tested, packaged, stored and distributed in alignment with our incredibly high standards of quality and meet all regulatory requirements. Partnering across our internal manufacturing facilities, external contract manufacturers and suppliers we create an interdependent global manufacturing network committed to deliver a compliant, reliable supply to customers and patients on time, every time, across the globe. The Quality Line Oversight Program at West Point is an entry level 2 year program with 8 month rotations focused on providing hands-on experience in pharmaceutical quality assurance supporting our Company’s largest and most complex...

The Global Commercial Metabolism Team is responsible for shaping the global commercial strategy for our Obesity portfolio, with a focus on building differentiated, insight-driven strategies that position assets for long-term success in a highly dynamic and competitive market. The Associate Director, Global Marketing – Obesity will operate at the intersection of strategy, asset development, and customer insight, with responsibility for advancing overall global commercial strategy across obesity assets in development. This individual will bring a dual focus on healthcare professional (HCP) and healthcare customer (HCC) audiences, helping define how each asset can be positioned, differentiated, and valued in the future...

At We are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. Join a purpose-built, agile small molecule manufacturing site where your work will help bring important medicines to patients in the U.S. This facility is designed to move quickly and reliably, receiving technology transfers from commercialization sites and fast-following into production with a focus on quality, safety, and operational excellence. At our site, you’ll be part of a team committed to creating a safe, environmentally responsible, and compliant workplace where people can do their best...

Senior member of Identity & Access Management working as part of a global team to support a fast-paced environment. Ensure conformance to established system architecture, security, regulations, standards and practices, and participate\drive their creation and upkeep. In addition to technical expertise must be proficient in managing projects through to completion, innovative, security focused, self-motivated and driven. The candidate will be a member of the global Tier 2 Identity and Access management Operations team which includes operational responsibilities across all supported platforms in organization. Good communication skills, documentation abilities and compliance experience required. Comfortable working in a team environment and able...

Our Company is a global biopharmaceutical leader with a portfolio of prescription medicines, oncology, vaccines, and animal health products. We are driven by our purpose to develop and deliver innovative products that save and improve lives. With employees operating in more than 140 countries, we offer state of the art laboratories, plants and offices that are designed to Inspire our employees as we learn, develop, and grow in our careers. We are proud of our 125 years of service to humanity and continue to be one of the world’s biggest investors in Research & Development. This position is within the...

Brief Description of Position Transact Globally to Provide Business Support to our company's Research Laboratories; Work with our company's Research Laboratories, internal partners, and global external collaborators to draft, negotiate and execute a variety of agreement types to further the knowledge, pipeline and reputation of our company. Advance discovery research via engagement and collaboration with universities, government, not-for-profits, biotech and pharma to support our company's Research Laboratories key objectives and programs, provide access to critical assets, reagents, technologies, access external innovation, and protect our company's intellectual property. Effectively work cross-functionally and collaboratively with Discovery Transaction colleagues, Corporate Legal, Patent Legal,...

At We are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. Join a purpose-built, agile small molecule manufacturing site where your work will help bring important medicines to patients in the U.S. This facility is designed to move quickly and reliably, receiving technology transfers from commercialization sites and fast-following into production with a focus on quality, safety, and operational excellence. At our site, you’ll be part of a team committed to creating a safe, environmentally responsible, and compliant workplace where people can do their best...

We are seeking an exceptional scientific leader with deep expertise in immunology, translational science, and biomarker research to join our Discovery Immunology Team. This individual will help advance our mission to discover and develop best-in-class medicines for patients with immune-driven diseases. The Senior Director, Translational and Biomarker Lead will shape and oversee translational and biomarker strategy for immunology programs, integrating discovery insights, human biology, and early clinical development. The role will guide hypothesis-driven mechanistic, preclinical, in vivo, and biomarker studies, translating complex data into clear recommendations that inform decisions across the portfolio. As a leader of multiple teams, this individual...

The Head of External Manufacturing Quality – Large Molecule leads our Manufacturing Division's global External Manufacturing Quality organization for biologics and vaccines. This leader directs a multinational team of approximately 100 professionals and establishes the quality strategy, governance, and oversight model for products manufactured, tested, packaged, released, stored, and distributed through our company's external manufacturing network. The role ensures compliance with our company's requirements, applicable regulatory expectations, and global GMP standards while enabling reliable supply, supporting timely product launches, and strengthening the execution of technology transfers across approximately 30 external manufacturing sites spanning cell banking, drug substance, and drug product...

At We are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. Join a purpose-built, agile small molecule manufacturing site where your work will help bring important medicines to patients in the U.S. This facility is designed to move quickly and reliably, receiving technology transfers from commercialization sites and fast-following into production with a focus on quality, safety, and operational excellence. At our site, you’ll be part of a team committed to creating a safe, environmentally responsible, and compliant workplace where people can do their best...

Our company a global healthcare leader, is currently seeking an Entry-Level Veterinary Associate to join our collaborative, dynamic, and inclusive Laboratory Animal Science Team at the West Point location. The successful candidate will be integral in executing research study tasks, as well as some routine veterinary and animal colony management tasks. On-site and hands-on study-related lab work will be a crucial part of the role. The role also requires rotational weekend work and the ability to apply sound technical skills to assigned tasks, often with minimal supervision. Our company values collaboration, coordination, and communication. We aim to foster an atmosphere...

The Clinical Services Operations Coordinator, under the guidance of a West Point laboratory animal resources husbandry operations, works to provide world class animal care to impact drug development and discovery and improve human health. With minimal direction and in compliance with departmental Standard Operating Procedures, our Research & Development division study requirements, as well as applicable regulations and guidelines to include USDA regs, NIH Guide and, Good Laboratory Practices, this position oversees the details of animal care and related activities of Laboratory Animal Resources, to include indirect guidance of animal care workers. Has responsibility to assist with the training, development,...

Associate Principal Scientist, Biologics, Sterile Drug Product Commercialization As part of Our Company’s Manufacturing Division, the Sterile Drug Product Commercialization group provides the technical process leadership and laboratory capabilities for late stage and commercial drug product processes for biologics and combination products. It is the division’s leader in sterile product and process development, responsible for late-stage commercialization activities including process scale up, technology transfer to internal and external sites, process validation, authoring of regulatory submissions and support of significant manufacturing investigations. The group is responsible for establishing the science, engineering and knowledge required for today’s innovative and accelerated commercialization of...

Do you enjoy understanding how business systems, data, and users work together? We are looking for a Senior Specialist, Business Systems Excellence to help shape the future of our enterprise systems ecosystem. This role will play a key part in our SAP S/4HANA transformation while helping strengthen the connected systems, data, reporting, and analytics capabilities that support business operations globally. You will work across SAP, Ariba, Aera, Databricks, and other connected platforms to ensure information flows effectively, systems remain aligned, and data can be trusted to drive decisions. This role is ideal for someone who enjoys understanding complex system landscapes,...

The Clinical and Regulatory Strategic Communications (CRSC) department within Global Clinical Trial Operations (GCTO) creates and delivers high-quality regulated content in support of our development pipeline and enables data sharing for our customers. We are a strategic partner that ensures excellence and compliance with applicable laws while incorporating health literacy principles in the development of public-facing materials. The Associate Director of Disclosure Quality and Operations overseas and leads the preparation, quality control, tracking, and submission of clinical and regulatory documents and transparency deliverables, while coordinating with stakeholders to ensure compliance, accuracy, and timely completion of regulated content. Key responsibilities may...

Sr. Specialist –Discovery Process Chemistry (P3) The Discovery Process Chemistry group within the Small Molecule Process Research & Development Department in Rahway, New Jersey is seeking a Senior Specialist to play a key role in advancing a various portfolio of discovery-stage programs, from lead identification through candidate selection. This lab-based position offers the opportunity to make a significant impact on our discovery pipeline by executing the synthesis of key starting materials and advanced intermediates that enable the rapid delivery of target compounds across early-stage programs. The successful candidate will also support kilo-lab scale syntheses and serve as a point of...

For over 130 years, we have pioneered groundbreaking science. Today, we are driven by continuous innovation to develop breakthrough medicines, vaccines and technology. Rooted in direct experience on the farm and in the clinic, we work hand in hand with our customers every step of the way. Our singular focus is to empower those who care for animals, helping them manage their vital responsibility with confidence. Because when it comes to animal health, no one sees it like we do. Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety...

Our company a global healthcare leader, is currently seeking an Entry-Level Veterinary Associate to join our collaborative, dynamic, and inclusive Laboratory Animal Science Team at the West Point location. The successful candidate will be integral in executing research study tasks, as well as some routine veterinary and animal colony management tasks. On-site and hands-on study-related lab work will be a crucial part of the role. The role also requires rotational weekend work and the ability to apply sound technical skills to assigned tasks, often with minimal supervision. Our company values collaboration, coordination, and communication. We aim to foster an atmosphere...

At Join our manufacturing division and be part of a team that is dedicated to maintaining reliable, compliant, and secure automation solutions while driving continuous improvement and digital manufacturing initiatives. Working within the Site DMO team, the Senior Specialist, Manufacturing Automation serves as the site technical lead for manufacturing automation systems supporting production operations. The role provides automation expertise across PLC, HMI, machine vision, serialization, MES, IT and OEM manufacturing systems. The position is responsible for maintaining reliable, compliant and secure automation solutions while driving continuous improvement, equipment reliability, and digital manufacturing initiatives. Emphasis is placed on packaging automation,...

Senior Scientist, Statistical Programming – Rahway, NJ Provide support to statistical programming activities for late-stage drug/vaccine clinical development projects. Be accountable for the development and execution of statistical analysis and reporting deliverables (e.g. safety and efficacy analysis datasets, tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support. Design and maintain statistical datasets that support multiple stakeholder groups which include clinical development, outcomes research and safety evaluation. Act as a key collaborator with statistics and other project stakeholders in ensuring that project plans are executed efficiently with timely and...

For over 130 years, we have pioneered groundbreaking science. Today, we are driven by continuous innovation to develop breakthrough medicines, vaccines and technology. Rooted in direct experience on the farm and in the clinic, we work hand in hand with our customers every step of the way. Our singular focus is to empower those who care for animals, helping them manage their vital responsibility with confidence. Because when it comes to animal health, no one sees it like we do. Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety...

Role Summary The Associate Director, Community Engagement Team Lead position resides in the Value & Implementation (V&I) organization, which includes Global Medical and Scientific Affairs as well as Outcomes Research. This role is responsible for leading and enabling a team of Community Engagement Specialists (CES) to execute community engagement across priority advocacy ecosystems, including patient advocacy organizations (PAOs), community-based organizations (CBOs/NGOs), and allied healthcare networks. The Associate Director / Manager serves as a critical link between field execution and organizational strategy, ensuring consistent, compliant, and high-quality engagement aligned to enterprise priorities and community needs. The role focuses on translating strategy...

Within DAGS, our AI/ML team drives innovation across disease areas by building biologically grounded and interpretable imaging pipelines. In Immunology, digital pathology plays a critical role in understanding tissue level immune mechanisms and supporting companion diagnostics. We are seeking a Senior Data Scientist with strong expertise in computer vision and biomedical imaging to develop scalable imaging foundation models and interpretable pipelines for immunology and oncology biomarker discovery. What You’ll Do Develop and train imaging foundation models for histopathology, with a focus on immune‑relevant tissue and cellular patterns. Build segmentation driven and cell‑centric pipelines (e.g., immune cell typing, spatial organization, microenvironment...

Description – Sr. Specialist, Engineering The Sterile/Liquids Pilot Plants (SLP,) located in Bldg. 17 at West Point, is part of the Pharmaceutical Sciences organization. The SLP supports the formulation and filling of clinical, stability, and developmental supplies for vaccines, small molecules, and therapeutic proteins. The SLP interfaces with a large network including multiple of our Company's Research Laboratories teams, Sterile/Liquids Commercialization (SLC), commercial supply, and other pilot plants within the PharmSci network. SLP supplies support critical program needs related to new products undergoing process development, new products undergoing scale-up, launch, and transfer to the supply network, and existing commercial products...

