Merck Job Trends

Position Overview - Basic Functions & Responsibility The Global Clinical Supply (GCS) organization, within our Research & Development Division, is accountable for managing the 'end-to-end' integrated clinical supply chain across all of the Research & Development Division portfolio to enable the execution of any clinical trial using our company's asset. GCS supports more than 300 Phase I-IV clinical trials run inhouse, 400+ outsourced or run by partners, as well as our company's IIS clinical trials (200+) and External Collaborations (~200+). GCS is accountable for the planning, sourcing, labeling, packaging and delivery of clinical supplies to clinical sites across more than...

The Manufacturing Operations Specialist will work with the IPT product manufacturing team and partners with the Operations Managers in coordinating production activities and ensure the manufacturing area is operating at peak efficiency. Primary Responsibilities Reporting to the Senior Specialist, Operations, the Operations Specialist primary responsibility will be to help facilitate day to day production and support of operations. He/she will partner with area Manager to assist with ship floor management. This position will require off-shift or weekend coverage based on business unit needs and specific assignments. The successful candidate will be expected to work 2nd shift (4pm-12am), Tuesday-Saturday . The...

Position Objectives We are looking for a driven Cybersecurity Engineer to become a part of our expanding team. This position will be a hybrid position located in Austin, Texas. This role will focus on engineering, deployment, and support of endpoint security solutions. The successful candidate will work closely with global stakeholders to safeguard our company's assets worldwide. The ideal applicant should possess at least 5 years of experience in cybersecurity, with a background in an engineering role within a global environment. Key Responsibilities Implement endpoint security solutions across Cloud, Enterprise, and Manufacturing IT/OT environments. Operate and maintain endpoint security controls,...

Are you ready to make a significant impact in the world of biopharmaceuticals? At our Company, we are at the forefront of innovation in the Manufacturing Division, specifically within the Biologics Drug Substance Commercialization (BDSC) team. Our Downstream Purification department is dedicated to leading the charge in downstream processing for late-stage pipeline and commercial drug substance manufacturing, focusing on life-saving therapeutics. As a Senior Scientist, you will play a pivotal role in shaping the future of biopharmaceutical manufacturing. Working under the guidance of our technical leader in downstream processing, you will collaborate with both internal and external partners to support...

Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety First, Quality Always” mindset striving for continuous improvement. We work in the local plant linked to our global manufacturing network to ensure the highest quality of raw materials, intermediates, and finished products. Our Animal Health team offers veterinarians, farmers, pet owners and governments one of the widest range of veterinary pharmaceuticals, vaccines and health management solutions and services. The Millsboro, DE Animal Health facility is located in Sussex County, DE, within the Salisbury, MD-DE Metropolitan Area. Millsboro is situated at...

Global Project and Alliance Management (GPAM) sits in the R&D organization at our company. GPAM comprises several distinct groups, including Project Managers in Value & Implementation (which is this job), Development, and CMC; Discovery Portfolio Managers; Alliance Managers; Project Management Office (PMO); and Administrative Professionals. Position Description/Summary The GPAM Associate Director, Value & Implementation Project Manager (VIPM), is a core member of Value & Implementation (V&I) Team, partnering with team leaders to develop strategies and execute our Company's drug and vaccine V&I efforts to progress the R&D pipeline and realize its full potential. The Associate Director is expected to provide...

Director, Strategy Execution The Enterprise Strategy Office (ESO) develops, implements, and drives enterprise strategy in support of our company, its customers, and shareholders. The scope of this group includes strategic program management, enterprise strategic planning, risk management, as well as strategic venture investments in healthcare as part of our Global Health Innovation fund. Together, we identify business critical challenges, create and evaluate options, and ensure effective implementation and cross-functional engagement. Position The Director of Strategy Execution plays a crucial role in translating organizational strategy into successful implementation. This involves executing strategic initiatives across the company, collaborating with senior leaders...

The Data Scientist and AI/ML Engineer – Generative AI and Natural Language Processing role involves helping to develop and deploy production-grade NLP products for unstructured and semi-structured data from across our company’s research and development pipeline. These models and workflows will help solve real-world problems and contribute to Artificial Intelligence and Machine Learning (AI/ML) in therapeutic research and development. Key focus areas will include the scalable deployment of ML and Generative AI approaches (such as Large Language Models, or LLMs) for surfacing insights from proprietary unstructured research data and biomedical literature, as well as the integration of structured information from...

Manufacturing Strategy, Business Development and Alliances is responsible for the development and realization of the strategy for the Manufacturing division and oversees the core enterprise manufacturing functions. This includes the Strategy and Portfolio Management office, Global Supply Business Development (GSBD) which evaluates acquisitions, divestitures, and licensing opportunities, Manufacturing Business Alliance Management (MBAM) which manages our regional and global manufacturing strategic partnerships, Network Strategy and Third Party Sales (NSTPS) which oversees the global manufacturing footprint, global product source changes, and Third Party Contract Manufacturing and the Manufacturing Leadership Development Program (MLDP) which recruits and accelerates future talent for the division. The...

