Merck Job Trends

This role provides strategic leadership and scientific oversight to part of the cardiometabolic (CMD) therapeutic area (TA) portfolio in the department of Quantitative Pharmacology and Pharmacometrics (QP2). The Team Leader (Senior Director) is responsible for application of cutting-edge quantitative pharmacology and pharmacometrics strategies to propel the internal portfolio forward leveraging the full strength of the QP2 department. The CMD TA Team Leader will be tasked with overseeing a team of QP2 scientists, providing guidance in personnel management, scientific strategy, and operational execution, in addition to serving as QP2 lead on assigned projects. Reporting directly to the QP2 CMD Head and...

This position is in our organization’s Device Development & Technology (DD&T) group in our Research division. Our organization’s DD&T group is responsible for the development of devices, combination products, processes, testing and assembly equipment from conception through product launch. Products include autoinjectors, inhalers, implants, infusion pumps, vaginal rings and connected devices/apps. The person in this position contributes to high impact, complex, cross-functional, and cross-divisional teams, initiatives and will provide input to achieve project goals. Effective collaboration with teams is essential to meet our company's goals/objectives. The group also plays a key role in supporting commercially launched products. Our company's DD&T...

Our Digital Manufacturing Operations organization supporting the dynamic West Point site is seeking a Senior Specialist in Process Automation to join the team. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and collaboration of individuals. To this end, we strive to create an environment of mutual respect, encouragement, and teamwork. As part of our team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. This role will lead a team of engineers in providing automation system support and expertise to enable our manufacturing division in the reliable...

We are seeking a highly skilled and strategic Reliability Engineering Director to lead our reliability engineering efforts within the Vaccine manufacturing environment. This role is critical to ensuring the continuous, compliant, and efficient operation of manufacturing equipment and systems that support drug production. The ideal candidate will combine deep technical expertise in reliability engineering with strong leadership capabilities and a thorough understanding of pharmaceutical industry regulations and quality standards. Key Responsibilities Lead and develop the reliability engineering team composed of engineers focused on vaccine manufacturing equipment and systems. Develop and implement reliability strategies to maximize equipment uptime, reduce unplanned downtime,...

The Hospital / Institutional Customer Representative is a key member of the Hospital Customer Team and plays a critical role in supporting our Company's customer centric business model. He/she is responsible for working with the Hospital Customer Team to understand and identify Health Care Provider (HCP) customer needs, support pull-through activities relative to the customer strategy, and ensure that our Company is viewed as demonstrating value and better health outcomes to healthcare professionals and their patients. Territory Information Territory covers Sacramento, Roseville, Walnut Creek, Stockton and Yuba City, CA. The selected Sales Representative must reside within the territory. Overnight travel...

As a Chronic Care Specialty Sales Representative, 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 specific territory. Travel (%) depends on the needs of the territory and where the selected candidate resides, and overnight travel may be required about 25% of the time to...

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 to 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 may include but are not limited to Direct the technical...

The Director, Business Insights Analytics is responsible for developing and communicating data-driven and actionable insights that drive greater customer and market understanding to inform launch & go-to market strategies and help meet in-line commercial objectives. The individual in this role will be an independent contributor as well as lead a team and, together, will act as the Commercial Insight & Analytics Lead for US marketing teams. The ideal candidate will lead an insight team consisting of functional teams across market research, data strategy, forecasting, commercial effectiveness, measurement, marketing/sales operations, digital analytics, competitive insights and strategy. This person will help scope,...

The Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our Company's Oncology medicines span all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Senior Director may be responsible for Evaluating pre-clinical and translational work for the purpose of generating early clinical development plans and Investigational New Drug applications Development of clinical development strategies for investigational or marketed Oncology drugs Planning clinical trials (design,...

Director – Discovery Oncology Discovery Oncology is seeking a visionary and driven people leader to discover and advance the next Oncology therapeutics. Come join an incredible team steeped in a history of scientific excellence and successful drug discovery. The successful candidate will lead a team at our company's Boston site focused on immune engaging biologics as well as additional modalities. They will partner across to help build our Discovery Oncology strategy and our expanding pipeline. This leader will work tightly with clinical, translational, and business development colleagues to ensure an effective pipeline of compelling medicines. The successful candidate will have...

Within our GPO External Manufacturing organization, the Integrated Launch Excellence Platform is responsible for converting our pipeline to products through commercialization activities at CMOs for Drug Substance and Drug Products. Additionally, the Platform has responsibility for accelerating our regionalization strategies and in ensuring CMOs manufacturing our acquired assets are integrated into our external network. The scope of activity, along with the partner groups, encompasses strategic sourcing and technical transfer phased from pre-PPQ through post launch builds for sustained, reliable compliant supply at a competitive cost. The Director of Operations will interact with key operational and functional leaders and will be...

The Animal Technician II, under the guidance of a Vivarium manager, works to support innovative translational models to impact drug safety assessment, development and discovery and improve human health. Under the direction of a manager or assigned technical staff within Laboratory Animal Resources, Nonclinical Drug Safety, and Veterinary Products the Animal/Laboratory Technician performs animal care related functions. Other duties include routine maintenance, animal handling and restraint, and assumes full responsibility and accountability for performance and documentation of all assigned functions for all the various animal species housed in accordance with the Animal Welfare Act, AAALAC- International, our company's Worldwide policy...

The Rahway FLEx (Formulation Laboratory & Experimentation) Center is a flexible, agile facility that brings together capabilities, operations, and talent to accelerate the pipeline— Pharmaceutical Operations & Clinical Supply is seeking applicants for a Manufacturing Engineering Lead to support specialty dosage forms and oral solid dosage (OSD) GMP development activities on second shift. The successful incumbent will serve as the technical lead for shift production, coordinating safety, quality, and equipment decisions. This role evaluates safety, product/process quality, and equipment performance and determines the appropriate path forward to protect patients, people, and compliance. Key Responsibilities Own technical decisions for the shift...

We are seeking a highly motivated and experienced Director for New Products Marketing within US Oncology. The scope of responsibility for the New Products team includes both oncology and hematology assets in development. This Director role will report directly to the Executive Director who leads this New Products team. As a Director for New Products, you will lead commercial strategy for selected pipeline assets from early development through handoff to launch teams, partnering closely with our global marketing partners, as well as teams in the US market who focus on in‑line marketing, organized customer access and reimbursement, medical affairs and...

Our market access team is passionate about bringing our medicines and vaccines to our customers around the world. We strive to understand our customers’ needs and provide solutions to meet their needs. The Director, Global Oncology Market Access Lung will have GMAx responsibilities for the developmenent of the access strategies for the pipeline assets with Lung indications. The candidate will be expected to have deep knowledge of the Lung cancer access landscape to ensure market access considerations are embedded early in the development of assets respective to their lung indications. As a GMAx lead, the candidate would need to synthesize...

The selected candidate will work in the Pharmaceutical Analysis & Digital Technologies (PADT) department within the Development Sciences and Clinical Supplies (DSCS) organization and serve as a primary point of contact for externalized analytical deliverables supporting Biologic development programs at various stages of development. The scope of the role will include realization of the analytical R&D externalization strategy by building analytical capabilities and driving a culture of scientific and operational excellence at our external partners including oversight of a rapidly growing team of external analysts. The candidate will partner with cross functional Development and Commercialization Teams (DCT’s) and external partners...

The Associate Director, Oncology Market Access Insights will lead analytical strategy and execution to assess payer landscapes, optimize access, and inform pricing and contracting decisions. This role will support the end-to-end analytics lifecycle—from data ingestion and engineering to advanced analytics and visualization—leveraging secondary data sources (especially medical and pharmacy claims data, formulary data, and payer policy data). The ideal candidate combines strong technical skills in SQL, Python, and Power BI with deep domain expertise in U.S. market access, payer dynamics, and buy-and-bill vs. pharmacy distribution models. Key Responsibilities Define and execute the analytics roadmap to support Oncology market access objectives...

This position sits within National Contract Ops & Supply Chain (NCOSC), which delivers best-in-class, end-to-end services aimed at providing affordable patient access, insightful customer experiences, and enriching employee experiences for IAM Contract Management, Service Agreements, Account Management, and Channel Strategy lifecycles. The Integrated Account Management (IAM) Team manages direct account and contract responsibility across the entire US health care system for our Company's commercial and government business. The Customer Manager (CM) acts as a unique and critical connection point in this dynamic environment to bridge field and internal stakeholders for the purpose of reaching mutually beneficial customer contracts. In close...