The Science and Regulatory Policy team is responsible for developing our company’s science and regulatory policy positions and advocating those towards industry thought leaders and regulators. The Executive Director, Enterprise Regulatory Policy Strategy provides strategic direction for our company's enterprise level regulatory policy approach across regions and markets. The Executive Director (ED) will be a strong subject matter expert in regulatory processes, policies, laws, and regulations, with a deep understanding of how regulatory policy is shaped and influenced, and the credibility, relationships, and strategic judgment required to drive alignment and advance regulatory policy priorities in direct support of our Research...

At We are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. Join a purpose-built, agile small molecule manufacturing site where your work will help bring important medicines to patients in the U.S. This facility is designed to move quickly and reliably, receiving technology transfers from commercialization sites and fast-following into production with a focus on quality, safety, and operational excellence. At our site, you’ll be part of a team committed to creating a safe, environmentally responsible, and compliant workplace where people can do their best...

Our company, a global healthcare leader, is currently seeking an entry-level Veterinary Associate to join our collaborative, dynamic, and inclusive Laboratory Animal Science Team at the West Point location. The successful candidate will execute study support and veterinary care for large and small animals supporting various research programs. This position requires weekend coverage with a Saturday through Wednesday schedule or a Wednesday through Sunday schedule. On-site and hands-on study-related lab work will be a crucial part of the role. The role also requires the ability to apply sound technical skills and animal health knowledge to assigned tasks, often with minimal...

The Senior Director, Clinical Science – Hematology is responsible for providing strategic Clinical Science leadership across the hematology disease area, with accountability spanning multiple studies, programs, and assets. Reporting to the Executive Director – Hematology, Oncology Assets and Early Development, or to the Head of Clinical Science Oncology, this role contributes to disease area strategy by applying deep therapeutic expertise to guide Clinical Science approaches, support development planning, and promote consistency in scientific standards, medical data review practices, and decision-making across the portfolio. The individual in this role is expected to bring deep knowledge of hematologic cancers, including disease biology,...

The Customer Contract Management (CCM) Contract Analyst (Senior Specialist) is responsible for contract adjudication, analysis, and customer interaction in support of our Company's managed care agreements. This position will support the Medicaid segment. The ideal candidate will possess strong leadership, technical, business, and financial acumen, and will maintain the highest level of compliance with contract terms and conditions, regulatory requirements, and applicable laws and regulations. The ideal candidate will support internal stakeholders and provide strong partnership with our Company's external managed care customers in the administration, performance reporting, and analysis of all Medicaid agreements entered into by our Company that...

As part of the Global Clinical Supplies (GCS) Organization, the Sr. Specialist, Master Data Quality Management is responsible for driving data quality, governance, stewardship, and operational excellence across critical master data domains supporting Global Clinical Supply Operations (GCSO). This role helps ensure that master data is accurate, complete, compliant, and fit-for-purpose to support planning, manufacturing, packaging, distribution, regulatory compliance, and business decision-making. The individual partners with Data Owners, Process Stewards, IT, Business Operations, and Analytics teams to establish data quality controls, monitor performance through dashboards and Key Performance Indicators (KPIs), facilitate remediation, and support continuous improvement initiatives. The role is...

The Associate Vice President (AVP), Global Commercial Leader Inflammatory Bowel Disease (IBD), Immunology will lead the global strategy and enterprise launch readiness of our company's next immunology drug for Ulcerative Colitis (UC) and Crohn’s Disease (CD) indications . The global brand leader is responsible for setting a bold aspirational commercial vision and guiding a cross-functional team to realize this vision. This is a business-critical role for our company. Our ability to make a meaningful impact on immunology diseases will be influenced by the leadership and vision of this role. The Global Commercial Leader for IBD will provide commercial input into...

Join Us in Shaping the Future of Animal Health For over 130 years, we have pioneered groundbreaking science. Today, we are driven by continuous innovation to develop breakthrough medicines, vaccines and technology. Rooted in direct experience on the farm and in the clinic, we work hand in hand with our customers every step of the way. As a Methods Specialist, you will be part of a world-class team, contributing directly to the production and testing of veterinary products that improve animal health and welfare globally. You will collaborate closely with Quality Control, Manufacturing Operations, Bioprocess Technology Solutions, Regulatory Affairs, Statistics,...

The Formulation, Laboratory, and Experimentation (FLEx) Center is a new multi-modality (small molecule, biologics, vaccine) Drug Product development and Good Manufacturing Practice (GMP) clinical supply manufacturing facility in Rahway, New Jersey. The Sterile Process Engineer role at the Senior Specialist level will leverage the individual’s leadership, technical, and communication skillsets to drive the success of our clinical manufacturing facility and organization. This role will directly support the pipeline’s most technically complex formulations and process development through process tech transfers, scale-up activities, quality investigations, change management, and authoring GMP standard operating procedures and protocols in support of sterile clinical drug product...

This Associate Director role in the External Reporting group will be focused on the emerging area of Sustainability reporting, as the Company prepares its initial regulatory sustainability filings. This position will report to the Executive Director – External Reporting and will work extensively with the Sustainability Controller to help ensure our Company is positioned for and responsive to growing global regulatory external reporting requirements related to environmental, social and governance topics. The responsibilities of this role require extensive cross functional engagement and collaboration with the Social Impact & Sustainability, Finance, Legal, IT, and Internal/External Audit teams. Specific responsibilities include supporting...

Our company a global healthcare leader, is currently seeking an entry-level Veterinary Associate to join our collaborative, dynamic, and inclusive Laboratory Animal Science Team at the West Point location. The successful candidate will execute study support and veterinary care for large and small animals supporting various research programs. This position requires weekend coverage with a Saturday through Wednesday schedule or a Wednesday through Sunday schedule. On-site and hands-on study-related lab work will be a crucial part of the role. The role also requires the ability to apply sound technical skills and animal health knowledge to assigned tasks, often with minimal...

Our Company is preparing for the potential U.S. launch of an oncology mRNA-based individualized neoantigen therapy for early stage melanoma which involves operational complexities for treatment sites and requires close coordination with cross-functional partners. To ensure site readiness and support consistent site execution, we are building a dedicated team of field-based operational roles to help educate treatment sites on the practical, logistical, and operational requirements necessary to onboard the product effectively, inform treatment sites about helpful workflows and tools related to this product , and sustain reliable end-to-end execution through steady-state operations following potential FDA approval. The Associate Director Oncology...

Our Company is preparing for the potential U.S. launch of an oncology mRNA-based individualized neoantigen therapy for early stage melanoma which involves operational complexities for treatment sites and requires close coordination with cross-functional partners. To ensure site readiness and support consistent site execution, we are building a dedicated team of field-based operational roles to help educate treatment sites on the practical, logistical, and operational requirements necessary to onboard the product effectively, inform treatment sites about helpful workflows and tools related to this product , and sustain reliable end-to-end execution through steady-state operations following potential FDA approval. The Associate Director Oncology...

Our Company is preparing for the potential U.S. launch of an oncology mRNA-based individualized neoantigen therapy for early stage melanoma which involves operational complexities for treatment sites and requires close coordination with cross-functional partners. To ensure site readiness and support consistent site execution, we are building a dedicated team of field-based operational roles to help educate treatment sites on the practical, logistical, and operational requirements necessary to onboard the product effectively, inform treatment sites about helpful workflows and tools related to this product , and sustain reliable end-to-end execution through steady-state operations following potential FDA approval. The Associate Director Oncology...

Our Company is preparing for the potential U.S. launch of an oncology mRNA-based individualized neoantigen therapy for early stage melanoma which involves operational complexities for treatment sites and requires close coordination with cross-functional partners. To ensure site readiness and support consistent site execution, we are building a dedicated team of field-based operational roles to help educate treatment sites on the practical, logistical, and operational requirements necessary to onboard the product effectively, inform treatment sites about helpful workflows and tools related to this product , and sustain reliable end-to-end execution through steady-state operations following potential FDA approval. The Associate Director Oncology...

Global Immunology Marketing is a critical driver of company growth and most importantly significant patient impact – this is an opportunity to join an organization of colleagues with high energy, passion and patient-driven purpose. Under the direction of the VP, Global Immunology Marketing, the Lead Administrative Assistant will provide comprehensive administrative and project management support to the leader and the AVP, Global IBD Immunology Marketing. By leveraging their expertise and skills, the Lead Administrative Associate will ensure seamless coordination and efficient operations across multiple departments. They will contribute to the success of key initiatives by assisting the team in managing...

Our Company is preparing for the potential U.S. launch of an oncology mRNA-based individualized neoantigen therapy for early stage melanoma which involves operational complexities for treatment sites and requires close coordination with cross-functional partners. To ensure site readiness and support consistent site execution, we are building a dedicated team of field-based operational roles to help educate treatment sites on the practical, logistical, and operational requirements necessary to onboard the product effectively, inform treatment sites about helpful workflows and tools related to this product , and sustain reliable end-to-end execution through steady-state operations following potential FDA approval. The Associate Director Oncology...

Our company a global healthcare leader, is currently seeking an Entry-Level Veterinary Associate to join our collaborative, dynamic, and inclusive Laboratory Animal Science Team at the West Point location. The successful candidate will be integral in executing research study tasks, as well as some routine veterinary and animal colony management tasks. On-site and hands-on study-related lab work will be a crucial part of the role. The role also requires rotational weekend work and the ability to apply sound technical skills to assigned tasks, often with minimal supervision. Our company values collaboration, coordination, and communication. We aim to foster an atmosphere...

Our Company is preparing for the potential U.S. launch of an oncology mRNA-based individualized neoantigen therapy for early stage melanoma which involves operational complexities for treatment sites and requires close coordination with cross-functional partners. To ensure site readiness and support consistent site execution, we are building a dedicated team of field-based operational roles to help educate treatment sites on the practical, logistical, and operational requirements necessary to onboard the product effectively, inform treatment sites about helpful workflows and tools related to this product , and sustain reliable end-to-end execution through steady-state operations following potential FDA approval. The Associate Director Oncology...

Our Company is preparing for the potential U.S. launch of an oncology mRNA-based individualized neoantigen therapy for early stage melanoma which involves operational complexities for treatment sites and requires close coordination with cross-functional partners. To ensure site readiness and support consistent site execution, we are building a dedicated team of field-based operational roles to help educate treatment sites on the practical, logistical, and operational requirements necessary to onboard the product effectively, inform treatment sites about helpful workflows and tools related to this product , and sustain reliable end-to-end execution through steady-state operations following potential FDA approval. The Associate Director Oncology...

Our Company is preparing for the potential U.S. launch of an oncology mRNA-based individualized neoantigen therapy for early stage melanoma which involves operational complexities for treatment sites and requires close coordination with cross-functional partners. To ensure site readiness and support consistent site execution, we are building a dedicated team of field-based operational roles to help educate treatment sites on the practical, logistical, and operational requirements necessary to onboard the product effectively, inform treatment sites about helpful workflows and tools related to this product , and sustain reliable end-to-end execution through steady-state operations following potential FDA approval. The Associate Director T...

Our Company is preparing for the potential U.S. launch of an oncology mRNA-based individualized neoantigen therapy for early stage melanoma which involves operational complexities for treatment sites and requires close coordination with cross-functional partners. To ensure site readiness and support consistent site execution, we are building a dedicated team of field-based operational roles to help educate treatment sites on the practical, logistical, and operational requirements necessary to onboard the product effectively, inform treatment sites about helpful workflows and tools related to this product , and sustain reliable end-to-end execution through steady-state operations following potential FDA approval. The Associate Director Oncology...