Associate Director, Launch Strategy and Operations Location North Wales (Upper Gwynedd), Pennsylvania Division Human Health US (HH-US) Therapeutic Area Immunology

Primary Responsibilities Under the direction of Maintenance Coach, sets up, adjusts, repairs, and maintains all pharmaceutical process equipment Performs calibrations and maintains industrial instrumentation standards Carries out industrial maintenance functions in accordance with current Good Manufacturing Practices and prepares technical documentation on as needed basis Participates in the establishment and improvement of new and existing process equipment. Provides technical specifications and information to Research and Development, Process-Project Engineers, and other Manufacturing Division (MD) requestors Write installs, and tests measuring and non-measuring logic controller programming Primary focus will involve maintaining process equipment by developing/performing PM's, developing/performing instrument calibrations, installing new equipment,...

The Quantitative Pharmacology and Pharmacometrics (QP2) Department of our Company's Research Laboratories in West Point, PA / Rahway, NJ is seeking a curious and collaborative Senior Scientist to support our rapidly expanding cardiometabolic and ophthalmology pipelines. As a senior specialist you will be part of a cr o ss- f uncti o nal te a ms of experienced sci e ntis t s to discover and develop novel therapeutic agents of various modalities for cardiometabolic and ophthalmic diseases. The senior specialist is a skilled quantitative scientist, with a good understanding of the strategic elements of drug discovery and development. The...

Position The Vice President, Regulatory Affairs, General Medicine, will contribute to the mission and vision of the Global Regulatory Affairs and Clinical Safety (GRACS) function of Our Company's Research Laboratories (Research & Development) by Developing an active engagement strategy with US FDA and global health authorities to advocate advanced regulatory strategies for novel medicines. Contributing to the continuous improvement of the operating model for regulatory activities in the US and globally to execute efficiently on regulatory obligations, compliance requirements and company strategy. Providing quality advice to stakeholders creating optimal development, commercialization, and drug/delivery device supply strategies Building our leadership...

The Payments Manager will help lead the strategic direction, operational quality, and innovation of the credit union’s payments ecosystem, including card services, ACH, wires, digital payments, real-time payments (RTP), and emerging fintech integrations. This individual will play a critical role in driving member satisfaction, improving efficiencies, and ensuring regulatory compliance while advancing the credit union’s payments strategy in alignment with its growth objectives. Key Responsibilities Develop and execute the organization’s payments strategy, aligning with overall business goals and member needs. Monitor industry trends, emerging technologies, and regulatory changes to keep the credit union on the cutting edge of payment solutions....

The Quality Assurance Director will provide compliance leadership and direction to our Company and contract manufacturing operation (CMO) sites that manufacture active pharmaceutical ingredients (API), biologics, vaccine drug substances and finished products. As Director, you will support Quality audits and health authority inspections and ensure any resulting corrective and preventative actions (CAPA) are effectively implemented. Primary Activities Serve as a subject matter expert for current good manufacturing practice (CGMP) requirements for vaccine and large molecule manufacturing Partner with our Company and CMO management to identify appropriate CAPA to address findings identified during audits and inspections. Monitor CAPA status and ensure...

Position Overview - Basic Functions & Responsibility The Global Clinical Supply (GCS) organization is within our Research and Development division and is accountable for managing the 'end-to-end' integrated clinical supply chain across our Research & Development division portfolio to enable the execution of any clinical trial using our company's asset. GCS supports more than 300 Phase I-IV clinical trials run in-house, 400+ outsourced or run by partners as well as our company's ISS clinical trials (300+). GCS is accountable for the planning, sourcing, labeling, packaging and delivery of clinical supplies to clinical sites across more than 60+ countries, all in...

The Barrier Operations Technical Operations team is seeking a highly motivated individual to provide technical and engineering support as Senior Specialist of engineering. The successful candidate will have the opportunity to apply their enthusiasm and technical skills as a member of a multidisciplinary team supporting the operation and improvement of a vaccine manufacturing facility with a focus on product franchise support. Responsibilities may include Serves as the subject matter expert (SME) for a liquid vaccine product(s) manufactured within Barrier Operations, and is a member of the product franchise team. This includes formulation and filling. Supports regulatory inspection activities including leading...

Are you driven by a desire to impact the world positively through your professional expertise? As a Manufacturing Operations Specialist with The Manufacturing Operations Specialist is assigned to a product manufacturing team and partners with the Operations Managers in coordinating maintenance activities and ensure the manufacturing area is operating at peak efficiency. Primary Responsibilities Reporting to the Associate Director of Operations or Operations Manager, the Operations Specialist primary responsibility will be to help facilitate day to day production and support of operations. He/she will partner with area Manager to assist with ship floor management This position will require off-shift...