The Senior Specialist Digital and Data Quality will be responsible for the quality aspects of GMP computerized systems and the supporting infrastructure used in site facilities, utilities, manufacturing, packaging, labeling, and laboratories to ensure compliance with company policies, procedures and regulatory expectations. This includes involvement in all quality-related activities for computerized systems which are required by our Manufacturing Division Quality Manual or with potential for impact on product quality, patient safety or data integrity. The position will work closely with stakeholders and SME’s from site operations, quality operations, IT, automation and engineering to provide evidence of quality oversight throughout the...

The Future Talent Program features Cooperative (Co-op) education that lasts up to 6 months and will include one or more projects. These opportunities in our Manufacturing & Supply Division can provide you with great development and a chance to see if we are the right company for your long-term goals. The co-op assignment will support our Manufacturing Division’s Packaging Technology Community’s three unique groups. These groups serve as our company’s central packaging Centers of Excellence with global responsibility for packaging related activities. The position is based in West Point, PA (a suburb of Philadelphia). The candidate selected will have opportunities...

Associate Director, Raw Material & Release Management Within Planning and Manufacturing Systems (PAMS) in our Research Division's Bioprocess Clinical Manufacturing and Technology (BCMT), the Associate Director, Raw Material & Release Management (P4) is the single accountable lead for end-to-end management of raw materials, culture media/buffers, excipients, single-use components, and GMP supplies that support pilot-scale GMP manufacture of clinical biologic bulk (vaccines, therapeutic proteins, monoclonal antibodies). Based in the Biologics Pilot Plant (BPP) / VAX PR&D environment, this role combines advanced materials planning and procurement with release management, validated system stewardship, and cross‑functional leadership to ensure compliant, timely, and cost‑effective material...

We’re seeking an experienced candidate to join our Operations Orchestration team in an Associate Director level role, supporting digital transformation across our global manufacturing shop floors. Reporting to the Operations Orchestration Product Manager, this role provides senior execution and technical leadership for industrial data platforms, helping translate product direction into scalable, reliable solutions delivered through a global team model. Pharmaceutical manufacturing experience is strongly preferred. In this role, you will act as a senior execution leader and technical authority, working closely with manufacturing, automation, and IT stakeholders across regions while partnering with established delivery and support teams worldwide. Why this...

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. This position supports statistical programming activities for multiple late-stage drug/vaccine clinical development projects. Accountability predominantly includes 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...

The Materials and Biophysical Characterization group in Analytical Research and Development is seeking a highly self-motivated and innovative scientist with deep knowledge and problem-solving skills in biotherapeutics characterization. The Materials and Biophysical Characterization team is responsible for building the mechanistic understanding of the interplay between formulation composition, stability, device, and process to ensure robustness and quality of drug substances and drug products in the biotherapeutics pipeline. As a Senior Scientist, you will be contributing to projects in a diverse biotherapeutics pipeline by developing and implementing biophysical and particle characterization assays and collaborating with process, formulation and device functions as part...

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. This role will primarily support Manufacturing Operations and will serve as the Quality Integrated Process Team (IPT) Representative for the...

We are seeking a highly motivated and experienced Director for New Products Marketing within US Oncology. The scope of responsibility for the New Products team includes both oncology and hematology assets in development. This Director role will report directly to the Executive Director who leads this New Products team. As a Director for New Products, you will lead commercial strategy for selected pipeline assets from early development through handoff to launch teams, partnering closely with our global marketing partners, as well as teams in the US market who focus on in‑line marketing, organized customer access and reimbursement, medical affairs and...

The Director of Customer Care is a key position in our company transforming our Customer Care organization. This role is responsible for elevating customer experience by evaluating and evolving our customer care model, which has been scaled alongside business growth and acquisitions. The incumbent will ensure internal and external customer journeys are seamless—enabled through a single point of entry and a customer-centric team delivering personalized, high-value interactions aligned to customer attributes. This leader will ensure that people, processes, systems, and third-party resources are harmonized and simplified to deliver end-to-end transparency, aligned KPIs, and consistently high customer satisfaction. In parallel, the...

Director, Global Marketing Engagement, Early Assets, 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 measuring the impact. The Director, Global Marketing Engagement (GME), DHH will be responsible to lead delivery of data and analytics, generating strategic integrated insights, and proactively influence global brand leads and US new product team’s business questions to inform pharma pipeline investments and launch readiness. Furthermore, the leader will partner closely with global marketing, regional marketing,...

The Learning Consultant supports Learning Directors and Learning Partners in the execution of the L&D strategy through consulting and delivery on appropriate learning solutions. S/he applies understanding of key business priorities/processes and internal and external best practices to learning solutions. Partners with key divisional stakeholders to identify performance needs and gaps, collaborates with design experts and operational support points on desired performance and business outcomes. Builds and maintains strong business relationships and learn from and apply insights from an integrated learning network. Success in this role depends on a candidate’s ability to apply adult learning theory in his/her area of...

The Vaccine Analytical Research & Development department is seeking applicants for a Senior Scientist position available at its West Point, Pennsylvania, research facility. The Senior Scientist is a laboratory-based scientific role that establishes and maintains laboratory automation and robotic systems used to support high-throughput analytical assays. The successful candidate will be tasked with solving complex analytical problems at the interface of biology, chemistry, and lab informatics to enable vaccine development, support process and formulation development, conduct vaccine investigations, and manage the method lifecycle. In this role, the individual will maintain and implement analytical methods on robotic platforms to support high-throughput...

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...

Lead Associate, Administrative Services Global Oncology Marketing Global Oncology 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 members of the Global Oncology leadership team, the Lead Associate, Administrative Services will provide administrative support to the assigned leaders within the Global Oncology organization. The primary activities include and are not limited to the following Coordinates and performs multiple administrative tasks, including calendar scheduling, meeting management, travel and expense management Completes various work assignments requiring...

The Senior Specialist, Scientific Nomenclature & Reference Data is an individual contributor who supports the stewardship, curation, and integration of chemical, biologic and vaccine product reference data across the drug development lifecycle. This role blends deep chemistry domain expertise, hands-on nomenclature skills, and practical master data capabilities to deliver accurate, traceable, and usable reference data for scientific, regulatory, and other business stakeholders. The Senior Specialist will continuously improve data quality, governance, and automation approaches, so the capability remains adaptable as technologies and ways of working evolve. Primary activities include, but are not limited to Derive and assign correct nomenclature (IUPAC...

Directors in Quantitative Pharmacology and Pharmacometrics (QP2) apply quantitative approaches to characterize clinical pharmacokinetics and pharmacodynamics of new chemical entities and biologics , inform dose selection and go/no-go decisions, and shape, present and defend regulatory strategies to support global regulatory submissions and post-approval expansions in indications . Directors perform job duties independently with minimal supervision, lead QP2 efforts on drug development programs, and author strategic documents. Directors are expected to have or be developing expertise in several areas, including Serving as an expert representative for QP2 on teams developing infectious disease or vaccine assets Framing critical drug development questions for...

The Screening & Compound Profiling group at our Research Laboratories site in Rahway, NJ, is seeking a highly motivated Automation Scientist to join our Automation & Informatics team in the Screening and Compound Profiling group. The successful candidate will be responsible for operating automated systems to execute various biochemical and cell-based assays accurately and efficiently, ensuring the integrity and traceability of the data generated. They will also participate in maintaining and optimizing automated systems and processes to enhance capabilities for target and lead discovery across diverse therapeutic areas, including oncology, immunology, neuroscience, cardiometabolic, and infectious disease. The individual will work...

Wil jij impact maken in de biotechsector? Wij produceren hoogwaardige vaccins die het welzijn van dieren verbeteren en wereldwijd bijdragen aan voedselveiligheid. Werk met moderne technologie in een veilige, stimulerende omgeving waar samenwerking centraal staat. Sluit je aan bij ons team in De Bilt als 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...

Description Générale Pour notre site de Beaucouzé (49), proche Angers, nous recherchons un(e) Responsable Grands Comptes Porcs (H/F) qui a pour mission principale de représenter la société et d’assurer les ventes et le suivi de clients considérés comme des Grands Comptes (centrale de référencement, groupement ou cabinet de vétérinaires partenaire d’une centrale de référencement…). Activités principales Zone de responsabilité Grand Ouest de la France Participer à l’élaboration des solutions clients, et à la mise en place d’offres destinées à répondre à leurs attentes et besoins Définir et mettre en œuvre les plans d'actions nécessaires à l'atteinte des...

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 Quality Assurance group ensures every single material inside our products is manufactured, processed, tested, packaged, stored and distributed aligned...