Our Company is preparing for the potential U.S. launch of an oncology mRNA-based individualized neoantigen therapy for early stage melanoma which involves operational complexities for treatment sites and requires close coordination with cross-functional partners. To ensure site readiness and support consistent site execution, we are building a dedicated team of field-based operational roles to help educate treatment sites on the practical, logistical, and operational requirements necessary to onboard the product effectively, inform treatment sites about helpful workflows and tools related to this product , and sustain reliable end-to-end execution through steady-state operations following potential FDA approval. The Associate Director Oncology...

The role of Associate Director, Global Oncology Communications, is a unique opportunity to join our company, a recognized leader in oncology, as a key member of the Global Oncology Communications team. The role will support the creation and implementation of external communications strategies, plans and tactics related to our company’s broad oncology portfolio and pipeline assets. The candidate selected for this role will work under the guidance of the Executive Director, Global Oncology Communications in a fast-paced and ever-changing environment. The position will be based in Rahway, NJ with a Hybrid setup (combination of 3 days in-office & 2 days...

Our Company is preparing for the potential U.S. launch of an oncology mRNA-based individualized neoantigen therapy for early stage melanoma which involves operational complexities for treatment sites and requires close coordination with cross-functional partners. To ensure site readiness and support consistent site execution, we are building a dedicated team of field-based operational roles to help educate treatment sites on the practical, logistical, and operational requirements necessary to onboard the product effectively, inform treatment sites about helpful workflows and tools related to this product , and sustain reliable end-to-end execution through steady-state operations following potential FDA approval. The Associate Director Oncology...

Our Company is preparing for the potential U.S. launch of an oncology mRNA-based individualized neoantigen therapy for early stage melanoma which involves operational complexities for treatment sites and requires close coordination with cross-functional partners. To ensure site readiness and support consistent site execution, we are building a dedicated team of field-based operational roles to help educate treatment sites on the practical, logistical, and operational requirements necessary to onboard the product effectively, inform treatment sites about helpful workflows and tools related to this product , and sustain reliable end-to-end execution through steady-state operations following potential FDA approval. The Associate Director Oncology...

For over 130 years, we have pioneered groundbreaking science. Today, we are driven by continuous innovation to develop breakthrough medicines, vaccines and technology. Rooted in direct experience on the farm and in the clinic, we work hand in hand with our customers every step of the way. Our singular focus is to empower those who care for animals, helping them manage their vital responsibility with confidence. Because when it comes to animal health, no one sees it like we do. Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety...

Our Company is preparing for the potential U.S. launch of an oncology mRNA-based individualized neoantigen therapy for early stage melanoma which involves operational complexities for treatment sites and requires close coordination with cross-functional partners. To ensure site readiness and support consistent site execution, we are building a dedicated team of field-based operational roles to help educate treatment sites on the practical, logistical, and operational requirements necessary to onboard the product effectively, inform treatment sites about helpful workflows and tools related to this product , and sustain reliable end-to-end execution through steady-state operations following potential FDA approval. The Associate Director Oncology...

Our Company is preparing for the potential U.S. launch of an oncology mRNA-based individualized neoantigen therapy for early stage melanoma which involves operational complexities for treatment sites and requires close coordination with cross-functional partners. To ensure site readiness and support consistent site execution, we are building a dedicated team of field-based operational roles to help educate treatment sites on the practical, logistical, and operational requirements necessary to onboard the product effectively, inform treatment sites about helpful workflows and tools related to this product , and sustain reliable end-to-end execution through steady-state operations following potential FDA approval. The Associate Director Oncology...

We are seeking an experienced and dynamic individual with a strong scientific background and leadership skills to join our launch team as the Regional Cardiovascular Lead Manager. This is an exciting opportunity for a talented, results-driven leader to guide an experienced, high-performing team of representatives who engage scientific and clinical leaders in the cardiovascular market. In this role, you will lead and manage the Regional Cardiovascular Lead team, driving customer engagement strategy and execution within the US Pharma - Chronic Care business. Your primary responsibilities will include supervising the team's activities, shaping executional strategies and engaging with key stakeholders and...

For over 130 years, we have pioneered groundbreaking science. Today, we are driven by continuous innovation to develop breakthrough medicines, vaccines and technology. Rooted in direct experience on the farm and in the clinic, we work hand in hand with our customers every step of the way. Our singular focus is to empower those who care for animals, helping them manage their vital responsibility with confidence. Because when it comes to animal health, no one sees it like we do. Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety...

The Sterile and Packaging Operations Technician is accountable for performing all preventative and corrective maintenance support for formulation, primary filling, inspection, and/or packaging equipment within their area of assignment for the start-up vaccine manufacturing facility at the West Point, Pa Site. This position will also be accountable for providing shop floor operations and environmental monitoring support to their area of assignment. This position will be an individual contributor and member of the Operations team within the Vaccines integrated process team. This will be a hybrid role focused on startup and future routine operation of the pod vaccine manufacturing facility. The...

Our company's Pharmaceutical Sciences organization translates molecules to medicines, working from the discovery interface through registration stability manufacturing by designing, developing and scaling-up the formulation, device, and manufacturing process. Driving drug product design from the bench top to the Good Manufacturing Practice (GMP) manufacturing facilities, our Scientists use cutting edge science to transform drug delivery and manufacturing technology to positively impact patients. The successful candidate will be a passionate Scientist with strong academic fundamentals and a drive to develop new medicines to improve human health. In this role, the individual will be responsible for supporting the formulation development of new...

Role and Responsibilities We are seeking an accomplished scientific leader to join the Quantitative Pharmacology and Pharmacometrics –Oncology (QP2 Oncology) team as Senior Director, Quantitative Systems Pharmacology (QSP). QP2 Oncology is part of the Global Clinical Development organization and has oversight over drug development aspects related to clinical pharmacology, mechanistic PK-PD modeling and pharmacometrics of oncology drugs from post-preclinical candidate (PCC) selection through registration. Our Senior Directors are recognized experts in quantitative drug development and possess a deep, integrated understanding of both the science and the strategic, end-to-end dimensions of oncology drug development. Reporting directly to Executive Director and Section...

Our Company is preparing for the potential U.S. launch of an oncology mRNA-based individualized neoantigen therapy for early stage melanoma which involves operational complexities for treatment sites and requires close coordination with cross-functional partners. To ensure site readiness and support consistent site execution, we are building a dedicated team of field-based operational roles to help educate treatment sites on the practical, logistical, and operational requirements necessary to onboard the product effectively, inform treatment sites about helpful workflows and tools related to this product , and sustain reliable end-to-end execution through steady-state operations following potential FDA approval. The Associate Director Oncology...

The Nonclinical Drug Safety department is seeking a motivated and talented toxicologist to conduct and/or monitor toxicity studies (GLP and non-GLP) as a Study Director or Study Monitor. Toxicologists at our Company are integral members and leaders of collaborative cross functional scientific teams, addressing challenges from early discovery to late development. Our toxicologists provide scientific leadership in the design and overall conduct of in vivo studies and integrate the findings from all contributing scientists into reports that characterize the safety profile of drug candidates. Key Responsibilities Serve as the single point of control (Study Director) on assigned acute through chronic...

The Associate Director, US Oncology Marketing — Lung Scientific Strategy Lead is a high-visibility, high-impact commercial leader responsible for shaping and executing growth-driving initiatives across the Non-Small Cell Lung Cancer (NSCLC) portfolio. This role will lead scientific strategy workstreams supporting inline medication across both early-stage and metastatic indications and will also lead scientific strategy workstreams to support an anticipated new asset launch. You will combine strategic rigor with flawless execution building clear plans, operationalizing them, and driving measurable outcomes. Success requires exceptional stakeholder management, the ability to influence at all levels, and the judgement to balance bold thinking with compliance...

The Director, Portfolio & Resource Operations, Global Data Management and Standards (GDMS) Clinical Data Management (CDM) provides leadership and governance for capacity planning, resource forecasting, and portfolio performance management across CDM. This role drives standardization of metrics, tools, and forecasting processes, ensuring data integrity and actionable insights to enable senior management decision-making. The Director partners cross-functionally and globally to implement enterprise-wide performance tracking and operational review frameworks. Responsibilities Forecasting, Capacity, and Portfolio Management Consolidate functional area inputs to produce reliable demand outlooks; refine allocation algorithms to ensure the Book of Business is delivered on time and to standard. Design, validate,...

For over 130 years, we have pioneered groundbreaking science. Today, we are driven by continuous innovation to develop breakthrough medicines, vaccines and technology. Rooted in direct experience on the farm and in the clinic, we work hand in hand with our customers every step of the way. Our singular focus is to empower those who care for animals, helping them manage their vital responsibility with confidence. Because when it comes to animal health, no one sees it like we do. Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety...

The Future Talent Program features Cooperative (Co-op) education opportunities that last up to 6 months and will include one or more projects. These opportunities in our Manufacturing Division can provide you with great development and a chance to see if we are the right company for your long-term goals. Our vision is to make a difference in the lives of people globally through our innovative medicines, vaccines, and animal health products. We are committed to being the premier, research-intensive biopharmaceutical company and we provide leading innovations and solutions for today and the future. Our core areas of focus in the...

The FLEx Center is a new multi-modality (small molecule, biologics, vaccine) Drug Product development and GMP clinical manufacturing plant in Rahway, New Jersey. The FLEx organization has a mission to enable development of our Company’s pipeline products with speed, agility, and rigor. This mission will be accomplished by 1) Enabling robust formulation and process development with flexible physical and digital infrastructure; 2) Delivering compliant, high quality clinical supplies; 3) Developing talent with a new operating model and promoting a growth mindset. The FLEx organization is seeking a highly motivated individual to serve the role of SAP Manufacturing Systems Specialist. The...

Our Company is preparing for the potential U.S. launch of an oncology mRNA-based individualized neoantigen therapy for early stage melanoma which involves operational complexities for treatment sites and requires close coordination with cross-functional partners. To ensure site readiness and support consistent site execution, we are building a dedicated team of field-based operational roles to help educate treatment sites on the practical, logistical, and operational requirements necessary to onboard the product effectively, inform treatment sites about helpful workflows and tools related to this product , and sustain reliable end-to-end execution through steady-state operations following potential FDA approval. The Associate Director Oncology...

We are seeking a highly motivated and experienced professional to join our team as Associate Director, Commercial Capabilities for our Human Health Learning & Development division. This role offers a global opportunity to shape and execute learning strategies that build the marketing and market access capabilities required to support enterprise current and future launches across Human Health. As the Associate Director, you will be responsible for partnering with US and Global Marketing teams, US and Global Market Access teams, Marketing Excellence & Launch Excellence teams, and GLD teams to identify, prioritize, and address the most critical Marketing and Market Access...

Our Company is preparing for the potential U.S. launch of an oncology mRNA-based individualized neoantigen therapy for early stage melanoma which involves operational complexities for treatment sites and requires close coordination with cross-functional partners. To ensure site readiness and support consistent site execution, we are building a dedicated team of field-based operational roles to help educate treatment sites on the practical, logistical, and operational requirements necessary to onboard the product effectively, inform treatment sites about helpful workflows and tools related to this product , and sustain reliable end-to-end execution through steady-state operations following potential FDA approval. The Associate Director Oncology...

Our Company is preparing for the potential U.S. launch of an oncology mRNA-based individualized neoantigen therapy for early stage melanoma which involves operational complexities for treatment sites and requires close coordination with cross-functional partners. To ensure site readiness and support consistent site execution, we are building a dedicated team of field-based operational roles to help educate treatment sites on the practical, logistical, and operational requirements necessary to onboard the product effectively, inform treatment sites about helpful workflows and tools related to this product , and sustain reliable end-to-end execution through steady-state operations following potential FDA approval. The Associate Director Oncology...

Under the direction of Clinical Data Management and GDMS leadership, the Director, Clinical Data Management Indication Lead, Late Oncology provides operational leadership for data management delivery within an assigned indication(s) for a therapeutic area. The role oversees day-to-day portfolio execution, resource management, and risk and quality oversight to ensure timely, compliant, and high-quality delivery of study and program data. The Director partners cross-functionally across Clinical, BARDS (Biostatistics and Research Data Science), GDIA (Global Data Integration and Automation), and GCDS (Global Clinical Data Standards) to ensure consistent standards application, operational excellence, and capability development within the Therapeutic Area (TA). Responsibilities Own...