Join 0ur Team of Skilled Tradespeople and Take Your Career to the Next Level! Under the supervision of the Maintenance and Utilities Supervisor and direction of the maintenance team leader, operates, monitors, maintains, and responds to alarms of building utility systems including water chillers, cooling towers, condenser water, high purity water treatment (softeners, de-ionizing and reverse osmosis units and stills), clean steam, building steam and condensate, compressed air and vacuum systems. Maintains logs, necessary paperwork, and completes documentation in a cGMP compliant fashion. Documents work activities completely through work orders and daily labor record. Stationary engineers will perform maintenance on...

The Data, AI, and Genome Sciences (DAGS) department at our company is seeking a highly motivated and skilled data scientist to join our Translational Immunology Analytics team based in San Diego, CA. This individual will play a crucial role in analyzing and interpreting complex multi-omics datasets in immune-mediated diseases generated using various high-throughput platforms. The ideal candidate will possess a deep understanding of computational biology, statistical methods, AI/ML, and bioinformatics pipelines, with a proven track record of independently developing and applying advanced computational approaches to extract meaningful biological insights from integrated multi-omics data in immunologic diseases. This is an exciting...

Wil jij een verschil maken in de biotechsector? Wij produceren hoogwaardige vaccins die het leven van dieren verbeteren en wereldwijd voedselveiligheid bevorderen. Werk met geavanceerde machines in een stimulerende omgeving vol enthousiaste collega’s en sluit je aan bij ons team in De Bilt als Farmaceutisch Operator Welkom in ons team Wij zijn op zoek naar gedreven Farmaceutisch Operators die een scherp oog voor detail hebben en graag willen werken in een innovatieve biotech-omgeving. Op onze productielocatie in De Bilt ontwikkelen we hoogwaardige kippenvaccins die een positieve impact hebben in meer dan 100 landen. Met deze vaccins verbeteren we niet alleen...

Position Description Perform procedures required for testing samples in compliance with current good manufacturing procedures (cGMP), safety and environmental guidelines, including clean room entry and aseptic procedures. Meet testing schedules, which may include working longer hours to complete testing and cleanup. Maintain accurate and compliant documentation. Assist in reviewing and updating current procedures for equipment and processes. Assist in planning, development and implementation of new procedures or special projects, resolution of testing issues by recommending solutions to issue or routes of investigation. Assist in cleaning and sterilization of equipment used in the department as well as cleaning work areas (including...

The Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the Atherosclerosis section of the Atherosclerosis & Metabolism therapeutic area. Our company's Atherosclerosis & Metabolism medicines span all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle of late-stage clinical development and studies, including development strategy, study design, initiation, execution, 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...

Our team in Rahway, New Jersey, is seeking an experienced leader who will manage a team of scientists to support drug substance process development activities to enable and accelerate early and late-stage pipeline programs using fed-batch and continuous manufacturing platforms. The Director, Biologics Process Development (BPD) within the Biologics Process Research and Development (BPR&D) organization is responsible for designing and implementing novel bioprocess technology platforms and processes for upstream and downstream processes that produce high yields along with superior product quality and allow speedy progression for clinical studies and commercial launch. The candidate will be a member of the BPD...

Position The Associate Principal Scientist position will support our Live Virus Vaccines franchises. This broad role includes driving method alignment and supporting consistent executional excellence across multiple testing laboratories, maintaining a robust assay monitoring effort, supporting method procedure life cycle management including automation and/or modernization as applicable, and many other cross functional interactions. This position is technical in nature and demonstrated expertise in vaccine analytics is required. The role also requires effective collaboration with external contract providers as well as colleagues in our research laboratories, supply chain, site and global Quality, as well as CMC-Regulatory. This role will be...

The West Point, PA campus is our Company's largest vaccine manufacturing facility, employing over 2000 individuals. This facility is dedicated to manufacturing bulk and final dosage forms for all our company's vaccine products and is expanding to meet future vaccine demands. The Building 50 Live Virus Vaccine Filling Facility Project team is seeking a motivated individual to join as an Associate Operations Specialist. This position will focus on supporting the start-up of a new vaccine filling and lyophilization facility at the West Point site. The Facility start-up will include design, commissioning, equipment qualification and live virus vaccine drug product process...

Our company is expanding its global recombinant human papillomavirus (HPV) vaccine production network by investing $650 million and have added a 225,000-square-foot building within the footprint of the Maurice R. Hilleman Center for Vaccine Manufacturing in Durham, NC. The new facility is being used to produce the bulk active ingredient for the HPV vaccine, comprised of fermentation, microfiltration/ultrafiltration, and chromatography steps. Approximately 614,000 people are diagnosed with certain HPV-related cancers each year. Our company manufactures the two HPV vaccines that are predominantly utilized to eradicate these cancers globally. In recent years, countries around the world have enacted new or expanded...

of the Job 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...

Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety First, Quality Always” mindset striving for continuous improvement. We work in the local plant connected to our global manufacturing network to ensure the highest quality of raw materials, intermediates and finished products. Position Description This is a night shift position, 12.5 hour ( 600PM – 630 AM ) rotation (2-2-3). The VMF (Vaccine Manufacturing Facility) Associate Production Technician is an excellent entry-level opportunity for recent university graduates or experienced individuals that are interested in working in vaccine production and manufacturing...

Are you looking for an exciting opportunity with a rapidly growing pharmaceutical manufacturer? If so, then this is the opportunity for you! Responsibilities Working in conjunction with all appropriate personnel, performs manual and automated operations, general maintenance and support functions necessary for the production of viral vaccines Maintains, orders, inventories, and transports all required equipment, materials, supplies and products. Ensures shipment criteria and timely availability and delivery Interfaces with the Delta V system and other automated systems (including, but not limited to, LIMS, IMPACT) Performs general maintenance and assists in troubleshooting of equipment. Initiates and documents corrective actions Assists in...

POSITION SUMMARY and SCOPE This position is primarily responsible for running automated / manual laser/ink jet and E.I.D. machines and labeling and packaging products while maintaining quality and safety standards. SPECIFIC RESPONSIBILITIES Responsible for running an automated and manual laser, laser/ink jet or automated E.I.D. marking station to mark Livestock Identification tags as per SOP, labeling and packaging product. Able to understand and comply with Company’s procedures with regards to Health, Safety and Environment. Assist with cleaning laser/ink jet stamping machines as necessary. Assist with equipment failures for corrective actions. Assist with minor machine adjustments as necessary to produce an...

Are you passionate about driving operational excellence in the world of biopharmaceuticals? Do you thrive in managing complex manufacturing operations and solving problems that arise on the shop floor? Here at our company, we're looking for a Manufacturing Operations Manager to join our team. This is your opportunity to be part of a team at the forefront of delivering innovative health solutions. Your expertise could make a real difference. Your Core Responsibilities -You'll dive deep into the shop floor, identifying root causes, analyzing data, and implementing practical solutions to enhance our manufacturing operations. -You will have the opportunity to foster...

POSITION SUMMARY and SCOPE This position is primarily responsible for running automated / manual laser/ink jet and E.I.D. machines and labeling and packaging products while maintaining quality and safety standards. SPECIFIC RESPONSIBILITIES Responsible for running an automated and manual laser, laser/ink jet or automated E.I.D. marking station to mark Livestock Identification tags as per SOP, labeling and packaging product. Able to understand and comply with Company’s procedures with regards to Health, Safety and Environment. Assist with cleaning laser/ink jet stamping machines as necessary. Assist with equipment failures for corrective actions. Assist with minor machine adjustments as necessary to produce an...

As part of Our Company’s Manufacturing Division, within the Bioprocess Drug Substance Commercialization (BDSC), the Cell Culture and Fermentation Sciences (CCFS) department provides the technical process leadership and laboratory capabilities in support of late-stage pipeline and post-market commercial manufacturing processes for vaccines and biologics. CCFS supports various commercialization activities, including process characterization, technology transfer to internal and external manufacturing sites, manufacturing investigations, process validation, and authoring of regulatory submissions. Under the general scientific and administrative direction of Director in the CCFS group and working in conjunction with internal and external partners, this individual will support late stage and commercial program...

The Customer Representative is a key member of the field sales team and plays a critical role in supporting our company's customer centric business model. This position is responsible for working in the North Alabama, Tennessee, Kentucky, and Georgia territories to understand and identify customer needs, by selling our company's Animal Health products, supporting pull-through activities relative to the customer strategy, and ensuring that our company's Animal Health is viewed as bringing value and technical innovations aligned to our strategic focus the Science of Healthier Animals. In addition, the Customer Representative demonstrates an understanding of the resources available across our...

This second shift, Monday to Friday 200pm - 1030pm, Technician position is available at the Animal Health facility in De Soto, Kansas, located near Kansas City metropolitan area. The DeSoto facility is expanding operations to manufacturing vaccines and biologics for large and companion animals. Leveraging an experienced and innovative team environment, the key technologies at the site are biologics production using fermentation and cell culture platforms, filling and packaging. The De Soto facility is part of our global Animal Health Manufacturing Division network and is a key contributor to the manufacturing of animal health products. Working within one of the...