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 contribute to our mission of using the power of leading-edge science to save and improve lives around the world. The Director, Operations, serves as the business unit leader for the Bottles & Blisters Integrated Process Team (IPT), overseeing primary and secondary packaging operations that support a wide range of company products. This role is accountable for the overall performance of the IPT and acts...

The Future Talent Program features Cooperative (Co-op) education that lasts 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. Global Engineering Solutions (GES) is responsible for the design, construction, and delivery of advanced manufacturing facilities and laboratories worldwide. We provide premier engineering solutions in the pharmaceutical industry through technical innovation and project management to deliver important life-saving medicines and vaccines to patients. With our extensive range of facilities and environments, our...

Our Research Scientists are our Inventors. We identify and target steps in disease mechanisms or pathways that could be inhibited or enhanced. Our goal is to isolate a compound that is effective against a disease target. Using innovative thinking, state-of-the-art facilities, and robust scientific methodology, we collaborate to discover the next medical breakthrough. Seeking candidates for a Specialist position within our company’s research laboratories Biologics Pilot Plant (BPP) Process Engineering Tech Transfer Team. This person will work on the preparation, and support execution, of pilot-scale campaigns for the Good Manufacturing Practice (GMP) manufacture of bulk vaccine and biologics clinical drug...

The Senior Director (Sr. Principal Scientist) has primary responsibility for the strategic planning and directing clinical research activities involving investigational compounds in Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire cycle of clinical development, including determination of appropriate disease indications to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. Specifically, The Senior Director May Be Responsible For Evaluating pre-clinical and translational work for the purpose of generating the early clinical development plan and Investigational New Drug applications. Providing clinical development support of business development assessments of external opportunities...

Global Marketing, Director – Hematology Assets We are currently recruiting for a Director Global Oncology Marketing – Hematology Team. The Director of Global Oncology Marketing – Hematology Assets will collaborate closely with the Disease Asset Leads to develop and execute the Commercial strategy of late-stage hematology assets. This position will require outstanding leadership in launch preparation and will report to the Executive Director, Global Oncology/Hematology Marketing - Leukemia. Key responsibilities include, but are not limited to collaborating with Heme Asset and Disease Leads to the following Provide commercial leadership in close collaboration with Late-Stage Heme Asset Leads Drive innovative global...

Location West Point, PA or Rahway, NJ Digital is the multiplier that will allow Development Sciences and Clinical Supply (DSCS) to deliver better experiments faster, efficient filing and launch, more robust supply chains and higher-confidence decisions across the portfolio. The DSCS Digital Technologies organization is responsible for the invention and application of new data-rich tools to support scientists across process development, drug product development and analytical development within DSCS at our Company. We aspire to embed data-intense technologies into the fabric of DSCS culture. The tools that we develop are as diverse as the team developing them, and in this...

Join our dynamic team at the forefront of transforming the US market through innovative product launches and launch excellence within our US Market Strategy organization. We are dedicated to improving lives through human-centered healthcare solutions, and we seek individuals who are passionate about driving impactful changes. As the Associate Director of Launch Strategy and Operations, you will lead the enterprise preparation of multiple product launches in Oncology. You will collaborate closely with marketing leadership, as well as partner with cross-functional teams to develop and implement strategic launch plans, ensuring market readiness and optimizing commercial success. This role requires a blend...

Associate Director, Campaign Development Lead (CDL) Commercial Excellence & Innovation US Oncology Business Unit This individual will lead the identification, design, execution, oversight, and optimization of the US Healthcare Professional (HCP) campaigns and programs that support the strategic imperatives for our Oncology products. Primary Responsibilities Responsibilities include, but are not limited to the following Owning the content strategy & campaigns to ensure all tactics achieve desired customer experience Leading the development of content for the field resources (iPad & field emails) Leading the development of content for digital promotional assets, such as emails, display units, banner ads, alerts, web content,...

This individual will lead the development and delivery of integrated marketing communications plans and multi-channel programs, supporting the strategic imperatives for the Oncology Franchise. The Associate Director, Consumer Campaign Development Lead (CDL) will partner with the marketing strategy team to lead patient experience and engagement activities for our Oncology Lung product. The role focuses on designing, executing, and optimizing patient‑centric campaign tactics and digital media to support the brand launch and DTC activities. The CDL will work cross‑functionally with brand and commercial leads, Medical, Legal/Regulatory, Analytics, Agencies, and Operations to develop compliant, measurable tactics that support patient acquisition, access, education,...

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 The candidate will be working with process engineers and formulations in oral solid and liquid dosage forms. The position requires someone who can demonstrate good attention to detail and achieve a consistent error-free execution of daily job responsibilities, be able to complete documentation using Good Documentation Practices and be able to identify opportunities for process improvement and employ basic problem-solving skills . Responsibilities/Duties/skills Work under the guidance of formulator/engineer to operate the...

Our Research Scientists are our Inventors. We identify and target steps in disease mechanisms or pathways that could be inhibited or enhanced. Our goal is to isolate a compound that is effective against a disease target. Using innovative thinking, state-of-the-art facilities, and robust scientific methodology, we collaborate to discover the next medical breakthrough. Seeking candidates for an Associate Specialist position within our company’s research laboratories Biologics Pilot Plant (BPP) Process Engineering Tech Transfer Team. This person will work on the preparation and support execution of pilot-scale campaigns for the Good Manufacturing Practice (GMP) manufacture of bulk vaccine and biologics clinical...

Associate Principal Scientist, Laboratory Automation Engineer in Digital Technologies Lab Automation Location Rahway, NJ Digital is the multiplier that will allow Development Sciences and Clinical Supply (DSCS) to deliver better experiments faster, efficient filing and launch, more robust supply chains and higher-confidence decisions across the portfolio. The DSCS Digital Technologies organization is responsible for the invention and application of new data-rich tools to support scientists across process development, drug product development and analytical development within DSCS at our company. We aspire to embed data-intense technologies into the fabric of DSCS culture. The tools that we develop are as diverse as...

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...

Our Research Scientists are our Inventors. We identify and target steps in disease mechanisms or pathways that could be inhibited or enhanced. Our goal is to isolate a compound that is effective against a disease target. Using innovative thinking, state-of-the-art facilities and robust scientific methodology, we collaborate to discover the next medical breakthrough. Seeking candidates for a Specialist position within our company's research laboratories Biologics Pilot Plant (BPP) Operations Team. This person will work on pilot-scale campaigns for the Good Manufacturing Practice (GMP) manufacture of bulk clinical supplies, leading unit operations on either upstream or downstream steps, and contributing to...

The Executive Director of Metabolism & Obesity will be responsible for overseeing and facilitating the research in metabolic diseases & obesity and its co-morbidities, in the Cardiometabolic Disease (CMD) Discovery Biology Department, which is located at a new state-of-the-art Research Laboratories center in South San Francisco, CA. The individual will contribute to the design, prioritization, and execution of the strategic plan within CMD, including integration of new technology platforms, human biology, data science, while focusing on uncovering novel biology that delivers high-quality drug discovery pipeline. We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that...

We're looking for a FPA Scientific Field and Technology Solutions Sales Affairs to support the Food Production Business Unit. The main roles of the positions are Maximize resources and approach towards One Health challenges; Facing the of Animal Health develop an approach that leverage on the market; Collaborate with Scientific field affairs, guaranteeing the correct product placement; Develop and implement with the commercial team, the strategic plan for Food Production Animals; Contribute to the Customer Omnichannel Engagement plan, in collaboration with Omnichannel Team, including digital engagement, identification of personas, messages/content, channel mix; Developing the business in order to connect the...

The Hospital / Institutional Customer Representative is a key member of the Hospital Customer Team and plays a critical role in supporting our Company's customer centric business model. He/she is responsible for working with the Hospital Customer Team to understand and identify Health Care Provider (HCP) customer needs, support pull-through activities relative to the customer strategy, and ensure that our Company is viewed as demonstrating value and better health outcomes to healthcare professionals and their patients. Territory covers Seattle, WA. The selected Sales Representative must reside within the territory. Overnight travel may be required. Travel (%) varies based on candidate’s...

The Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across our Company's Research Laboratories full portfolio of clinical trials. GCS is accountable for the planning, sourcing, labeling, packaging and delivery of clinical supplies to clinical sites globally. The GCS Planning (Planning) organization is the key interface between clinical development teams and the operational/executional arms within the business. Working independently, the Protocol Clinical Supplies Project Manager (Protocol CSPM) designs strategic and operational plans for all activities associated with clinical supplies for their assigned studies, which could vary in complexity. This individual serves as the...

The Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across our Company's Research Laboratories portfolio of clinical trials. GCS is accountable for the planning, sourcing, labeling, packaging and delivery of clinical supplies to clinical sites globally. The GCS Planning (Planning) organization is the key interface between clinical development teams and the operational/executional arms within the business. Working independently, the Protocol Clinical Supplies Project Manager (Protocol CSPM) designs strategic and operational plans for all activities associated with clinical supplies for their assigned studies, which could vary in complexity. This individual serves as the primary...

US Analytical Technology Solutions (US-ATS) supports all Animal Health sites globally in analytical method development, improvement, validation, transfer as well as in all kinds of analytical investigations. This position will lead and oversee all aspects of analytical life cycle management activities for in-line licensed products and introduce new innovative analytical technologies. The Analytical Technical Solutions (ATS) Site Lead provides strategic, scientific, and operational leadership for analytical development activities across US sites. The role ensures compliant, efficient, and innovative analytical support for biologics, vaccines, and biotherapeutics while enabling cross‑functional alignment, regulatory readiness, and business continuity. This position is in Millsboro, Delaware-US...

O2- Technician, Operations We are seeking a motivated candidate to join our buffer preparation team within the Media and Solution Sciences (MSS) group, as part of the larger Biologics Process Research and Development (BPR&D) organization. The position will provide an opportunity for learning and development in a professional lab setting, contributing to development and commercialization of our company's life-saving biologics therapeutics. The primary responsibility for this position will be the support of the solution preparation team. The ideal candidate should have experience with small scale and/or large-scale bioprocess equipment, including stainless steel and single use mixing tanks, sterile filtration, aseptic...

The Materials and Biophysical Characterization group in Analytical Research and Development is seeking a highly self-motivated and innovative scientist with deep knowledge and problem-solving skills in biotherapeutics characterization. The Materials and Biophysical Characterization team is responsible for building the mechanistic understanding of the interplay between formulation composition, stability, device, and process to ensure robustness and quality of drug substances and drug products in the biotherapeutics pipeline. As a Principal Scientist, you will be leading and/or contributing to projects in a diverse biotherapeutics pipeline by developing and implementing biophysical and particle characterization tools. In addition to your responsibilities as an individual...

Associate Director, Launch Strategy & Operations US Human Health – US Pharma, Rare Disease Business Unit Location North Wales (Upper Gwynedd), PA | Hybrid (3 days on‑site) About the Role We are looking for a high‑potential launch leader to join our US Human Health Specialty Business Unit as an Associate Director, Launch Strategy & Operations . This role sits at the center of how we prepare, align, and execute product launches—working across marketing, access, sales, operations, medical, and enterprise partners to ensure our launches are thoughtful, connected, and built for long‑term success. This is an ideal role for someone who...

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...

Associate Principal Scientist, Biologics Analytical Research & Development Our Research Scientists are our Inventors. Using innovative thinking, state-of-the-art facilities and robust scientific methodology, we collaborate to discover the next medical breakthrough. The Biologics Analytical Research & Development department (BAR&D) is seeking an Associate Principal Scientist position at the Rahway, New Jersey site. This role is a laboratory-based scientific role tasked with solving complex analytical challenges, to enable development of Biologics drug products. The successful candidate must function well in a collaborative, fast-paced, multidisciplinary team environment. The qualified candidate will be responsible for development, qualification, implementation, troubleshooting and transfer of analytical...

As a Chronic Care Specialty Sales Representative, 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 Northwest Arkansas territory including Fayetteville, AR. Travel (%) depends on the needs of the territory and where the selected candidate resides, and overnight travel may be required about 25% of...

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 diverse 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...

Role Description The Center of Efficiency Lead operationalizes platform strategy through standardized configurations, reusable integrations, and optimized data flows, maximizing enterprise reuse and scalability. This role serves as the execution engine of the Veeva Platform Operating Model, focusing on cross-divisional efficiency rather than local optimization. Key Responsibilities Lead platform standardization, integration, and optimization initiatives Collect and rationalize divisional backlogs and feature requests Track record operationalizing platform strategy into reusable patterns and measurable reduction of duplication/rework. Comfortable managing enterprise backlog rationalization conversations and aligning diverse stakeholders on “reuse-first” outcomes. Maintain direct alignment with Veeva SMEs on roadmap and feature activation Define...

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. JOB SUMMARY This position delivers high-quality customer service to both external and internal customers in a hybrid work environment. The...

Associate Principal Statistical Programmer, Submission Data Standards Quality Management In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our 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 The Associate Principal Statistical Programmer, Submission Data Standards Quality Management (SDS QM), provides oversight and quality management of submission data standard deliverables for world-wide regulatory application submissions of drug and vaccine clinical...

At our company, we are dedicated to advancing the prevention and treatment of diseases in people and animals through innovative health solutions. We are seeking a passionate and experienced Associate Director of Engineering to join our team. This role offers a unique opportunity to contribute to the development of cutting-edge biologic and vaccine drug substances, drug products, and medical device combination products. If you are driven by the power of leading-edge science and want to make a meaningful impact on global health, we invite you to apply. Responsibilities Provide technical expertise from initial design concept through product launch with a...

Role Description The Financial Operations Lead translates platform spend into unit economics, ROI, and optimization opportunities. The role ensures disciplined investment governance and sustained value realization across the Veeva Platform. It provides enterprise-level cost transparency, financial governance, and value realization tracking for the Veeva platform. This position operates at the platform and process level, connecting cost, outcomes, and adoption across divisions. Key Responsibilities Establish and manage platform unit economics and TCO baselines Strong communication skills for cross-functional leadership forums; comfortable driving transparency and cadence-based reporting. Lead cost optimization initiatives and optimization sprints Define showback and chargeback frameworks Streamline procurement processes...

Role Description The Veeva Platform Architect is accountable for the overall architectural integrity and strategic alignment of the Veeva platform across divisions. The role ensures that Veeva operates as a cohesive enterprise platform rather than a collection of independent vault implementations, balancing speed, compliance, and scalability. This role operates above individual programs and vaults, owning enterprise-wide architectural coherence and outcomes. It is the single point of accountability for platform-level architectural alignment across the organization. Key Responsibilities Define and maintain enterprise Veeva platform architecture, principles, standards and guardrails and establish Platform principles, standards, and ways of working Demonstrated experience establishing and...

Role Summary The Health Systems Medical Affairs Director (HS MAD) is a therapeutic and disease expert who develops ongoing professional relationships with healthcare decision makers across key payer and provider organizations. The HS MAD provides accurate information across the full product portfolio, clinical science, and quality management in a balanced and credible manner consistent with the regulatory environment and company’s ethical standards. This role also serves as a resource for the Medical Affairs (MA) management team on strategic planning and provides mentoring for other team members. Location This is a remote position that serves the territory of PA, NJ, &...

Our Research Scientists are our Inventors. We identify and target steps in disease mechanisms or pathways that could be inhibited or enhanced. Our goal is to isolate a compound that is effective against a disease target. Using innovative thinking, state-of-the-art facilities, and robust scientific methodology, we collaborate to discover the next medical breakthrough. Seeking a candidate for a leadership position in our Research & Development Division’s Biologics Pilot Plant (BPP) Process Operations Team. We are recruiting a highly motivated and experienced person to lead teams of process engineers in Bioprocess Clinical Manufacturing and Technology. This role will focus on two...

This position will be responsible for leading and implementing medical device and combination product design controls for both new products and inline products from early design concept definition through commercialization to support regulatory filing, product launch, and post-market surveillance. This position will interact with cross-functional development teams within and external to Device Development. The incumbent must be able to work well with all levels of employees and be able to effectively coordinate the execution of device development strategies. This individual will be expected to apply his/her knowledge of product development and design control principles to positively support and influence clinical...

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 Develops, coordinates, and provides biostatistical support for related drug/vaccine projects under supervision in Late Development Statistics. Interacts with Clinical, Regulatory, Statistical Programming, Data Management and other Scientists part of our Research & Development Division in designing and analyzing clinical trials,...

Job Location West Point, PA The Department of Pharmacokinetics, Dynamics, Metabolism, and Bioanalytics (PDMB) is seeking a bioanalytical scientist to join our Regulated PK & ADA Bioanalytical group at West Point, PA. We are looking for a highly motivated candidate with experience in advanced analytical method design through the use of automation and operational support of bioanalytical labs conducting bioanalysis of biotherapeutics in regulated drug development studies. Collaboration, innovation, teamwork, and accountability are highly valued within our team. The successful candidate will play a key role in designing, planning, and utilizing automation methods during method development, validation, and sample analysis...