Under the direction of leadership, the Associate Director, Portfolio & Resource Operations supports operational excellence through data-driven portfolio and resource analytics. Responsible for maintaining accurate capacity, workload, and utilization data across functions, the role ensures decisions are informed by robust metrics and transparent reporting. Works collaboratively with functional partners to drive standardization and improve visibility into operational performance. Responsibilities Forecasting, Capacity, & Portfolio Management Maintain headcount, workload, and demand models for the functional area; run allocation algorithms to help ensure the Book of Business is delivered with quality and timeliness. Support operating-model optimization within the functional area, translate outcomes into...

Our Company is preparing for the potential U.S. launch of an oncology mRNA-based individualized neoantigen therapy for early stage melanoma which involves operational complexities for treatment sites and requires close coordination with cross-functional partners. To ensure site readiness and support consistent site execution, we are building a dedicated team of field-based operational roles to help educate treatment sites on the practical, logistical, and operational requirements necessary to onboard the product effectively, inform treatment sites about helpful workflows and tools related to this product , and sustain reliable end-to-end execution through steady-state operations following potential FDA approval. The Associate Director Oncology...

The Senior Director, Clinical Data Management Therapeutic Area (TA) Lead, Hematology provides strategic and operational oversight of data management delivery across the assigned therapeutic area(s). The role leads portfolio planning, resource and performance management, and cross-functional alignment to ensure execution against GDMS and enterprise priorities. The Senior Director partners with TA, Geographies (Geo), and Capability Leads to optimize efficiency, standardization, and digital enablement across programs, while driving quality, compliance, and continuous improvement within the TA organization. Responsibilities Accountable for TA (Therapeutic Area) portfolio strategy and prioritization, developing the TA roadmap and study sequencing, and balancing resources, timelines, and risks to...

The Oncology Trainer (OT) supports the U.S. Oncology commercial teams in learning the necessary clinical and sales skills to execute their tasks. They also assist in creating and implementing a yearly training plan to meet learning and business goals. The OT is part of U.S. Oncology Commercial Operations and collaborates with the U.S. Oncology Learning & Development team to provide training solutions at national, regional, district, or individual levels. The OT works with mid-level managers and Directors to understand learning needs and business goals to drive the training needs for field sales. The OT creates and implements learning plans that...

The Quantitative Pharmacology and Pharmacometrics (QP2) Department within our Company’s Research Laboratories in Rahway, NJ, and West Point, PA is excited to welcome a curious, collaborative, and scientifically driven Associate Director to help support our growing cardiometabolic pipelines. In this role, you will represent QP2 on cross-functional teams of experienced scientists working together to discover and advance novel therapeutic agents for cardiometabolic and ophthalmologic diseases. You will contribute to the discovery and development of small molecules, biologics, and non-traditional therapeutics, including peptides, novel biological constructs, and other emerging modalities. The successful candidate will be a skilled quantitative drug developer with...

Our Company is preparing for the potential U.S. launch of an oncology mRNA-based individualized neoantigen therapy for early stage melanoma which involves operational complexities for treatment sites and requires close coordination with cross-functional partners. To ensure site readiness and support consistent site execution, we are building a dedicated team of field-based operational roles to help educate treatment sites on the practical, logistical, and operational requirements necessary to onboard the product effectively, inform treatment sites about helpful workflows and tools related to this product , and sustain reliable end-to-end execution through steady-state operations following potential FDA approval. The Associate Director Oncology...

Bio Process Operations Technician (2nd shift) The Bio Process Operations Technician will be a member of the Maintenance & Operations team within the Vaccines integrated process team for a start-up vaccine manufacturing facility in Wilson, NC. This person is accountable for providing shop floor operations support to aseptic manufacturing within the vaccine manufacturing facility. Tasks will include aseptic primary filling, inspection, packaging, and CIP/SIP. This position will also perform various roles to include executing routine room and equipment disinfection as well as managing the movement of gowning, disinfectants, and materials. In addition to supporting operations activities, the role will be...

Bio Process Operations Technician (2nd shift) The Bio Process Operations Technician will be a member of the Maintenance & Operations team within the Vaccines integrated process team for a start-up vaccine manufacturing facility in Wilson, NC. This person is accountable for providing shop floor operations support to aseptic manufacturing within the vaccine manufacturing facility. Tasks will include aseptic primary filling, inspection, packaging, and CIP/SIP. This position will also perform various roles to include executing routine room and equipment disinfection as well as managing the movement of gowning, disinfectants, and materials. In addition to supporting operations activities, the role will be...

As a Cardiovascular Disease Specialist, you will drive meaningful patient impact by leveraging our scientific expertise and serving as the primary contact for customers within your assigned territory. As a key member of the local Customer Team, you will collaborate closely with Account Executives, Integrated Delivery Systems leaders, and other field colleagues to deliver seamless, patient-focused solutions. Territory Assignment This is a field-based sales role responsible for covering the St. Louis, MO territory and surrounding areas. Travel (%) depends on the needs of the territory and where the selected candidate resides, and overnight travel may be required about 25% of...

Specialist, Materials Management Location Rahway, New Jersey Department Pharmaceutical Operations and Clinical Supply Position Overview Join us at the forefront of pharmaceutical innovation. The FLEx Center is a state-of-the-art, multi-modality Drug Product development and GMP clinical manufacturing facility dedicated to advancing small molecules, biologics, and vaccines. We are seeking a dynamic Specialist, Materials Management who is passionate about optimizing processes and driving efficiency in a fast-paced environment. This role plays a pivotal part in ensuring materials flow seamlessly through the site, enabling groundbreaking drug development and manufacturing operations. Key Responsibilities Champion Just-in-Time (JIT) Practices Execute JIT warehousing strategies to maximize...

The Associate Director, Patient and Channel Data Management will report into Director, Commercial Data Solutions within the Data Strategy products and Innovation organization (DSPI) department. In this role, a typical day might include The Associate Director, Patient and Channel Data management is responsible for the curation, governance, quality and operationalization of patient/specialty data assets that power commercial decision making across therapeutic areas. The ideal candidate brings deep expertise in specialty pharmaceutical data ecosystems, strong problem-solving capabilities, and the ability to influence and drive alignment across a broad set of cross-functional partners. This role might be for you if you can/have...

Our Senior Territory Representatives interact face to face with our customers, understand their needs and consult to offer the right solutions. We work collaboratively in field sales teams and play a critical role in supporting our customer centric business model. This position is responsible for working in their respective territory to understand and identify veterinary clinic, shelter facility, and corporate account customer needs, by selling our Company's Animal Health (AH) division, Companion Animal product portfolio, supporting pull-through activities relative to the customer strategy, and ensuring that our Company's Animal Health division is viewed as bringing value and technical innovations aligned...

Our company is a global healthcare leader with a diversified portfolio of prescription medicines, vaccines, and animal health products. We are recognized as an industry leader in immuno-oncology (IO) and vaccines discovery and development. For more than a century, our company has translated scientific innovation into medicines and vaccines that improve and save lives worldwide—anchored in ethical integrity, scientific excellence, and a clear mission to transform global health. Role Overview We are seeking an experienced talented scientist to join the Quantitative Pharmacology and Pharmacometrics – Immune/Oncology (QP2-IO) team in the role of Associate Director QP2-IO team is part of...

As our company accelerates its adoption of artificial intelligence, we are evolving into an organization powered by intelligent products, agentic workflows, and agile teams. To deliver measurable business value, we are modernizing the digital marketing ecosystem that connects customer knowledge, journey orchestration, personalization, and channel activation to create relevant, compliant, and measurable customer experiences at scale. The Executive Director, Digital Marketing Platforms is a senior leadership role within Digital Human Health (DHH) / Digital Content & Customer Experience Capabilities (DCCE) team. This leader will define the product strategy and lead the portfolio of digital marketing platforms and capabilities spanning customer...

This role will reside within the DHH US Market Engagement Team for Pharma. This team provided strategic thought-partnership to US commercial stakeholders through understanding brand strategy, co-creating DHH demand and associated business requirements aligned to business priorities. The US Market Engagement team Quarterbacks demand fulfillment and leads the activation of DHH products and services. The Associate Director, US Market Engagement, Data Science & Advanced Analytics, will be responsible for developing data-driven insights to inform brand strategy and tactics in support of the pharma portfolio. This role will focus on applying advanced data science to deliver strategic non-product DHH services to...

We are seeking a Growth and Improvement minded Regional Medical Scientific Director (aka Medical Science Liaison, MSL) in Respiratory - COPD that can help drive our Strategic Operating Priorities. Summary, Focus and Purpose The Regional Medical Scientific Director (Medical Science Liaison) is a credentialed (i.e., PhD, PharmD, DNP, MD) Director Level Medical Affairs position and therapeutic and disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs). The role provides balanced, factual, scientific information about non-product areas of interest to the Company and replies to scientific questions from SLs, including questions about Company products....

Within Digital Manufacturing and the laboratory domain, this Director will lead the product strategy, experience, implementation, and value realization of a global laboratory digital platform. The role will connect opportunities across Research, Development, Manufacturing, Quality, and IT, translating shared needs and emerging possibilities into a coherent roadmap, scalable capabilities, and meaningful improvements in laboratory work . By making laboratory information more accessible, connected, and contextualized, the platform will strengthen results interpretation, reporting, analytics, and data-informed decision-making across the laboratory network. The Director will combine established product ownership capabilities, strong technology acumen, and an entrepreneurial, outside-in perspective. Drawing on experience from...

The Formulation, Laboratory, and Experimentation (FLEx) Center in Rahway, New Jersey, includes a cutting-edge sterile drug product cGMP clinical supply manufacturing facility, known as FLEx Sterile, which is currently in the operational start-up phase. FLEx Sterile is positioned to play a pivotal role in delivering our clinical pipeline to patients worldwide, supporting a various range of product modalities including sterile small molecules, biologics, vaccines, and antibody-drug conjugates (ADCs). The facility supports the formulation and filling of clinical and developmental sterile products for critical program needs, such as new products in process development, products undergoing scale-up, launch and transfer to the...

As a Cardiovascular Disease Specialist, you will drive meaningful patient impact by leveraging our scientific expertise and serving as the primary contact for customers within your assigned territory. As a key member of the local Customer Team, you will collaborate closely with Account Executives, Integrated Delivery Systems leaders, and other field colleagues to deliver seamless, patient-focused solutions. Territory Assignment This is a field-based sales role responsible for Terre Haute, Indiana covering Bloomington, IN, Terre Haute, IN, Greenwood, IN, Columbus, IN, Franklin, IN and surrounding areas. Travel percentage depends on the needs of the territory and where the selected candidate resides,...

Our company is a global healthcare leader with a diversified portfolio of prescription medicines, vaccines, and animal health products. We are recognized as an industry leader in immuno-oncology (IO) and vaccines discovery and development. For more than a century, our company has translated scientific innovation into medicines and vaccines that improve and save lives worldwide—anchored in ethical integrity, scientific excellence, and a clear mission to transform global health. Role Overview The Quantitative Pharmacology and Pharmacometrics – Immune/Oncology (QP2-IO) Department of our Company's Research Laboratories is seeking a curious and collaborative Senior Scientist to support our rapidly expanding oncology pipelines....

Associate Principal Scientist, Regulatory CMC Digital Innovation Rahway, NJ or West Point, PA Our Company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity, knowledge, imagination, skill and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement, and teamwork. As part of our global team, you’ll have the...