Senior Maintenance Specialist P2 Days Primary Responsibilities Reporting to the Associate Director of Maintenance and Engineering or the shift Maintenance Manager, the Maintenance Specialist primary responsibility will be to help facilitate day to day Maintenance and Metrology operations in support of DS4 manufacturing operations. This role actively supports, participates, and embraces an inclusive team culture, including interaction with Operations, Quality, Automation, Technology, and other groups as required. The candidate will cover scheduled time off for managers as needed to ensure continuous operation and support. Furthermore, this role will help manage projects to drive improvements and efficiencies within the facility. The...

The West Point, PA campus is our company's largest vaccine manufacturing facility with more than 2000 employees. This facility manufactures bulk and/or final dosage forms for all of our company's vaccine products and is growing to meet the vaccine demands of the future. The Building 50 Live Virus Vaccine Filling Facility Project team is seeking a highly motivated individual to fill an open position to lead the start-up of a new vaccine filling & lyophilization facility at the West Point site. Facility start-up will include design, commissioning, equipment qualification and live virus vaccine drug product process demonstration in support of...

Our IT team operates as a business partner proposing ideas and innovative solutions that enable new organizational capabilities. We collaborate globally to deliver the services and solutions that help everyone to be more productive and enable innovation. Join our innovative IT team at our company, where we leverage technology to enable new organizational capabilities. We are seeking a Product Analyst to be a change agent for our order-to-cash process. This role offers the opportunity to lead and execute key projects and change initiatives within Order Management, Customer Master and digitization in order-to-cash area. Responsibilities Directly coordinate, align, and partner with...

Our Clinical Development teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs and new indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific and ethical standards. The Distinguished Scientist (Executive Director) and Product Development Team (PDT) lead, Oncology Global Clinical Development, has primary responsibility for the planning and directing clinical research activities involving new or marketed drugs in the Oncology Clinical Research group and in the field of gastric and esophageal cancers . The Executive Director, PDT lead will manage...

Join us as the Quality Center of Excellence Lead at our Wilmington Biotech site, where you'll shape the future of breakthrough medicines by ensuring top-tier quality and compliance with global regulations. Lead a high-performance team, drive commissioning and validation excellence, and collaborate globally to deliver life-changing therapies right first time to patients worldwide. If you have 10+ years in Quality Assurance and a passion for innovation and leadership, this is your opportunity to make a global impact. & SPECIFIC OBJECTIVES The Quality Center of Excellence (COE) Lead role will involve establishing the Quality COE structure at the Wilmington Biotech...

Our Clinical Research and Pharmacovigilance team pushes the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine. The Senior Principal Scientist/Senior Director is responsible for protocol development and medical/scientific oversight of clinical research studies involving new or marketed drugs in the Vaccines Clinical Research group. He/she will be responsible for all phases of the trial process, including but not limited to the design, oversight and medical monitoring of Phase I to V clinical trials, preparation of progress reports...

BPR&D Downstream Principal Scientist Our Scientists are our Inventors. Using innovative thinking, state-of-the-art facilities, cutting-edge science, and technology , we partner to deliver the next medical breakthrough. We are seeking a collaborative, self-directed learner with a penchant for problem-solving and expertise in downstream bioprocessing to join Biologics Process Research & Development (BPR&D) as a Principal Scientist. BPR&D within our company's Research Lab oratories is on a mission to rapidly deliver diverse biotherapeutics to patients by efficiently developing innovative, robust manufacturing processes and technologies. To achieve th is, we work closely with colleagues in Discovery, Pre-clinical, Early Development, Analytical, Formulation,...

The Associate Vice President (AVP)/Section Head, Global Clinical Development, Pediatrics will focus on driving strategy, development, and life-cycle management activities for pediatric vaccines in the Therapeutic Area. The incumbent will be expected to lead multiple programs that are in various stages of development therefore requiring someone who has late vaccine clinical development and lifecycle management experience. The AVP will also be responsible for guiding Clinical Directors within their group to ensure that the programs within their Section are being executed effectively according to approved strategies and plans. They will require a solid understanding of various diseases, the functions and processes...

Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety First, Quality Always” mindset striving for continuous improvement. We work in the local plant connected to our global manufacturing network to ensure the highest quality of raw materials, intermediates and finished products. The Maurice R. Hilleman Center for Vaccine Manufacturing is located in Durham, NC. This state-of-the-art facility established in 2004, manufactures our Company lifesaving vaccines in bulk and finished forms. Due to the importance of this facility in our Company Vaccine Manufacturing network, the facility has seen rapid growth...

The Regional Director Medical Affairs (RDMA) is responsible for driving execution of scientific & medical affairs plans for their assigned Therapy Areas (TA) in the countries of their assigned region. They are impactful members of regional cross-functional teams, including regional Commercial, Center of Real-World Evidence (CORE), Policy and Market Access. They engage with their network of scientific leaders in their region. This is a regionally based position (i.e. residing in one of the affiliates of the region or regional hub) in Our Company Research Laboratories Global Medical and Scientific Affairs (Research & Development (R&D) GMSA). Responsibilities and Primary Activities Guides...