Are you ready to make a significant impact in the world of biopharmaceuticals purification? At The Associate Principal Scientist (Associate Director) provides technical and scientific leadership to advance late-stage and commercial biologics from development into reliable manufacturing. This role is responsible for designing, scaling, and transferring purification processes that ensure biological drug substances are produced safely, consistently, and in compliance with regulatory requirements. By partnering closely with process development, manufacturing, quality, and regulatory teams, the Associate Principal Scientist helps establish robust control strategies that support product licensure and long-term commercial success. Responsibilities Participate in and/or spearhead cross-divisional technical teams...

of the job 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 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...

We seek a highly motivated and skilled chemist as a Senior Scientist to join our Labeled Compound Synthesis (LCS) group within the Discovery Process Chemistry organization located at our Rahway, NJ site. This role offers the opportunity to join a unique group of innovative laboratory scientists focused on synthesizing isotopically labeled compounds, essential to support drug discovery and development, and developing novel isotope labeling methodologies to enable and speed up and accelerate drug discovery and development. As a Senior Scientist, you will work on collaborative teams to design and synthesize stable and radioactive isotope-labeled drug candidates and metabolites using modern...

The Vaccines & Advanced Biotechnologies department, part of our company Research Labs, is looking for a passionate and talented systems biologist with expertise in the generation and analysis of complex multi-dimensional and multi-scale biological data to join our research team and support our company discovery & development efforts at West Point, PA. In this role, you will be at the very leading-edge of therapeutic research and development, developing and implementing experimental and computational tools in a dynamic and scientifically rigorous environment. You will operate in a highly collaborative and matrixed organization and engage with cross-functional teams of experimental and computational...

Join Us in Shaping the Future of Animal Health The Program Lead – Method Remediation (Animal Health) will serve as a subject matter expert, coach and technical team lead driving remediation strategy, prioritizing projects, coordinating resources, and report portfolio status to senior stakeholders. The Program Lead will collaborate closely with Quality Control, Manufacturing Operations, Bioprocess Technology Solutions, Regulatory Affairs, Statistics, and Analytical Technology Solutions across US sites to align priorities, expectations and deliverables. Key Responsibilities Lead complex data analysis and trending to identify non‑robust or out‑of‑specification methods. Conduct biomaterials assessments, inventory reviews, and document gap analyses to define remediation actions....

Role Summary · The Regional Medical Scientific Senior Director Team Lead, RMSD (aka MSL) TL, is a credentialed (i.e., MD, PhD, PharmD, DNP, or DO,) therapeutic and disease expert whose primary role is the leadership, management, and accountability of a field-based team of RMSDs and their deliverables. This Team Lead will manage a team of Immunology – GI focused field medical affairs personnel in the Ulcerative Colitis and Crohn’s Disease TAs. · The RMSD TL ensures team members adhere to Company policies and standard operating procedures (SOPs,) execute on field medical plans, and engage in company research initiatives. The role...

Our Artificial Intelligence and Machine Learning (AI/ML) capabilities are critical accelerators of our mission to invent new medicines that save and improve lives. Core to the Data, AI, and Genome Sciences (DAGS) function is an AI/ML-first approach to improving target and biomarker discovery, validation, and selection, and elucidating complex disease mechanisms. As Director of foundational AI, you will be responsible for leading a team of machine learning researchers and engineers, overseeing both large foundation model development and the development of bespoke methods for extracting insights from noisy biological data. Your work will advance our understanding of complex diseases and support...

About Technology Solutions Our company's Animal Health Technology Solutions offers global animal identification and monitoring solutions for companion animals and livestock. These solutions enable pet owners to better manage the health and well-being of their pets and enable livestock producers to improve well-being and animal production. Technology Solutions include Core Technologies in Livestock Identification, Dairy, Beef and Swine monitoring, for which the product/market fit is established, as well as products in discovery. Our Technology Solutions division is evolving. We are moving to a Product Operating Model – a new way of working that empowers product teams to take full ownership...

Our Artificial Intelligence Machine Learning (AI/ML) capabilities are critical accelerators to our mission of inventing new medicines that save and improve lives. Core to the Data, AI, and Genome Sciences (DAGS) function is an AI/ML-first approach to improving target and biomarker discovery and elucidating complex disease mechanisms. As a senior AI scientist, you will be responsible for extracting biological insights from foundation models, developing new methods for post-hoc and intrinsic explainability of AI models, building rigorous benchmarks, evaluations, as well as fit-for-purpose datasets for answering specific biological questions. Your work will advance our understanding of complex diseases and support the...

Primary activities include, but are not limited to Serves as a Subject Matter Expert in Clinical Programming supporting study build, reporting and analytics. Leads efforts to standardize, simplify, and optimize processes through best practices and continuous improvement initiatives. Provides technical leadership and oversight for Clinical Programming (including reporting and analytics) deliverables across programs, including review of eCRFs, required specification, understanding of Protocol, In-Life Report specifications, and library development. Ensures compliance with established standards, SOPs, and process guidelines while proactively managing timelines and escalating risks related to reporting assets and data flow. Partners closely with study teams, Leadership, and external vendors...

Aligned with the core mission of Global Market Access to expand access to medicines and vaccines to people around the world, this is an exciting opportunity to help lead the development of world-class value-based contracting strategies, solutions, process, and infrastructure. We are seeking a developing leader that is experienced, customer-centric, entrepreneurial, creative, action-oriented, and passionate who thrives in a collaborative team environment. Payors around the world continue to experience growing fiscal tests. Healthcare systems aspire to a more value-based healthcare ecosystem. Industry continues to innovate, and existing payer value assessment pathways are often challenged to properly value these innovations. These...

External Manufacturing Operations Director The External Manufacturing Operations Director provides strategic and operational leadership for products manufactured by external partners supporting the Simtra site in Bloomington, IN. This role is accountable for ensuring reliable, high quality, and compliant supply by overseeing production planning, materials management, quality and technology issues, and day-to-day manufacturing performance. Acting as the primary operational interface with external manufacturing partners, the Ops Director leads issue resolution and escalation, ensures appropriate oversight‑ of shop‑floor activities, and drives continuous improvement initiatives to enhance efficiency, quality, and supply reliability across the network. Responsibilities Provide leadership in dispute resolution with...

Job Location West Point, PA The Department of Pharmacokinetics, Dynamics, Metabolism, and Bioanalytics (PDMB) is seeking a bioanalytical scientist to join our End-to-End Regulated PK & ADA Bioanalytical group located at our research and development site in West Point, PA. Experience in the field of quantitative bioanalysis of small molecules and biotherapeutics, leveraging LC-MS/MS and/or ligand binding methods in a regulated drug development environment, is highly preferred. In this position, you will be responsible for developing bioanalytical methods for measuring biotherapeutics, such as small molecules, monoclonal antibodies, proteins, peptides and antibody-drug conjugates in support of Good Laboratory Practice (GLP) and...

Description The Modality Agnostic Chemistry Scaleup (MACS) Operations group within the Chemical Engineering Research & Development (CERD) Department is seeking a highly motivated individual to work in a fast-paced job that provides a high degree of technical and project management responsibility. The Associate Director – Process/Facility Engineering position will report to the MACS Operations Lead Senior Director as a member of the MACS Operations Team at the Rahway NJ facility. The Associate Director will serve as a technical mentor and process team member supporting the MACS Center, which is a new potent, multi-modality (small molecule, macrocyclic peptides, bioconjugates) Drug Substance...

Our 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 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 to our strategic...

Within Value Chain Management (VCM), the Product Manager will work under the direction of the Value Chain Leader and will support Product Leaders as assigned. The Product Manager may also be directly responsible for a product or portfolio of products. VCM is accountable for our manufacturing division's product strategy in alignment with our manufacturing and global Human Health divisions brand/franchise goals as well as for leading continuous improvement of the product supply chain. Product scope includes new and in-line products within specific Customer Business Lines (Diversified Brands, Biologics, Primary Care, Women’s Health, Oncology, Immunology, Hospital & Specialty, or Vaccines). VCM...

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 Director, AI Innovation Consultant The Opportunity Based in Rahway, New Jersey join a global healthcare biopharma company and be part of a 130-year legacy of success backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Be part of an organization driven by digital technology and data-backed approaches that support a diversified portfolio of prescription medicines, vaccines, and animal health products. Drive innovation and execution excellence. Be a part of a team with a passion for using AI to drive decision-making, and which creates custom software, allowing us to tackle some of...

The Senior Administrative Services Specialist provides proactive, high-quality, flexible and reliable administrative support to the Executive Director of Discovery Process Chemistry in Small Molecule Process Research & Development and their leadership team. This role assists with administrative functions relating to organization and communication across the team and ensures the efficient operation of team members. We are seeking candidates who are proactive and act with a sense of urgency, thrive in complexity, demonstrate resilience, and model the highest caliber of values and standards. Candidates must have an interest in and ability to work successfully in a fast paced, complex work environment....