Grow and accelerate your career with our Oncology Sales organization and join a team that’s driven to make an impact on cancer patients! We take a customer-centric approach by leveraging emerging digital technologies and data analytics to better understand our patients' needs. Developing your career with us will allow you to join a group of passionate professionals, driven by purpose and determined to help save and improve lives. Help us continue to grow and define the oncology market of today and tomorrow with a driven, customer-focused, and collaborative team. As an Oncology Sales Representative, you will be a key member...

Role Summary The Payer and Health Systems Oncology Precision Medicine Medical Affairs Director (PHSO PM MAD) is a diagnostic, therapeutic and disease expert who develops ongoing professional relationships with healthcare decision makers across reference laboratories, managed markets organizations including laboratory benefit managers, integrated delivery networks, oncology pathway organizations, oncology group purchasing organizations, federal government payers and health systems and state oncology/hematology societies. The PHSO PM MAD provides accurate information across the full oncology product portfolio, precision medicine, clinical science, and quality management in a balanced and credible manner consistent with the regulatory environment and the company’s ethical standards. This role...

The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Oncology therapeutic area, specifically in our Hematology Section. Travel on company business about twenty (20) percent of the time to manage future or ongoing clinical research projects. Education M.D or M.D./Ph.D. Required Experience and Skills Must have experience in industry or senior faculty in academia. Minimum of 3 years of clinical medicine experience. Minimum of 1 year of industry experience in drug development or biomedical research experience in academia. Demonstrated record of scientific scholarship and achievement. Proven...

CALLING FUTURE MANUFACTURING LEADERS The Manufacturing Leadership Development Program (MLDP) is our flagship global manufacturing graduate program. Our simple objective is to identify, hire, and develop our future Manufacturing Leaders. If you are passionate about launching a career in manufacturing, then we are eager to engage with you, focus on your development, and bring greater value to our patients worldwide. Over the 3-year rotation program, we will invest in your development, giving you exposure and experience across our business and preparing you for a role in leadership. The program will provide experiential and formal learning opportunities to build the technical...

Our Company is seeking creative chemists for positions within the Discovery Chemistry Department. The successful candidate will join multidisciplinary, highly collaborative discovery teams to invent novel medicines by applying innovative synthetic chemistry, analytical techniques, and data analysis to design and synthesize drug candidates and intermediates. Additionally, you will have the opportunity to expand your knowledge and skills through collaborations with talented and dedicated colleagues while advancing your career. Specific responsibilities will include the following Act as an expert in the laboratory, executing on program and chemistry strategy. Develop and utilize innovative synthetic, medicinal chemistry and/or chemical biology problem solving skills...

We are seeking an accomplished scientific leader to join the Quantitative Pharmacology and Pharmacometrics – Immuno-Oncology (QP2‑IO) team as Senior Director , Advanced Pharmacometrics. QP2‑IO is part of the Global Clinical Development organization and is responsible for clinical pharmacology and pharmacometrics strategy and execution for oncology assets, from candidate nomination through registration. Our Senior Directors are recognized experts in quantitative drug development and possess a deep, integrated understanding of both the science and the strategic, end‑to‑end dimensions of oncology drug development. Reporting directly to Executive Director and Section Head, QP2‑IO, the Senior Director will lead advanced pharmacometrics strategy and implementation...

As a Cardiovascular Disease Specialist, you will drive meaningful patient impact by leveraging our scientific expertise and serving as the primary contact for customers within your assigned territory. As a key member of the local Customer Team, you will collaborate closely with Account Executives, Integrated Delivery Systems leaders, and other field colleagues to deliver seamless, patient-focused solutions. Territory Assignment his is a field-based sales role responsible for the Knoxville, TN territory covering Knoxville- Maryville, Alcoa, Seymour, Morristown, New Tazewell, Greenville, Erwin, Sevierville, Newport, Johnson City, Jefferson City and surrounding areas. Travel (%) depends on the needs of the territory and...

Our Finance team brings together our financial perspectives into our overall strategic and tactical decision making. We use state-of-the-art techniques for financial analysis, planning, accounting, reporting, and performance evaluation. This allows the organization to continue advancing medical innovation and improve lives. Position The Associate Director – International Tax will report directly to the Director, Tax Planning, located in Rahway, NJ. Responsibilities will include, but not limited to Support cross-border structuring and tax planning initiatives by modeling the impact of proposed transactions, business initiatives, and legislative or regulatory changes on the Company's effective tax rate. Assist with dividend planning opportunities...

Technician, Operations Pharmaceutical Operations and Clinical Supply is seeking highly motivated individuals for R&D Operations roles in our Rahway, NJ, Formulation, Laboratory, and Experimentation (FLEx) Center to support drug product development and GMP clinical supply of oral solid dosage, sterile, and specialty dosage forms. Positions will support development and clinical manufacturing and supply, as part of the FLEx-Sterile, FLEx-OSD, or RY119 team. This position will be responsible for hands-on processing activities that include room setup, equipment and material preparation, equipment assembly and disassembly, cleaning, and processing of raw materials into finished drug product. These individuals are expected to partner with...

This position drives scientific planning, strategy, and execution of Phase 1-4 clinical studies. Under the direction of the Program Lead, you will collaborate with global cross ­functional team members including clinical directors and study managers to lead/support clinical trial scientific activities. Job Responsibilities Responsible for the clinical/scientific execution of clinical protocol(s). Serves as the lead clinical scientist on the clinical trial team. Collaborates with the Medical Writer on clinical/scientific and regulatory documents. Partners with Study Manager on study deliverables. Participates in the set up and design during study start up (e.g., database set up) Lead medical monitoring team in review...

The Associate Director, Production Operations serves as the Production Lead for FLEx Non-Sterile operations and is accountable for end-to-end manufacturing readiness, production scheduling, and execution across both first and second shift operations. This role provides direct leadership for production teams and is responsible for ensuring safe, compliant, and reliable execution of manufacturing campaigns while balancing customer demand, resource utilization, and operational efficiency. The Production Lead partners closely with Tech Ops Engineering, Process Engineering, Quality, Supply Chain, Maintenance, and Program teams to ensure that manufacturing plans are executable and that production commitments are delivered on time. This role owns daily manufacturing...

AD, Primary Market Research Focus Area Infectious Diseases with a primary focus on HIV Our Marketing team is passionate about bringing our medicines and vaccines to our customers around the world. Through digital listening and patient analytics, we can understand our customers’ needs and strive to provide solutions to meet them. At We are seeking those who have a passion for using strategic insights, data and analytics to drive decision making, that will allow us to tackle some of the world’s greatest health threats. Within our commercial Insights, Analytics, and Data organization we are transforming to better power decision-making...

Our Company's Audit and Assurance Services The primary purpose of Audit and Assurance Services is to provide value-added independent and risk-based audit and assurance services. Position Overview / Function and Responsibility Under the direction of the Client Audit Director ("CAD") and the Auditor-in-Charge ("AIC"), the Specialist will Participate in the execution of financial, operational, SOX 404, and IT audits, integrated audits, and process audits, both domestically and internationally, to help ensure a strong internal control environment is maintained across the Company. Partner with MCAAS colleagues, clients, and other organizations to effectively complete assigned audit activities. Execute audit procedures and prepare...

The Senior Specialist of Automation serves as the BAS/HVAC technical authority for West Point, GWES Southeast Pennsylvania. The senior specialist is responsible for automation system performance, compliance, reliability, energy optimization, and lifecycle management. The position provides technical leadership to specialists and technicians while leading capital projects, managing change controls, supporting audits, and maintaining BAS systems in a state of GMP compliance. Key Responsibilities Leadership Lead cross-functional collaboration between GWES, Utilities, Maintenance, Quality, our Research & Development division, our Manufacturing division, and IT. Provide technical direction to EUTS Specialists and technicians. Lead investigations and resolution of systemic BAS/HVAC issues. Manage automation...

Our Company is currently seeking an exceptional chemist to join the Discovery Process Chemistry group located at our Boston, MA site. This role offers the opportunity to join a vibrant group of innovative laboratory scientists with broad impacts across our late discovery and early development portfolios. Core responsibilities include the development of innovative solutions to complex chemistry problems across a portfolio of projects in the discovery phase, from lead identification through candidate selection. A successful candidate is expected to apply cutting edge methodologies to synthetic route design in order to enable medicinal chemistry research and accelerate the delivery of target...

Technical expert with demonstrated expertise in PLC Programming & Troubleshooting, HMI Development & Support, Robotics, Machine Vision, Industrial Networks, SDLC/CSV, Change Control, GMP Documentation, Root Cause Analysis and Continuous Improvement. Automation & Controls Engineering · Provide technical support for industrial automation systems supporting manufacturing and packaging operations. · Troubleshoot and optimize PLCs, HMIs, robotics, machine vision systems, motion control and servo-driven equipment. · Lead root cause analysis and implement sustainable corrective actions. · Support integration of new equipment and emerging automation technologies. Digital Manufacturing · Support serialization, aggregation, SAP ATTP and track-and-trace solutions. · Drive data integrity, cybersecurity and digital...

Our Manufacturing Operations teams are the people that make therapies for our patients. We work in the manufacturing plants with a “Safety First, Quality Always” mindset, striving for continuous improvement, and earn our right to produce. We work in local plants connected to our global manufacturing network supplying the highest quality of raw materials, intermediates, and finished products. Our ability to excel depends on the integrity, knowledge, imagination, skill, , and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement, and teamwork. As part of our global team, you’ll have the...

Principal Scientist (Director) in Translational Medicine-Oncology Translational Medicine at our Research Division is responsible for early clinical development of novel therapeutics, working in close collaboration with Discovery Sciences and late-stage Clinical Research. We work with all therapeutic areas within our Research Division. We are seeking a highly qualified individual for a position in our group. Candidates must have a strong background in basic and/or clinical translational research and a desire to work collaboratively across different therapeutic areas. Translational Medicine is specifically responsible for Leadership of the early clinical development strategy for novel therapy programs from Preclinical Candidate approval through Clinical...

The Pharmaceutical Analysis & Digital Technologies (PADT) Analytical Capabilities & Operations (ACO) department of our Research and Development Division is seeking applicants for a Metrology and Validation Specialist position available at the Rahway, New Jersey research facility. The Metrology and Validation Specialist will work as part of the integrated US Metrology and Validation team and drive a culture of quality and operational excellence across the global Development Sciences & Clinical Supply (DSCS) network. The role oversees and supports the onboarding, qualification, validation, and routine maintenance of analytical equipment and instrumentation within a GMP environment. The key responsibilities of this role...

Under the guidance of the Director, Financial Planning and Analysis in the Human Health (HH) Finance Center of Excellence (CoE), this position is primarily responsible for the reporting and analysis of the consolidated HH commercial business. The Associate Director will provide operational and analytical support to ensure the integrity of divisional forecasts, Budgets and Long-Range Operating Plans (LROP) and will develop presentation materials for senior leadership. There will also be an opportunity to support HH operational and strategic initiatives, finance initiatives, and various HH senior management requests, enabling the candidate to obtain broad exposure to the commercial operations. In performing...

The Executive Director (Distinguished Scientist) and Product Development Team (PDT) lead has primary responsibility for the planning and directing of clinical research activities involving new or marketed medicines in the Oncology therapeutic area, Hematology section. The Executive Director will manage and oversee the entire cycle of late-stage clinical development from Phase 2 to Phase 5, including development of program strategy and design, protocol authoring, initiation, execution, monitoring, analysis, regulatory reporting, publication, and presentation at national and international meetings. They will lead cross-functional product development teams that oversee program strategy and execution, will provide internal scientific leadership for cross-functional areas supporting...

The Pharmaceutical Analysis & Digital Technologies (PADT) External Capabilities, Validation, and Compliance (ECVC) department of our company Research Laboratories Division is seeking applicants for a Validation Specialist position available at either the Rahway, New Jersey research facilities. The Analytical Instrument Validation Specialist will work as part of the integrated Validation and Compliance team and drive a culture of quality and operational excellence across the global Development Sciences & Clinical Supply (DSCS) network. The Analytical Instrument Validation Specialist role oversees and/or supports the validation of novel computerized analytical instrumentation within the GMP environment for multiple sites (Pennsylvania, New Jersey, and Schachen,...