We are seeking an experienced Technical Product Manager to lead the development and management of our OMICS data product portfolio. This unique role combines a strong understanding of biopharma research, hands-on experience with various OMICS modalities, and the ability to drive product strategy and execution. Successful candidate will be accountable for timely availability of OMICS data for in silico research and ensure that our data products meet the evolving needs of researchers in the field. Key Responsibilities Collaborate with stakeholders to understand their OMICS data needs for in silico discovery, defining the core capabilities required to support these needs. Develop...

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...

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...

Senior Specialist, Quality Assurance The Quality Assurance team ensures that every material used in our products is manufactured, tested, packaged, stored, and distributed according to high standards of quality and in compliance with all regulatory requirements. The Senior Specialist, Quality Assurance will support ongoing efforts to supply the market by providing quality oversight for Validation, Plant Engineering, and Deviation Management activities related to drug substance and drug product manufacturing. Position Responsibilities Reporting to the Associate Director, Technical QA, the Senior Specialist, QA Technical will independently manage assignments related to compliance with cGMP regulations and our Company’s Quality Management System. Responsibilities...

Our Digital Manufacturing Operations organization supporting the flourishing 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 experienced and skilled Distinguished Scientist to join our Device Development & Technology (DD&T) organization to serve as a senior technical subject matter-expert and advisor for our Autoinjector platform. This role’s scope and accountability will encompass the entire lifecycle from early development through lifecycle management, providing critical technical strategic oversight and guidance across all teams involved in the development and support of Autoinjectors. The ideal candidate will possess extensive knowledge in medical device engineering, particularly in the design, manufacturing, and regulatory aspects of Autoinjectors and combination products. Primary Responsibilities Technical Strategic Oversight Provide deep...

Are you looking for an exciting opportunity with a rapidly growing pharmaceutical manufacturer? If so, then this is the opportunity for you! We are seeking a Growth and Improvement minded Automation Engineer that can help drive our Strategic Operating Priorities. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement, and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. Our engineers support...

As part of Our Company’s Manufacturing Division, and within the Vaccine Drug Substance Commercialization (VDSC) department, the Bioconjugation and Chemistry (BCC) team provides the technical process leadership and laboratory capabilities in support of late-stage pipeline and post-market commercial manufacturing processes for biologically derived drug substances (e.g., therapeutic proteins, antibody drug conjugates, or vaccines) generated from bioconjugation processes. For late-stage pipeline commercialization, activities include process characterization, technology transfer to internal and external manufacturing sites, process validation, and authoring of regulatory submissions. For commercial programs, activities include site-to-site process transfers, manufacturing investigations and trend evaluations, process enhancements, next generation process development and...

Join Our Team of Skilled Tradespeople and Take Your Career to the Next Level! Under the supervision of the Maintenance and Utilities Supervisor and direction of the maintenance team leader, installs, maintains, operates, calibrates, repairs and troubleshoots refrigeration, air conditioning and air volume equipment and associated control systems. 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. HVAC mechanics will perform maintenance on any equipment or facilities which their skills support in a compliant quality manner. HVAC mechanics are part of the...

The Oncology Regional Medical Scientific Director, RMSD, is a credentialed (i.e., PhD, PharmD, DNP, MD) therapeutic and disease expert who engages in scientific exchange with leaders in the external medical and scientific community. RMSDs provide to Scientific Leaders (SLs) balanced, factual, scientific information about non-product areas of interest to the company. RMSDs reply to scientific questions from SLs, including questions about company products. The work of an RMSD is aligned to core pillars Scientific Exchange, Clinical Research, Scientific Congress Support, and Scientific Insights. Location This MSL-type role is a remote position that serves the territory of TX & OK. This...

Customer Engagement Planning and Measurement - Business Unit Leader – US Market The Customer Engagement Planning and Measurement - Business Unit Leader will be a key member of the leadership team, responsible for guiding a group of Customer Engagement Architects. This Director-level position focuses on developing and executing cohesive omnichannel strategies to enhance customer engagement and optimize marketing operations in the US market. This role will work closely with Brand Marketing and Sales leadership to align digital customer strategies and promote a culture of continuous improvement and innovation. Key Responsibilities include Team Leadership and Development Lead and mentor a team...

The mission of our company’s Research Laboratory Quality Assurance is to safeguard the rights and well-being of patients; the welfare of animals; comply with applicable global regulatory requirements through sound processes and procedures, and to provide independent assurance that delivers high quality data and clinical supplies. The Compliance and Quality Management Systems (CQMS) organization is part of the larger Global Development Quality (GDQ) organization within our company's Research Laboratory Quality Assurance and is accountable for the execution of critical activities in the areas of compliance, quality systems, regulatory intelligence, and the Quality Management System (QMS). The Global Quality Systems role...