The Associate Director, Device Quality Assurance within Device Quality & Regulatory (DQ&R) is responsible for providing quality oversight of our Company's Device Network. This specific role is responsible for providing quality support for device assembly and packaging operations at our Company's Wilson, NC site and will be based on-site at Wilson. This role will serve as the primary interface between our Research & Development Division DQ&R and our Company's Wilson, NC site for the following aspects 1. Serve as on-site quality oversight for medical device and combination product operations which require above-site support Accountable for on-site Device Quality and Regulatory...

The Breast Cancer Global Senior Director Medical Affairs (GDMA) is the breast cancer subject matter expert and responsible for driving execution of the Global Medical and Scientific Affairs (GMSA) portion for breast cancer as part of the Global Value & Implementation (V&I) Plans. As a highly specialized SME, they bring business savviness to the organization, are important decision makers and will have a focus on the US, while also supporting the Rest of the World (ROW). The GDMA may also be appointed as a V&I Lead for their disease/asset area, which includes additional organizationally aligned responsibilities. The GDMA works as...

The Enabling Facilities (EF) group within the Chemical Engineering Research & Development (CERD) Department is seeking a highly motivated individual to work in a fast-paced job that provides a high degree of technical and project management responsibility. The Senior Specialist – Manufacturing Automation position will report to the Associate Director, Engineering, Automation Lead position and will be a member of the EF Team at the Rahway NJ facility. EF is responsible for development of new technologies/capabilities, execution of capital and non-capital improvement projects, and the automation system assets spanning production, utility systems and associated infrastructure. Responsibilities of the Senior Specialist...

Senior Manufacturing Automation Engineer — Hybrid (West Point Vaccine Manufacturing) The Senior Manufacturing Automation Engineer is responsible for Life Cycle Management and Connected Instruments for the west point vaccine manufacturing facility. Automation system lifecycle management encompasses the assessment, scoping, funding, and execution of system upgrades to mitigate obsolescence risks and improve cybersecurity posture. This role coordinates with facility automation leads and business capital owners to define upgrade scope, secure capital approval, and manage project delivery. Key automation technologies include Distributed Control Systems (DeltaV), Programmable Logic Controllers (Allen-Bradley and Siemens), OEM process equipment (washers, autoclaves, filter-integrity testers), and purified water systems...

Reporting to the Director of Packaging Commercialization, the Associate Director, Engineering, Packaging Commercialization will lead packaging development for new oral solid dosage and parenteral products in our small molecule portfolio. This role involves collaborating with stakeholders across the end-to-end continuum of CMC areas and requires both an understanding of packaging as well as prior experience developing and commercializing new products on cross-functional teams. The Associate Director will be accountable for the definition and execution of overall packaging strategies that meet global network needs. Responsibilities include ensuring packaging system designs are robust, packaging processes are efficient, and control strategies are integrated...

Principal Scientist / Director, GLOBAL REGULATORY CMC Biologics (R5) Under general supervision of an Executive Director/Senior Director, the Principal Scientist /Director is responsible for developing and implementing Chemistry, Manufacturing, and Controls (CMC) regulatory strategies for our organization's biologics product franchises in accordance with domestic and international regulations and guidance. The Principal Scientist is responsible for the leading the preparation and submission of CMC sections for commercial or new biologics products. The Principal Scientist will lead the development and the implementation of internal regulatory strategies and provides mentoring and coaching to Sr. Scientist and Assoc Principal scientist in support of their...

The Business Unit Engagement Director (BUED), US Oncology will be responsible for managing a team of Campaign Development Leads (CDLs) in the development and delivery of promotional campaigns, customer-centric educational resources, and multichannel assets to achieve business objectives and drive results. Works within and across the US Oncology organization to align on business priorities and translates brand strategy into customer experiences and promotional assets, across relevant channels and media opportunities. Ensures that all promotional work reflects a deep understanding of Oncology customers and their needs, and that these insights are thoughtfully incorporated into credible and compelling customer engagements. Additionally, this...

The successful candidate will play a pivotal role in shaping the future of our CMC (Chemistry, Manufacturing & Controls) digital and data strategy transformation efforts across our R&D division and Manufacturing divisions. The Scientific Associate Vice President role offers a unique opportunity to influence above project/ function strategy, drive digital adjacencies, and ensure connectivity of our data strategy efforts. Join us to make a significant impact on how we leverage data to define process and analytical method development and future data investments for our entire company pipeline. Primary Responsibilities Partner with the Development Sciences & Clinical Supplies (DSCS) Digital Technologies...

Associate Principal Scientist, Regulatory CMC - Biologics (R4) This Associate Principal Scientist position is equivalent to an Associate Director position. Under direction from Director/Executive Director, the Assoc Principal Scientist is responsible for implementing Chemistry, Manufacturing, and Controls (CMC) regulatory strategies for our organization's biologics product franchises in accordance with domestic and international regulations and guidance. The Assoc Principal Scientist is responsible for the preparation and submission of CMC sections for commercial or new biologics products. The Associate Principal Scientist will assist in the development and the implementation of internal regulatory strategies and provides mentoring and coaching to Sr. Scientist /...

Specialist – Manufacturing Automation Description The Enabling Facilities (EF) group within the Chemical Engineering Research & Development (CERD) Department is seeking a highly motivated individual to work in a fast-paced job that provides both technical and project management responsibility. The Specialist – Manufacturing Automation position will report to the Associate Director, Engineering, Automation Lead position and will be a member of the EF Team at the Rahway NJ facility. EF is responsible for development of new technologies/capabilities, execution of capital and non-capital improvement projects, and the automation system assets spanning production, utility systems and associated infrastructure. Responsibilities of the Specialist...

Are you looking for an exciting opportunity with a rapidly growing pharmaceutical manufacturer? If so, then this is the opportunity for you! Under the supervision of the Maintenance and Utilities Supervisor and direction of the maintenance team leader, installs, maintains, tests/certifies, repairs and troubleshoots HEPA filtration equipment. In compliance with operating procedures, Company and Government regulations, and current Good Manufacturing Procedures, assures the quality of our products and services are of the highest priority. HEPA Technicians will perform maintenance on any equipment or facilities which their skills support in a compliant quality manner. HEPA Technicians will work in classified facilities...

POSITION OVERVIEW – Basic Functions & Responsibility Essential functions include, but are not limited to The Associate Technician, Operations is a great entry-level job for recent graduates or those with experience who want to work in manufacturing and packaging. This role involves hands-on activities that support the manufacturing and packaging process. 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 will operate equipment, monitor quality during...

The Screening & Compound Profiling group within the Quantitative Biosciences Department is seeking a Principal Scientist with deep expertise in applied quantitative pharmacology and/or biochemistry to join our Research Laboratories in Rahway, NJ. This role will provide senior-level expertise at the interface of in vitro pharmacology and quantitative modeling. The successful candidate will serve as a scientific resource across the broader research organization, contributing rigorous pharmacological analysis across programs and delivering mechanistic insight to drug discovery decisions spanning target classes, modalities, and therapeutic areas. The primary responsibilities of this role will be to develop, apply, and communicate quantitative data models...

Corporate Paralegal We are seeking an experienced and motivated Paralegal III to join the Corporate Legal team in the Office of General Counsel. The team is responsible for legal and regulatory matters pertaining to our status as a public company, as well as all aspects of corporate governance. The position reports to the Corporate Secretary and also works closely with other team members and internal departments. Responsibilities Securities and Exchange Commission Matters Files and assists in preparing quarterly, annual, and other reports with the SEC (Forms 10 K, 10 Q, 8-K, 11 K, and SD - Conflict Minerals Disclosure). Leads...

The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Immunology therapeutic area. Our company's Immunology 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 assigned 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 trials...

Focus Area Influenza Our Marketing team is passionate about bringing our medicines and vaccines to our customers around the world. Through digital listening and patient analytics, we are able to 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 Digital Human Health organization we are transforming to better power decision-making across our end-to-end commercialization process, from business development to late lifecycle...

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 the design, development, and delivery of efficient, flexible, and modular analysis and reporting and submission standards that can be used for drug and/or vaccine projects across all therapeutic areas. Adheres to standard operating procedures and guidelines established...

This Associate Director, Audit and Assurance Services role will be part of the SOX Project Management Organization (SOX PMO) along with the Director and Executive Director in charge of our SOX Program. This role is responsible for assisting in the development of our SOX Audit Plan, coordinating with external auditors and Global Process Owners, staying connected to the Governance and Compliance Lead who leads any changes to controls, assisting Audit Teams during fieldwork, and ultimately reporting SOX Audit Findings to Senior Leaders. This individual will also assist in audits outside of SOX. Description SOX scoping Develop and maintain the SOX...