The Quantitative Pharmacology and Pharmacometrics (QP2) Department of our Company's Research Laboratories in West Point, PA / Rahway, NJ is seeking a curious and collaborative Senior Scientist to support our rapidly expanding cardiometabolic and ophthalmology pipelines. As a senior specialist you will be part of a cross-functional teams of experienced scientists to discover and develop novel therapeutic agents of various modalities for cardiometabolic and ophthalmic diseases. The senior specialist is a skilled quantitative scientist, with a good understanding of the strategic elements of drug discovery and development. The senior specialist should demonstrate collaborative work spirit and good communication skills. Within...

In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our Company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health. Responsibilities This position supports statistical programming activities for late-stage drug/vaccine clinical development projects. This may include leadership of one or more projects. Accountability predominantly includes the development and execution of statistical analysis and reporting deliverables (e.g. safety and efficacy analysis datasets,...

Role Summary The Principal Scientist/Director, Value & Implementation (V&I) Outcomes Research, position resides in the V&I organization, which includes Global Medical and Scientific Affairs as well as Outcomes Research. Under the guidance of a senior leader, this position supports value evidence outcomes research plans and real-world evidence activities for pipeline products to meet the value evidence needs of clinicians, payers, policymakers, health technology assessment (HTA)/reimbursement agencies and health systems globally. Types of studies executed include prospective and retrospective observational studies to characterize disease burden and epidemiology, treatment patterns, health-care resource utilization and costs, physician and patient satisfaction surveys, clinical and...

The Executive Director, Center for Scientific Exchange Excellence (ED CSEE), position resides in the Value & Implementation (V&I) organization, which includes Global Medical and Scientific Affairs (GMSA), Global Medical and Value Capabilities (V&I GMVC), as well as Outcomes Research. This position is a leadership role within V&I GMVC that reports directly to the Vice President, V&I GMVC Lead. The ED CSEE is an integral member of the V&I GMVC Leadership Team providing insight and advice on strategic direction and is accountable for assisting and driving execution of the vision of V&I GMVC and CSEE. This position oversees the CSEE team,...

At Responsibilities Work within the Medical Affairs organization to identify, establish, and manage collaborative professional relationships with community-based scientific leaders (SLs) and healthcare providers. Conduct peer-level scientific discussions and maintain a reliable presence to ensure SLs have a Medical Affairs contact within our company. Engage in proactive non-product discussions regarding scientific issues to understand real-world prevention gaps, persistent disparities, and barriers to uptake across various care settings. Facilitate appropriate scientific exchange of information with SLs, including integration of scientific knowledge with actionable insights to inform our Company's research, development and strategies. Communicate external stakeholder opinions, insights, and feedback on...

Electrician (Hourly - RY-USW Union Represented Position) Are you looking for an exciting opportunity with a rapidly growing pharmaceutical manufacturer? If so, then this is the opportunity for you! Under general supervision and planning and engineering support, the Electrician will install, operate, maintain, alter, troubleshoot and repair electrical power and lighting distribution systems along with a wide variety of industrial electrical equipment. Demonstrate ownership of equipment systems serviced and pride in quality work. · Install, inspect, troubleshoot, repair, maintain or alter electrical services, equipment and controls, using approved and properly sized wire, conduit, raceways and equipment. · Work with high...

We are seeking an experienced talented scientist to join the Quantitative Pharmacology and Pharmacometrics – Immune/Oncology (QP2-IO) team in the role of Director. QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects related to clinical pharmacology and pharmacometrics of oncology drugs from post-PCC to registration. Directors are leaders in the field of quantitative drug development, with a strong, integrated understanding of the strategic elements of drug development. As a subject matter expert, the Director within the QP2-IO Group will work closely with teams of highly collaborative, cross-functional scientists to contribute to development...

Director, Field Enablement Planning & Execution Role Summary With direct ownership and oversight into the field enablement planning & execution function of Strategy & Field Enablement, this leader will be responsible for the development, execution, and governance of end-to-end field enablement planning and execution, including accelerated and multi‑indication launches, large‑scale field structure transformations field readiness efforts, and other field-related initiative. The Director will proactively manage complexity across headquarters functions, establish the operating model and standards for field readiness, and ensure a seamless operational experience for field sales and account management teams by driving timely decision-making, resolving cross-functional constraints, and ensuring...

The Biologics Process Research & Development organization within our Company Research Labs is responsible for developing the drug substance manufacturing processes for our Company's biologics pipeline. We work closely with colleagues in Discovery, Pre-clinical, and Early Development to rapidly develop processes for different biotherapeutics and efficiently produce material to supply clinical trials. We are also responsible for commercial process development, and development and implementation of new technologies. We work with our partners in our Company Manufacturing Division to commercialize and launch new products. This role will support the Next Generation Biologics (NGB) facility, which will be a premier, state-of-the-art facility,...

Associate Principal Scientist, Statistical Programming – Rahway, NJ Provide high quality statistical programming analysis and reporting deliverables for global PK modeling and simulation stakeholders Oncology therapeutic area. Gather and interpret user requirements, retrieve the required data, transform the data into modeling-ready analysis datasets, and develop tables and figures according to the modeling analysis plans. Lead the data stewardship and take accountability for the creation of modeling data from original data source(s) to final modeling dataset. Act as a key collaborator with modelers, statisticians and other project stakeholders and execute project plans efficiently and oversee the work of other team members...

We aspire to be the premier research-intensive biopharmaceutical company. We're at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. Join our team and be part of a mission-driven organization that uses the power of leading-edge science to save and improve lives around the world. This role serves as an essential part of the External Manufacturing & Network Equipment team, in providing technical leadership and support to our company's internal & external packaging network, focusing on developing and executing packaging and device assembly equipment and processes including packaging...

The department of Pharmacokinetics, Dynamics, Metabolism & Bioanalytics (PDMB) is seeking a curious and collaborative Senior Scientist for our growing Translational PK/PD organization. The Translational PK/PD Senior Scientist is a skilled mathematical modeler and scientist who designs and executes analyses, with supervision, guiding drug discovery strategy with a focus on biologics, protein therapeutics, and peptides. The Translational PK/PD Senior Senior Scientist will Serve as PK/PD modeler in cross-functional teams, to make model-informed decisions about drug discovery, modality selection, and dose prediction across therapeutic areas; Integrate in vitro and in vivo data to build PKPD, PBPK, quantitative systems pharmacology (QSP), or...

Join the Rahway, NJ Animal Health Team Our Company's Global Animal Health Research & Development (R&D) division is a pioneer in the discovery, development and registration of vaccines and therapeutics for animals.. To strengthen our team, we are looking for a highly skilled and motivated Principal Scientist to join our R&D team. Purpose of the Role The Principal Scientist, Drug Discovery in our Research and Development Department will be responsible for identifying new molecular entities and technologies for use in animal health from our Company Laboratories or from external partners such as human pharma or biotech companies as well as...

The Formulation, Laboratory, and Experimentation (FLEx) Center in Rahway, New Jersey, features a cutting-edge sterile drug product cGMP clinical supply manufacturing facility, known as FLEx Sterile. The FLEx Sterile facility is poised to play a pivotal role in the long-term success of delivering our clinical pipeline to patients worldwide, encompassing a diverse range of product modalities, including sterile small molecules, biologics, vaccines, and antibody-drug conjugates (ADCs). The FLEx organization has a mission to enable development of our Company’s pipeline products with speed, agility, and rigor. This mission will be accomplished by 1) Enabling robust formulation and process development with flexible...

Associate Director, Facilities Operations & Integrated Services Wilmington Biologics Site The Associate Director, Facilities Operations & Integrated Services is responsible for the strategic leadership, operational excellence, and compliance of all non-engineering facility operations supporting the Wilmington Biologics campus. Reporting to the Director of Engineering, Maintenance & Utilities (EMU), this leader oversees Integrated Facilities Management (IFM), soft services, vendor management, laboratory and logistics building support, workplace services, landlord relations, and facility operations that enable safe, compliant, and efficient business operations. Facilities Operations Leadership Lead all site Facilities Operations supporting laboratories, logistics buildings, offices, warehouses, and administrative facilities. Develop long-term facilities...

Associate Director – Global Engineering Solutions Our Engineers support internal and external manufacturing operations remain operational, continuously improve and innovate. With our extensive range of facilities and environments, our Engineers have opportunities across many diverse areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation. Global Engineering Solutions (GES) executes a wide variety of capital and expense projects to ensure that our company has the capabilities and facilities to meet our goal to provide World Class Supply of Medicines . The GES group is seeking an Associate Director of Engineering to manage large capital...

The Senior Specialist will work closely with US Commercial teams as a key financial and strategic business partner to support the goals and growth of our Company's Human Health business. The Senior Specialist is responsible for forecasting, month-end close, budgeting, and financial evaluation activity for the financial base within their scope of responsibility. The Senior Specialist partners closely with cross functional teams, including finance, marketing, Integrated Account Management, market access, customer contract management, government pricing, IT, legal, compliance, audit and corporate teams to evaluate business performance and identify, evaluate and execute strategic opportunities. The Senior Specialist will develop a deep...

As part of our company's Vaccine Manufacturing Organization, the Durham team is seeking a highly motivated individual to serve as a Senior Operations Specialist within the Operations Manufacturing Support team. In this role, you must be able to work efficiently in a fast-paced environment and be hands-on when called for by the situation. This role requires the ability to distill large quantities of complex data into simplified reporting and actionable measures, strong problem-solving skills, rapid disciplined decisions and prioritization of work. The position must also demonstrate strong collaboration and communication skills to enable interfacing with both internal contacts (site level)...

Director, Cheminformatics – Modeling & Informatics The successful candidate will bring exceptional matrix leadership and managerial skills to drive cheminformatics and data science innovation that amplifies pipeline impact across our discovery organization. They will lead a team of highly skilled cheminformatics professionals and create an environment that supports the growth of data science talent through sustained engagement with stakeholders in chemistry, biology, and IT. In this role, the candidate will guide the development and application of cheminformatics capabilities that enable and enhance decision-making across the drug discovery process. The team serves as a force multiplier—translating key scientific questions into scalable...

Patent Attorney Are you interested in the intersection of scientific innovation and property law, especially how to efficiently capture innovation with intellectual property, incentivize continued R&D and drive access to life-saving medicines for patients? If so, the Patent Counsel role at our Company could be an ideal opportunity for you. We are looking for a highly motivated and skilled individual to join our team in Rahway, New Jersey. In this role, you will work directly with our internal R&D team to identify inventions, conduct patentability assessments, and draft and prosecute patent applications for novel chemical sciences inventions. The position will...

The department of Pharmacokinetics, Dynamics, Metabolism & Bioanalytics (PDMB) is seeking a curious and collaborative Scientific Associate Director for our growing Translational PK/PD organization. The Translational PK/PD Associate Director is an expert mathematical modeler and scientist who independently designs and executes analyses with minimal supervision, guiding drug discovery strategy with a focus on biologics, protein therapeutics, and peptides. The Translational PK/PD Scientific Associate Director will Serve as expert PK/PD modeler in cross-functional teams, to make model-informed decisions about drug discovery, modality selection, and dose prediction across therapeutic areas; Integrate in vitro and in vivo data to build PKPD, PBPK, quantitative...

The Process Chemistry organization located at our Rahway, NJ site is seeking highly motivated and exceptional chemists who are looking for an opportunity to work in a fast-paced environment that provides a high degree of technical responsibility. A successful candidate will be joining a vibrant group of innovative scientists with broad deliverables ranging from the design of clinical supply routes for drug candidates to driving innovative solutions to complex chemistry problems in the discovery phase. As a process team member, this role will focus on the design and development of efficient, scalable manufacturing routes and clinical supply processes for multi‑modality...