Machine Learning Engineer (MLOps) Technical Lead, Data Science and Scientific Informatics The Data Science and Scientific Informatics Team at Research and Development Sciences IT (RaDS-IT) of our company is seeking a Lead Machine Learning Engineer for MLOps. The successful candidate will engage in exploration, design, and implementation of features to support new MLOps use cases for a growing and diverse range of models and platforms. This role will involve the deployment and operationalization of machine learning models across multiple domains, ensuring that our analytics capabilities are robust and scalable. Responsibilities Serve as MLOps representative to stakeholders and lead discussions with...

Our Human Health Digital Data and Analytics (HHDDA) team is innovating how we understand our patients and their needs. Working cross functionally we are inventing new ways of engaging, interacting with our customers and patients leveraging digital, data and analytics and measuring the impact. The Associate Director, Global Commercial Pharma Pipeline Analytics, HHDDA will be responsible for developing and delivering data and analytics, generating strategic insights, and addressing US new product teams’ business questions to inform pharma pipeline investments, a successful go-to-market strategy and creating synergies with the book of work for global brand leads. Furthermore, the team member will...

We are inspired by the belief that a research-driven enterprise dedicated to scientific excellence can create medicines that save and improve lives. Every employee is building on our proud legacy of scientific breakthrough. Our ability to impact the lives of patients worldwide depends on the integrity, creativity, humility, and scientific acumen of our team. We are creating a diverse organization that is inspired by invention and founded on a culture of respect and collaboration. At our Research Labs in South San Francisco, you’ll have the opportunity to expand your knowledge and skills through collaboration with talented and dedicated colleagues while...

This position resides within our company's Value and Implementation (V&I), Outcomes Research organization, which is responsible for real-world evidence generation and outcomes research to enable sustained patient access to our company’s innovations and improve patient health outcomes. Under the guidance of a senior leader, this individual will support one or more V&I, Outcomes Research teams across the Lung Cancers program. Primary Responsibilities Support the value evidence team in Lung Cancer and contribute to value evidence strategies for in-line and pipeline products. Serve as outcomes research representative on cross-functional regional and global teams. Critically assess drivers and barriers to reimbursement and...

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. Our team in Rahway, New Jersey, is seeking an exceptional leader who is passionate about leading a team of Scientists to deliver analytical solutions that enable and accelerate process and product development and manufacturing and ensure safety and quality of our products. The successful candidate will be...

Associate Principal AI/ML Engineer Our Artificial Intelligence Machine Learning (AI/ML) capabilities are critical accelerators to our mission to delivering towards 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, validation and selection and elucidating complex disease mechanisms. As Associate Director, AI/ML Engineering, you will build state-of-the-art AI/ML tools and pipelines to accelerate scientific discovery. You will be part of a cross-functional team of computational biologists, bioinformaticians, data scientists, software engineers, and other AI/ML engineers that strive to identify therapeutic targets. Primary...

The Aircraft Maintenance Technician is responsible for performing inspection, repair, and maintenance of company-owned aircraft in accordance with the aircraft manufacturer's recommendations, FAA regulations, and departmental policies. The ideal candidate will work closely with other team members to ensure the safety and airworthiness of the aircraft, while maintaining accurate maintenance records. This position will be on a schedule rotating between first and second shift. Key Responsibilities Aircraft Maintenance Conduct scheduled and unscheduled inspections, repairs, and maintenance on airframes, engines, and auxiliary power units (APUs). Perform troubleshooting of aircraft systems to identify and rectify discrepancies. Maintenance Records Management Maintain accurate and...

The West Point Technical Operations Laboratory Process Support group within our Company Manufacturing Division is responsible for supporting all commercial vaccines with best in class laboratory support for technical investigations, lifecycle-management driven process enhancements , and commercial vaccine expansions. We are seeking an experienced Associate Principal Scientist to join the Live Virus Vaccines Lab in West Point, PA. The candidate will have a primary role on a team providing laboratory scale manufacturing process support for our Company’s portfolio of licensed live virus vaccines . The candidate will collaborate with key stakeholders to design, execute on, and analyze experiments to enhance...

Grâce à notre engagement envers The Science of Healthier Animals®, nous offrons aux vétérinaires, aux agriculteurs, aux propriétaires d’animaux et aux gouvernements une des plus vastes gammes de produits pharmaceutiques vétérinaires, de vaccins et de solutions et services de gestion de la santé, ainsi qu’un vaste éventail de produits d’identification, de traçabilité et de monitoring en élevage . Nous investissons grandement dans des ressources dynamiques et complètes en recherche et développement et dans une chaîne d'approvisionnement mondiale moderne. Nous sommes présents dans plus de 50 pays, et nos produits sont offerts dans environ 150 marchés. Secteur Sud-ouest Description Générale...