Respiratory Sales Sr. Specialist The Respiratory Sales Senior Specialist (RSSS) plays a vital role in bridging the gap between medical products and the healthcare professionals who use them to treat patients. In this role you will develop and manage relationships with a diverse range of specialty health care customers including pulmonologists and other approved specialty physicians, physician assistants, nurse practitioners, nurses, pharmacists, and office managers. Joining this team means being a part of driving meaningful patient impact by utilizing our scientific expertise and serving as the primary contact for customers within your assigned territory which includes Cincinnati, Ohio Key Responsibilities...

In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our 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. This position supports statistical programming activities for multiple and/or large/complex late-stage drug/vaccine clinical development projects. Accountability predominantly includes 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...

The Executive Director, Corporate Audit and Assurance Services will lead and deliver risk-based, value-added internal audit and assurance services. This senior finance and audit leader will partner with business leaders and senior management to assess risks, design and execute complex audits, with a focus on internal controls and compliance. The role combines hands-on audit leadership with people development, project management, and strategic influence. Primary Responsibilities Partner with the Vice President and audit peers to design and implement an annual risk-based audit plan aligned with enterprise strategy. Prepare and present clear, concise audit reports that summarize findings, implications, and recommended actions....

Join our Animal Health Technology Solutions team as the Environmental, Health, and Safety (EHS) Sr. Specialist! You will own compliance programs, partner with site leadership, and drive measurable improvements across our company’s Animal Health Technology Solutions facilities in Dallas, Texas and Baton Rouge, Louisiana! The selected candidate must be open to 30% travel regularly between Dallas, TX and Baton Rouge, LA based on site needs. Responsibilities include but will not be limited to the following main tasks Serve as the primary EHS point of contact for both sites, partnering closely with site leadership, line managers, and cross-functional teams Serve as...

The role of Director, Global Communications, Vaccines is a unique opportunity to join our company, a recognized leader in vaccines, as a key member of the Global Communications Vaccines & Infectious Diseases team. The role is dedicated to managing day-to-day communications related to our company's vaccines portfolio and pipeline. The candidate selected for this role will work under the guidance of the Executive Director, Global Communications, Vaccines & Infectious Diseases, in a fast-paced and ever-changing environment. Responsibilities include, but will not be limited to, the following key activities Primary Responsibilities Lead communications activities in support of several of our company's...

Primary activities include but are not limited to The Associate Principal Scientist is a DVM and/or PhD whose primary function is to design, coordinate, monitor, and report clinical laboratory and field studies that will support the regulatory approval of new companion animal and livestock products. The position requires the candidate be responsible for the conduct of Good Clinical Practice (GCP) studies, and occasionally Good Laboratory Practice (GLP) studies. The Associate Principal Scientist is the primary clinical study team leader and has overall responsibility for a study. The Associate Principal Scientist can also be responsible for several effectiveness studies within a...

of the job 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 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...

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. Position The Executive Director, Regulatory Affairs Liaison reports to the Vice President (VP), General Medicine, and is accountable for defining and executing global regulatory strategy for assigned ophthalmology...

Our Sales team support our customers by providing clinical information about products, educational information, clinical training programs and resources. We support healthcare providers and healthcare systems meet the goals of the patients in their communities. Our Company’s Oncology organization is dedicated to delivering breakthrough innovations that extend and improve the lives of cancer patients worldwide. Our team of dauntless, forward-thinking individuals achieves this through an unwavering commitment to supporting accessibility to medicine, providing new therapeutic procedures, and collaborating with governments and payers to ensure that people who need medicines have access to them. At our company, our focus is on...

We are seeking a dynamic, relationship‑driven leader who can build deep, trusted partnerships with senior business stakeholders and the broader IT organization to deliver measurable value across an Animal Health commercial ecosystem. This role is ideal for someone who excels at navigating complex environments, connecting people and capabilities, and turning strategy into impactful digital outcomes. Role Overview The Animal Health IT Commercial Value Team strategizes and implements digital solutions and services that increase customer engagement, optimize customer experience, and create opportunities for measurable commercial outcomes and incremental revenue, informed by rich, data‑driven insights. In close collaboration across Animal Health IT...

Our Animal Health Division is investing $895 million in expanding our manufacturing and research & development facilities in De Soto, Kansas — the state’s largest economic development project to date. As a Digital lead , you will be part of a world-class team at our Center of Excellence in the Animal Health Corridor, contributing directly to the production of veterinary products that improve animal health and welfare globally. As a Technical Digital lead, you will be given the opportunity to challenge and grow your talents, as well as development of interpersonal and leadership skills to overcome difficult situations and solve...

Principal Scientist – Device Technical and Engineering Lead (Director Equivalent) Our company’s Device Product & Process Development (DPPD) Team designs, develops, and commercializes novel biologic/drug/vaccine - device enabled combination products to achieve safe and effective delivery to their intended site of action. The DPPD Team manages the development of the device constituent of our company’s pipeline of combination products across a variety of therapy areas and routes of administration including inhalation, implantation, and injection. This position will be responsible for applying their knowledge of product and process development in the (bio)pharmaceutical and/or medical device industries to set tactical and strategic...

Director – Global Market Access – Sustainable Access Solutions Private Market Access Sizing Leader Our company is dedicated to ensuring that no patient is left behind. With the paradigm of Universal Health Coverage (UHC) being jeopardized globally, the MFN potential impacts and the growing delays in reimbursement, the private market is becoming of increasing importance. It is therefore crucial to accurately size and forecast private market opportunities. Roles and Responsibilities We are seeking a seasoned, high-talent professional to lead the sizing and forecasting of private market opportunities for pipeline assets. This global role spans all franchises within the Sustainable Access...

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),...

Are you looking for an exciting opportunity with a rapidly growing pharmaceutical manufacturer? If so, then this is the opportunity for you! Our GWES organization is seeking a Manager, Instrumentation and SAP (M1 level) to serve as a subject matter expert (SME) for the Rahway site’s instrumentation, support SAP PM systems supporting utilities and facilities infrastructure, and a manage automation and planning roles within GWES. This role covers the entire site’s facilities instrumentation portfolio and includes planning/design, operations support and planner group management. The ideal candidate brings strong hands-on industrial instrumentation design, installation, and troubleshooting/testing experience. Scope & Impact...

The Chemical Technical Operations Director for North America API External Manufacturing (ExM) leads the Technical Operations team in support of the manufacturing of Active Pharmaceutical Ingredients, intermediates, and drug product intermediates at external contract manufacturing facilities in the region. The successful candidate will provide leadership and expertise in technical oversight, portfolio management, continuous improvement, talent development and upskilling organization capabilities. This position reports to the Executive Director, Chemical Technical Operations (CTO), Small Molecule Science & Technology. The Director of Chemical Technical Operations, as part of the External Manufacturing regional leadership team, is responsible for oversight of external contract manufacturing facilities...

Primary activities include, but are not limited to Assumes the responsibilities for all clinical programing (including reporting and analytics), for standardization, data cleaning and verification including studies and the external data captured in support of the clinical studies. Coordinates and participates in the following activities Oversees and coordinates data reporting activities for multiple clinical programs. Interfaces with leadership to assure consistency of technical and process strategies. Acts as a technical resource to other members of the group along with understanding of Protocol. Plans appropriately to ensure adherence to timelines. Interface with members of study teams and key stakeholders, to integrate...

Primary activities include, but are not limited to Assumes the responsibilities for all clinical programming (including reporting and analytics) deliverables including Oracle, Veeva platforms along with the external data captured in support of the clinical studies. Coordinates and participates in the following activities Design, build, maintain, test, and document data review based on written specifications established by Global Clinical Data Management, Clinical Research and Global Safety. Review the technical feasibility of study team proposed programming/reporting and technically implements them. Work effectively among team to communicate issues and ideas to improve the business along with understanding of Protocol . Support the...

Essential functions include, but are not limited to Requires knowledge and experience in the Quality Control discipline and solves a range of straightforward problems. Analyzes possible solutions using standard procedures. Builds knowledge of the company, processes, testing and customers. Receives a moderate level of guidance and direction and also proactively seeks advice/information from others when addressing serious business issues that may impact other functions. Applies team effectiveness skills, listening and integrating diverse perspectives from across the work group while contributing and adding value to the achievement of team goals. Demonstrates a deep understanding of customer needs, requirements, and expectations. Continuously...