The Drug Metabolism and Pharmacokinetics (DMPK) group within the PDMB function is seeking a highly motivated, collaborative scientist to support mass spectrometry-based immunogenicity assessment. The successful candidate will contribute to the execution of MHC-Associated Peptide Proteomics (MAPPs) studies and related LC-MS workflows used to characterize antigen presentation and support biologics, conjugates and peptides programs. The ideal candidate will primarily perform laboratory-based activities and be responsible for executing cell-based and immunoaffinity workflows, preparing samples for LC-MS analysis, maintaining laboratory instrumentation, and generating high-quality experimental data. The candidate will work in a multidisciplinary environment alongside scientists in immunology, bioanalysis, and mass spectrometry...

Serves as the day-to-day bridge between brand teams and the Patient Support CoE for assigned therapeutic areas, owning TA-specific insight generation, patient journey mapping, and implementation support for critical capabilities. Accountable for translating designs and patient-facing capability concepts into operational and scalable solutions — ensuring new capabilities fit into the broader architecture or new capabilities deploy without disrupting live patient support operations. Key Responsibilities Understand and pressure test TA-specific patient support designs , including workflow assumptions, operational feasibility, and implementation sequencing Serve as day-to-day bridge between brand and CoE teams , enabling integration and one-voice execution across assigned TA Support...

Principal Scientist, DSCS Digital Technologies-Laboratory Automation, Digital Lab and Automation Strategy We are seeking a Principal Scientist to join our DSCS Digital Technologies (DDT) organization, within Development Sciences and Clinical Supply (DSCS), located in Rahway, NJ. Primary Responsibilities We are a global biopharmaceutical leader with a portfolio of prescription medicines, oncology, vaccines and animal health products. We are driven by our purpose to develop and deliver innovative products that save and improve lives. With 69,000 employees operating in more than 140 countries, we offer state-of-the-art laboratories, plants and offices that are designed to inspire our employees as we learn, develop...

Are you passionate about leveraging technology to drive business success? Join our company, a premier research-intensive biopharmaceutical company, as an IT/OT Business Analyst in our Global Animal Health Manufacturing IT division. In this role, you will be at the forefront of innovative health solutions, advancing the prevention and treatment of diseases in people and animals. If you are eager to make a significant impact and thrive in a dynamic environment, we want to hear from you. We offer relocation assistance for qualified candidates. Responsibilities Plan, monitor, organize, and oversee IT/OT projects. Support and configure software & hardware, ensuring appropriate support...

Serves as the day-to-day bridge between brand teams and the Patient Support CoE for assigned therapeutic areas, owning TA-specific insight generation, patient journey mapping, and implementation support for critical capabilities. Accountable for translating designs and patient-facing capability concepts into operational and scalable solutions — ensuring new capabilities fit into the broader architecture or new capabilities deploy without disrupting live patient support operations. Key Responsibilities Understand and pressure test TA-specific patient support designs , including workflow assumptions, operational feasibility, and implementation sequencing Serve as day-to-day bridge between brand and CoE teams , enabling integration and one-voice execution across assigned TA Support...

Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us. Animal Health Global Supplier Management is an organization of approximately two hundred professionals with the common objective of compliant, competitive, and innovative acquisition of goods & services from leading suppliers and partners that deliver a competitive advantage. Our company manages approximately $1.2B of third party spend through an organizational...

The Director, Global Oncology Market Access - Alliances, will report to the Executive Director, oGMAx Alliances and lead global access and pricing strategy development and execution for new oncology pipeline assets across multiple indications. The role requires oncology market knowledge, understanding of the evolving global payer environment, and experience in market access, pricing, health outcomes, and launch preparation. The candidate must have strong project coordination, communication, and collaboration skills to lead cross-functional initiatives with commercial, clinical, regulatory, evidence generation, medical affairs, regional/local Access teams, and external alliance partners, while following established ways of working and legal/compliance requirements. Key deliverables include...

Serves as the day-to-day bridge between brand teams and the Patient Support CoE for assigned therapeutic areas, owning TA-specific insight generation, patient journey mapping, and implementation support for critical capabilities. Accountable for translating designs and patient-facing capability concepts into operational and scalable solutions — ensuring new capabilities fit into the broader architecture or new capabilities deploy without disrupting live patient support operations. Key Responsibilities Understand and pressure test TA-specific patient support designs , including workflow assumptions, operational feasibility, and implementation sequencing Serve as day-to-day bridge between brand and CoE teams , enabling integration and one-voice execution across assigned TA Support...

Serves as the day-to-day bridge between brand teams and the Patient Support CoE for assigned therapeutic areas, owning TA-specific insight generation, patient journey mapping, and implementation support for critical capabilities. Accountable for translating designs and patient-facing capability concepts into operational and scalable solutions — ensuring new capabilities fit into the broader architecture or new capabilities deploy without disrupting live patient support operations. Key Responsibilities Understand and pressure test TA-specific patient support designs , including workflow assumptions, operational feasibility, and implementation sequencing Serve as day-to-day bridge between brand and CoE teams , enabling integration and one-voice execution across assigned TA Support...

Senior Scientist, Biostatistics – Rahway, NJ Serve as statistical representative in the cross-functional teams for the clinical trial planning, execution, and reporting. Develop individual protocols and data analysis plans and determine appropriate statistical methodology for data analysis. Participate in database design meetings to ensure that the data evaluated are in high quality and satisfy analysis requirements. Collaborate with the statistical programming staff to ensure that all programs meet analysis requirements, internal standard operating procedures, and external regulatory requirements. Evaluate appropriateness of available software for planned analyses and ascertains needs for potential program development of novel statistical methodology. Analyze data and...

The Senior Specialist, Engineering, will be responsible for support of production of live virus vaccines within bulk vaccine production and/or final formulation and filling operations. This engineer will be a member of the Technical Operations Deviation Management team in the Live Virus Vaccine Manufacturing End-to-End at the West Point site. The primary responsibility of the individual will be leading investigations associated with manufacturing deviations and development of actions in response to these deviations. Support will be focused on the Deviation Management process including operations support, equipment troubleshooting, implementation of process/ equipment actions, and other related duties. This position will require...

The Research and Development Sciences (RaDS) value team in our company's Research & Development (R&D) Information Technology (IT) brings together product management, engineering, and data science expertise. We enable data, technology, and services that accelerate our scientists’ ability to discover and develop innovative medicines that change the course of human health. In the RaDS value team, the Product organization is responsible for implementing capabilities and associated services to advance the drug discovery and development pipeline. Our IT team operates as a business partner, proposing ideas and innovative solutions that enable new organizational capabilities. We collaborate internationally to deliver the services...

The Associate Director, Global Data Management & Standards (GDMS) Academy reports to the Head of Global Data Management & Standards (GDMS) Business Operations and leads the strategy and execution for GDMS onboarding and the global skill and knowledge development framework. In collaboration with GDMS functional area leaders, translates capability needs into learning pathways, appropriately leveled knowledge content, and role-based curricula. The role defines standards for curriculum design, evaluation, and learning operations, and builds scalable mechanisms for training delivery and consumption. Partnering with enterprise learning and development, leverages curated training and learning sources, ensures alignment on learning technologies, aligns to training...

Global Clinical Trial Operations (GCTO) is a global organization with approximately 10,000 staff operating in 50 countries. The Program and Study Management organization (PSM) is a sub-functional unit within GCTO, divided into therapeutic clusters, and is accountable for operational delivery of the clinical trial portfolio. The Head, PSM is a senior GCTO leadership role responsible for the strategic and operational leadership of a portfolio of clinical programs within assigned Therapeutic Areas (TAs). This role serves as a key and active participant in GCTO Leadership Team (LT) and governance bodies including GCTO Steering Committee, GCTO Sourcing Governance Committee, GCTO Operations Review,...

Position Description The Human Health Finance Center of Excellence (CoE) is responsible for leading the financial planning, analysis, and reporting activities for the Human Health (commercial) division. The Associate Director, Human Health Finance CoE position plays a key role as part of the Human Health CoE and the boarder Finance team. As a member of the COE team, this role is responsible for providing critical financial support for the Human Health Division to make informed business decisions and to help ensure accurate and thorough financial planning and reporting deliverables. Successful performance within this function requires strong analytical and communication skills,...

The Associate Vice President (AVP), Drug Product Technical Operations (DP Tech Ops) provides enterprise technical leadership for drug product manufacturing across the company's commercial manufacturing network, including oversight of external manufacturing partners, technical operations leadership for the Singapore manufacturing facility, and strategic stewardship of in-line product manufacturing across the global network. Reporting to the Vice President, Small Molecule Science & Technology (SM S&T) within the our company's Manufacturing Division, this leader is accountable for ensuring robust, reliable, compliant supply, and continuously improving drug product operations that enable uninterrupted patient supply and support the long-term success of the portfolio. The role...

We are seeking a Growth and Improvement minded Regional Medical Scientific Director (aka Medical Science Liaison, MSL) in Respiratory - COPD that can help drive our Strategic Operating Priorities. Summary, Focus and Purpose The Regional Medical Scientific Director (Medical Science Liaison) is a credentialed (i.e., PhD, PharmD, DNP, MD) Director Level Medical Affairs position and therapeutic and disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs). The role provides balanced, factual, scientific information about non-product areas of interest to the Company and replies to scientific questions from SLs, including questions about Company products....

For over 130 years, we have pioneered groundbreaking science. Today, we are driven by continuous innovation to develop breakthrough medicines, vaccines and technology. Rooted in direct experience on the farm and in the clinic, we work hand in hand with our customers every step of the way. Our singular focus is to empower those who care for animals, helping them manage their vital responsibility with confidence. Because when it comes to animal health, no one sees it like we do. Our Senior Territory Representatives interact face to face with our customers, understand their needs and consult to offer the right...

The Global Pharma pipeline holds significant promise across areas of high unmet medical need, particularly in cardiometabolic disease, with multiple assets advancing into Phase II and III. With late-stage development programs and anticipated launches, Global Pharma is well positioned to drive future growth and meaningful patient impact. Within Global Pharma team, it’s an exciting time as we build an industry-leading cardiometabolic & Neuroscience business that aspires to impact these devastating diseases on a global scale. Our company has made significant progress with advancing our cardiometabolic and rare disease pipeline this year. Moreover, we expect 8 approvals in the next five...

The Sr. Specialist, Sales Force Effectiveness is a hands-on, execution-focused role responsible for field launch readiness, improving customer engagement, and facilitating field execution. In this role, you will translate customer insights into targeted territory actions and call plans; champion adoption of field productivity tools and resources; maintain KPIs and scorecards; and collaborate closely with the Associate Director, Specialty Sales Force Effectiveness, as well as Sales, Marketing, Operations, and Digital Human Health, to design and execute sales force effectiveness initiatives that drive measurable actions and outcomes. Territory & call planning Collaborate with Sales leadership to operationalize call plans and target guidance...

Associate Director, Global Marketing Engagement, DHH Our Digital Human Health (DHH) team is innovating how we understand our patients and their needs. Working cross functionally we are inventing new ways of engaging, interacting with our customers and patients leveraging digital, data and analytics and measuring the impact. The Associate Director, Global Marketing Engagement (GME), DHH will be responsible for developing and delivering data and analytics, generating strategic insights, and addressing US new productglobal marketing teams’ business questions to inform pharma pipeline investments, a successful go-to-market strategy, launch planning activities, and portfolio-level commercial assessments. y and creating synergies with the book...

Our Company is currently seeking an exceptional chemist to join the Discovery Process Chemistry group located at our South San Francisco, CA site. This role offers the opportunity to join a vibrant group of innovative laboratory scientists with broad impacts across our late discovery and early development portfolios. Core responsibilities include the development of innovative solutions to complex chemistry problems across a different portfolio of projects in the discovery phase, from lead identification through candidate selection. A successful candidate is expected to apply cutting edge methodologies to synthetic route design in order to enable medicinal chemistry research and accelerate the...