Position within our Company's Global Clinical Supply, Logistics & Regions Trade team. Responsibility for operational and strategic work for compliant US imports/exports ensuring alignment with US CBP, government and health agencies regulations including internal our Company's Global Trade Standards & Controls (GTSC). Position will work in Rahway NJ or West Point, PA and develop strong professional internal and external relationships including but not limited to GCS, GTSC, Customs & International Trade (CIT), our Company's Regulatory, Clinical and Research stakeholders across all our Company's global locations; brokers, carriers ensuring you represent the team and company interests in a professional and collaborative...

Associate Director, Company Production Systems (MPS) Site Support / Global Programs / Lab Transformation With 43 sites around the world, our Company manufactures and distributes critical vaccines, sterile products, biologics, and animal health products to more than 140 countries. Our facilities, along with our external contractors, suppliers, and partners, comprise an interdependent global manufacturing network that’s dedicated to delivering a compliant, reliable supply to customers and patients on time, every time, across the globe. Today, we continue to be at the forefront of innovation in how we make and deliver life-saving medicines and vaccines to better meet the changing...

The Executive Director has the primary responsibility for strategy, oversight, and delivery of end-to-end activities involving new or marketed drug(s) for oncology indications. The Executive Director leads the team responsible for the cross-functional delivery of critical milestones in an oncology asset’s lifecycle, spanning discovery through reimbursement, integrating the scientific, commercial, and manufacturing aspects critical to delivering clinically beneficial medicines to the right patients. The key to success is bearing the primary responsibility for developing, aligning, executing, and communicating the overall asset strategy. Specifically, the Executive Director may be responsible for Creation, alignment, execution, and adaptation of the asset strategy cross-functionally...

Role Summary The Regional Medical Scientific Director (RMSD) is a credentialed (i.e., PhD, PharmD, OD, DO, or MD) 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. The work of an RMSD is aligned to Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights. RMSDs liaise between the scientific community and the Company to enhance the comprehension of scientific foundations and goals for approved,...

Basic Functions and Responsibility As a member of the Site Environmental, Health, and Safety (EHS) team, the Sr. Specialist Industrial Hygiene & Biosafety will provide technical leadership and project ownership to operating departments at the Rahway site with a focus on identifying and anticipating industrial hygiene hazards, supporting biosafety activities, assessing risks, and partnering with operating departments to implement compliant technical solutions. This role provides expert technical support to EHS program owners, leads assigned IH and biosafety projects and studies, and delivers general EHS and laboratory safety support across the site. Integrate EHS programs into daily operations to assure regulatory...

Role Summary The Regional Medical Scientific Director (RMSD) is a credentialed (i.e., PhD, PharmD, OD, DO, or MD) 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. The work of an RMSD is aligned to Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights. RMSDs liaise between the scientific community and the Company to enhance the comprehension of scientific foundations and goals for approved,...

Role Summary The Regional Medical Scientific Director (RMSD) is a credentialed (i.e., PhD, PharmD, OD, DO, or MD) 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. The work of an RMSD is aligned to Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights. RMSDs liaise between the scientific community and the Company to enhance the comprehension of scientific foundations and goals for approved,...

Global Project and Alliance Management (GPAM) sits in the Research and Development organization. The Project Managers and Alliance Managers in GPAM are core members of development and alliance teams. Project Managers drive these cross-functional teams to deliver projects and products that improve human health and our company's business, and Alliance Managers ensure successful collaborations with our R&D alliance partners. Position This position may be based in either Rahway, NJ, or Upper Gwynedd, PA. Under the broad guidance of the AVP/VP, Global Project and Alliance Management (GPAM), the incumbent will spend 50-70% of their time focused on one or more...

Role Summary The Regional Medical Scientific Director (RMSD) is a credentialed (i.e., PhD, PharmD, OD, DO, or MD) 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. The work of an RMSD is aligned to Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights. RMSDs liaise between the scientific community and the Company to enhance the comprehension of scientific foundations and goals for approved,...

Role Summary The Regional Medical Scientific Director (RMSD) is a credentialed (i.e., PhD, PharmD, OD, DO, or MD) 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. The work of an RMSD is aligned to Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights. RMSDs liaise between the scientific community and the Company to enhance the comprehension of scientific foundations and goals for approved,...

Role Summary The Regional Medical Scientific Director (RMSD) is a credentialed (i.e., PhD, PharmD, OD, DO, or MD) 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. The work of an RMSD is aligned to Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights. RMSDs liaise between the scientific community and the Company to enhance the comprehension of scientific foundations and goals for approved,...

Role Summary The Regional Medical Scientific Director (RMSD) is a credentialed (i.e., PhD, PharmD, OD, DO, or MD) 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. The work of an RMSD is aligned to Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights. RMSDs liaise between the scientific community and the Company to enhance the comprehension of scientific foundations and goals for approved,...

Role Summary The Regional Medical Scientific Director is a credentialed (i.e., PhD, PharmD, OD, DO, or MD) 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. The work of an Regional Medical Scientific Director is aligned to Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights. Regional Medical Scientific Director's liaise between the scientific community and the Company to enhance the comprehension of scientific...

Director/Principal Scientist, Devices and Drug-Device Combinations Regulatory CMC Reporting to the Director of Device Regulatory Affairs for Autoinjector Development Programs, the Director/Principal Scientist in Devices and Drug-Device Combinations CMC is responsible to support Device CMC regulatory activities for Our Company’s autoinjector, inhalation, and other delivery system products in accordance with global regulations and guidelines and is responsible for technical content input and coordination of CMC submissions for all assigned activities. Product responsibilities may be in the small molecules, biologics or vaccines portfolio, and could be in the development or the marketed product phase of a drug product life cycle. Primary...

The Chemical Commercialization Technology (CCT) department, which is part of the company's Manufacturing Division, is seeking a self-motivated individual who is looking for an opportunity to work in a highly collaborative environment that provides substantial technical responsibility and leadership of internal and external work. The Senior Scientist, Engineering position leverages scientific/technical experience to develop safe and robust manufacturing processes through process characterization, technology transfer, validation, filing and supply support of late-stage projects in the small molecule pipeline. The candidate will provide scientific expertise by learning and utilizing Quality Risk Management methodologies and tools for statistical design of experiments. This role...

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). A large-scale capital project, known as the FLEx Sterile Expansion project, is currently underway. The FLEx Sterile Expansion project is nearing completion of its detailed design phase and has begun construction and commissioning and...

Role Summary The Regional Medical Scientific Director (RMSD) is a credentialed (i.e., PhD, PharmD, OD, DO, or MD) 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. The work of an RMSD is aligned to Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights. RMSDs liaise between the scientific community and the Company to enhance the comprehension of scientific foundations and goals for approved,...

Role Summary The Regional Medical Scientific Director (RMSD) is a credentialed (i.e., PhD, PharmD, OD, DO, or MD) 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. The work of an RMSD is aligned to Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights. RMSDs liaise between the scientific community and the Company to enhance the comprehension of scientific foundations and goals for approved,...

Role Summary The Regional Medical Scientific Director (RMSD) is a credentialed (i.e., PhD, PharmD, OD, DO, or MD) 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. The work of an RMSD is aligned to Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights. RMSDs liaise between the scientific community and the Company to enhance the comprehension of scientific foundations and goals for approved,...

Role Summary The Regional Medical Scientific Director is a credentialed (i.e., PhD, PharmD, OD, DO, or MD) 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. The work of an Regional Medical Scientific Directoris aligned to Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights. Regional Medical Scientific Director liaise between the scientific community and the Company to enhance the comprehension of scientific foundations...

The Sr. Global Director Medical Affairs (GDMA) is responsible for supporting the execution of scientific & medical affairs plans for Rheumatology in key countries and regions. They are impactful members of Product Development Team sub-teams and Global Human Health commercialization teams. They collaborate with our Research & Development Division's Early and Late Development functional areas, Value & Implementation Outcomes Research (VIOR), Policy, Commercial and Market Access to address opportunities in key countries. They engage with their network of scientific leaders and decision makers. This is a headquarters-based position in Our Company Research Laboratories Value & Implementation Global Medical and Scientific...

The Executive Director, CSRM Device and Product Quality provides strategic and operational leadership for a global Center of Excellence delivering medical and scientific expertise in device safety, health hazard oversight, and product quality medical risk assessment. Reporting to the Vice President, Clinical Safety and Risk Management (CSRM), this role sets clinical risk management strategy, governance, and compliant processes for medical support of devices and combination products across the full product lifecycle. The role is accountable for leading the strategy and implementation of timely medical risk assessment in support of quality issues across developmental and commercial products. The Executive Director leads...