The Associate Vice President, Therapeutic Area Head (TAH) is a senior physician leader responsible for the strategic oversight of clinical safety assessment and risk management for a broad portfolio of investigational and marketed products across one or more therapeutic areas. Reporting to the Vice President, Clinical Safety and Risk Management (CSRM), this role provides leadership and oversight for teams of Safety Physicians who are accountable for all aspects of safety surveillance, benefit-risk evaluation, signal management, and risk mitigation throughout the product lifecycle. The role also provides strategic direction and partnership to Medical Associates operating within a matrix environment to support...

Position Overview Reporting to the Associate Director of PTO Engineering, the Specialist, Technical Operations Engineer provides technical support for the packaging and medical device assembly lines at the our Manufacturing Division Wilson site. This role is responsible for equipment performance through providing on-site support and troubleshooting of packaging and device assembly operations. The Specialist works closely with Wilson and above-site departments to support the transfer of new products and processes from our Research & Development Division or other of our Manufacturing Division sites to the Wilson site. In addition, the role collaborates with site and global Packaging Technology as well...

Senior Specialist, Global Marketing Engagement (GME), DHH Our Digital Human Health (DHH) team is innovating how we understand our patients and their needs. Working cross functionally we are inventing new ways of engaging, interacting with our customers and patients leveraging digital, data and analytics and measuring the impact. The Senior Specialist, GME, DHH will be responsible for developing and delivering data and analytics, generating strategic insights, and addressing global brand lead and US new product team’s business questions to inform pharma pipeline investments and “beyond” G7 investments. Furthermore, the team member will partner closely with global marketing, regional marketing, clinical...

Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety First, Quality Always, Inclusion for All” mindset striving for continuous improvement. We work in the local plant connected to our global manufacturing network to ensure the highest quality of raw materials, intermediates and finished products. Position We are seeking an Associate Director, Operations for a capital project start-up in Durham, North Carolina. The Associate Director will oversee a portion of the manufacturing team. The facility includes end-to-end processing of drug substance, drug product, including culture growth, harvest, filling, lyophilization,...

Our company's Manufacturing Division, is a team of dedicated, energetic individuals who are committed to being the most trusted supplier of pharmaceuticals and health products worldwide. Our facilities, along with our external contractors, suppliers, and partners, comprise an interdependent global manufacturing network that’s committed to delivering a compliant, reliable supply to customers and patients on time, every time, across the globe. The Senior Maintenance Technician is responsible for providing equipment troubleshooting and maintenance support to Operations areas (sterile supply, weigh/dispense, media, stabilizer/prep, thaw/pool, filling, capping/inspection, clean utilities etc.) located in aseptic and clean room environments. Works within a team to...

Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity, knowledge, imagination, skill, and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your...

Primary Responsibilities Providing a leadership and technical supportive role in the areas of Steam Sterilization, Dry Heat Depyrogenation, Steam Decontamination, Vaporized Hydrogen Peroxide Decontamination, Controlled Temperature Unit Temperature Mapping and Warehouse Temperature Mapping Performance Qualification Validation activities (but not limited to); Scheduling and executing PQ Validation activities Scheduling and managing PQ protocol close-outs Performing technical investigations and analyses Driving to and recommending corrective actions and seeing them through to successful/sustainable implementation Reviewing procedural revisions to be compliant with regulatory expectations Data analysis and Second Person Review Troubleshooting activities associated with all aspects of PQ execution Final report and procedure writing...

The Specialist, Engineering, will be responsible for support of production of live virus vaccines within bulk vaccine production and/or final formulation and filling operations. This engineer will be a member of the Technical Operations Deviation Management team in the Live Virus Vaccine Manufacturing End-to-End at the West Point site. The primary responsibility of the individual will be leading investigations associated with manufacturing deviations and development of actions in response to these deviations. Support will be focused on the Deviation Management process including operations support, equipment troubleshooting, implementation of process/ equipment actions, and other related duties. This position will require development...

For over 130 years, we have pioneered groundbreaking science. Today, we are driven by continuous innovation to develop breakthrough medicines, vaccines and technology. Rooted in direct experience on the farm and in the clinic, we work hand in hand with our customers every step of the way. Our singular focus is to empower those who care for animals, helping them manage their vital responsibility with confidence. Because when it comes to animal health, no one sees it like we do. Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety...

At our company, we are inspired by the belief that a research-driven enterprise dedicated to scientific excellence can create medicines that save and improve lives. Every employee is building on our proud legacy of scientific breakthrough. Our ability to impact the lives of patients worldwide depends on the integrity, creativity, humility and scientific acumen of our team. We are creating a different organization that is inspired by invention and founded on a culture of respect and collaboration. At our company Research Labs (our Research & Development Division) Boston, you’ll have the opportunity to expand your knowledge and skills through collaboration...

CANDIDATE MUST RESIDE IN ONE OF THE FOLLOWING LOCATIONS AND BE FLUENT IN SPANISH South Florida - Ft. Lauderdale, Miami, Boca Raton, Key Largo The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our company policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites. Actively develops and expands...

The HVAC&R Technician is responsible for providing equipment troubleshooting and maintenance support for ongoing facility facility/manufacturing operation and support growth initiatives at the site. Assists in and develops standard operating procedures (SOP's) and preventative maintenance (PM's) plans. Responsible for written documentation of activities. Responsible for SAP transactions and change control activities including spare part lists and Preventative Maintenance (PMs) plans. Actively supports, participates and embraces an inclusive team culture including significant interaction with Operations, Quality, Automation, Technology, and other groups as required. The HVAC&R Technician will provide maintenance supporting vaccine process equipment operations. Takes appropriate action to correct Plant Engineering...

For over 130 years, we have pioneered groundbreaking science. Today, we are driven by continuous innovation to develop breakthrough medicines, vaccines and technology. Rooted in direct experience on the farm and in the clinic, we work hand in hand with our customers every step of the way. Our singular focus is to empower those who care for animals, helping them manage their vital responsibility with confidence. Because when it comes to animal health, no one sees it like we do. The Associate Specialist, Engineering (Biotechnology Solutions) provides technical support for vaccine and biologics process development and manufacturing within a multidisciplinary...

Pharmaceutical Analysis and Digital Technologies (PADT) is seeking an exceptional scientific and operational leader for the role of Senior Director, Stability Operations and Device Program Management. This position will provide strategic ownership and end-to-end leadership for stability operations across the development portfolio through commercialization, while also leading device program management activities that enable integrated delivery of drug-device combination products and associated analytical, technical, and regulatory deliverables. The successful candidate will lead a team of scientists, operational experts, and program management professionals responsible for building and executing a robust, compliant, and scalable stability operations model. The role will require strong people...

An amazing opportunity has arisen for a Digital Manufacturing Operations Director. This is a crucial role that is a trusted partner who fosters enablement of purposeful innovation and sustained value from our digital assets, while enabling a safe, compliant, reliable, and cost-effective supply to our patients. This role provides support to our manufacturing division as they aspire to simultaneously run the business, grow the business, and transform the business. A focus on creating and fostering an engaged and inclusive culture is essential to deliver sustained performance excellence. Responsibilities Direct the technical activities of the shopfloor automation teams responsible for all...

Position Overview - Basic Functions & Responsibility Essential function{s) includes, but is not limited to Reporting to the Associate Director of PTO Engineering, the Senior Specialist Engineer is responsible for providing technical support of our Manufacturing Division-Wilson packaging (including bottle/blister/oral solid dose filling and packaging lines) and medical device (autoinjector assembly and packaging/combination kit packaging) lines. Responsible for technical input on purchasing, installing, and qualifying new packaging and device assembly equipment. Also responsible for packaging and device assembly equipment performance, support, and troubleshooting for products packaged at our Manufacturing Division-Wilson. Works closely with Wilson and above-site departments for the technology...

The South San Francisco DMPK organization is seeking an accomplished and highly collaborative Senior Principal Scientist to provide scientific leadership across drug conjugate discovery and development programs, support strategic portfolio decisions, and advance DMPK capabilities for emerging modalities. This individual will partner closely with discovery biology, translational sciences, clinical development, bioanalytical, toxicology, chemistry, and program teams to enable data-driven decision making from early discovery through clinical candidate nomination and FIH execution. The successful candidate will provide scientific leadership for conjugate DMPK strategy, oversee LM ADME experimentation strategy and capabilities, contribute to portfolio management and prioritization, serve as a program representative...

The Associate Specialist, Engineering, will be responsible for support of production of live virus vaccines within bulk vaccine production and/or final formulation and filling operations. This engineer will be a member of the Technical Operations Deviation Management team in the Live Virus Vaccine Manufacturing End-to-End at the West Point site. The primary responsibility of the individual will be leading investigations associated with manufacturing deviations and development of actions in response to these deviations. Support will be focused on the Deviation Management process including operations support, equipment troubleshooting, implementation of process/ equipment actions, and other related duties. This position will require...

Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines, consumer health products, and animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us. Join our Manufacturing facility in Elkton, Virginia, and be part of a team that values integrity, knowledge, imagination, skill, diversity, and teamwork. As a Senior Manufacturing Automation Engineer, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. The successful candidate will have the...

Role Summary The Director, Strategy Realization serves as a strategic advisor to the MAH IT Leadership Team, responsible for ensuring that organizational strategy is clearly understood, consistently communicated and updated, and effectively translated into enterprise-wide alignment. This leader helps create a shared understanding of MAH IT priorities, transformation efforts, status, and business value across employees, business partners, and enterprise stakeholders. The role combines strategic thinking, organizational alignment, change leadership, stakeholder influence, and strategic impact translation to help aligning priorities, organizational topics and improve understanding of MAH IT's contribution to business outcomes. This position is not responsible for product strategy, portfolio...

We have an exciting opportunity for a physician-scientist to join our group as a Principal Scientist (Clinical Director) in Translational Medicine/Early Clinical Development in the Respiratory Therapeutic Area based in the US (Boston, MA). Translational Medicine at our Research Division is responsible for early clinical development of novel therapeutics, working in close collaboration with our discovery scientists and late-stage clinical researchers. The Respiratory Therapeutic Area specifically focuses on development in the respiratory system, including diseases of the airways, parenchyma, and pulmonary vasculature. We are seeking a highly qualified individual for a position in our group. The ideal candidate for this...

Are you looking for an exciting opportunity with a rapidly growing pharmaceutical manufacturer? If so, then this is the opportunity for you! Manufacturing Division, is a team of dedicated, energetic individuals who are committed to being the most trusted supplier of pharmaceuticals and health products worldwide. Our facilities, along with our external contractors, suppliers, and partners, comprise an interdependent global manufacturing network that’s committed to delivering a compliant, reliable supply to customers and patients on time, every time, across the globe. The Senior Maintenance Technician is responsible for providing equipment troubleshooting and maintenance support to VMF Operations areas (sterile supply,...

The Technician (Technical), Operations role is an excellent opportunity for individuals with experience in manufacturing and/or packaging operations who are proficient with basic mechanical/electrical equipment troubleshooting, maintenance, and repair. This role will serve as the first responder to challenges that arise with manufacturing and packaging equipment, effectively diagnosing and addressing technical issues. Key responsibilities include following manufacturing and packaging requirements, adhering to Good Manufacturing Practices (GMP), and completing daily tasks according to established procedures under the Operations Manager's guidance while collaborating with team members to ensure safe and timely production of high-quality products. The Technician (Technical) position will operate equipment,...

For over 130 years, we have pioneered groundbreaking science. Today, we are driven by continuous innovation to develop breakthrough medicines, vaccines and technology. Rooted in direct experience on the farm and in the clinic, we work hand in hand with our customers every step of the way. Our singular focus is to empower those who care for animals, helping them manage their vital responsibility with confidence. Because when it comes to animal health, no one sees it like we do. The Operations Technician position is available at our Company's Animal Health facility in Worthington, Minnesota. The Worthington facility is expanding...