Director, Global Commercial Pharma Pipeline Analytics, Ophthalmology, HHDDA Our Human Health Digital Data and Analytics (HHDDA) team is innovating how we understand our patients and their needs. Working cross functionally we are inventing new ways of engaging, interacting with our customers and patients leveraging digital, data and analytics and measuring the impact. The Director, Global Commercial Pharma Pipeline Analytics, HHDDA will be responsible for developing and delivering data and analytics, generating strategic integrated insights, and proactively addressing global brand leads and US new product team’s business questions to inform pharma pipeline investments and launch readiness. Furthermore, the leader will partner...

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 Market Access Oncology, lead the pipeline TROP 2 asset in combination launches for across multiple solid tumors. In this capacity, the candidate will lead all Oncology global market access and pricing activities, including asset access strategy work, development of payer value proposition messages as well as payer value tools leading up to launch and after. As an asset lead, the candidate would need to synthesize...

The Senior Scientist, Device Design Control Lead, is a crucial member of our team, responsible for spearheading design control efforts in combination product development, commercialization, and lifecycle management. This individual will oversee device design control activities to ensure the delivery of high-quality products and efficient manufacturing processes. The role requires extensive collaboration with subject-matter experts across various cross-functional combination product development teams throughout all phases of the product lifecycle, from concept through launch and post-market surveillance. Key Responsibilities and Activities The Senior Scientist, Device System – Device Design Control will be responsible for device design control activities in the following...

The Quantitative Pharmacology and Pharmacometrics (QP2) Department of our Company's Research Laboratories in West Point, PA / Rahway, NJ is seeking a curious and collaborative Associate Director to support our rapidly expanding cardiometabolic and ophthalmology pipelines. As an Associate Director, you will represent QP2 on cr o ss- f uncti o nal te a ms of experienced sci e ntis t s to discover and advance the clinical development of novel therapeutic agents for cardiometabolic and ophthalmologic diseases. You will work on the discovery and development of small molecules, biologics and non-traditional therapeutics like peptides, novel biological constructs, and others....

Function Under the supervision of Director(s)/Manager(s), performs clerical, administrative, and related duties Equipment for example but not limited to Fax, copier, printer, computer, MVX, teleconference/video equipment, shredder, delivery services, scanner Key Responsibilities Responsible for fundamental administrative/clerical duties requiring analytical ability, independent judgment and problem-solving skills Review priorities with management as necessary Responsible for mail distribution and collection, phone coverage, copying, scanning, and basic expense reports and/or routine financial disbursements Requires basic knowledge of Company policies and practices Apply knowledge and understanding of standard operating procedures for the organization and Division, as well as, specialized terminology commensurate with the position Interact...

Our company's Animal Health is seeking a motivated individual to work as a bioanalytical bench scientist within its Good Laboratory Practices (GLP) bioanalytical laboratory. This is a bioanalytical scientist position with primary duties in preparing and analyzing samples from biological matrices using LC-MS/MS, and preparing reports. This position is a part of the Bioanalytical group, Global Preclinical Development, based in Rahway, New Jersey. Main responsibilities include Development, validation and implementation of LC-MS/MS assays for the analysis of tissue, plasma and other biological samples to support pharmacokinetic, toxicokinetic, clinical efficacy and/or human food safety studies in a GLP environment, with duties...

Primary Purposes and Functions The Clinical Veterinarian is responsible for providing additional veterinary oversight for the care and use of animals at the De Soto, KS research facility and other locations as needed. They will be responsible for ensuring that procedures are humane, legal, ethical, and efficient. Responsibilities also include training and potential membership on the IACUC. The Clinical Veterinarian will also support the Attending Veterinarian with management of the clinical research facilities and staff. Management duties include but are not limited to supervising direct reports, dotted line oversight of animal caretakers, farm oversight, equipment oversight, etc. The Clinical veterinarian...

Our Engineers support internal and external manufacturing operations to remain operational, continuously improve and innovate. With our extensive range of facilities and environments, our Engineers have opportunities across many diverse areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation. Our company is expanding its global recombinant human papillomavirus (HPV) vaccine production network by investing $650 million and have added a 225,000-square-foot building within the footprint of the Maurice R. Hilleman Center for Vaccine Manufacturing in Durham, NC. The new facility is being used to produce the bulk active ingredient for the HPV vaccine,...

The individual in this role will be responsible for maintaining equipment data, calibrations and unplanned repair activities, documentation, schedule adherence, working with customers, analyzes equipment performance, and assist in writing maintenance/calibration work instructions. The Senior Calibration Technician will use computerized systems such as ProCal for data entry and report generation. The Senior Calibration Technician will also use systems related to maintenance such as MES, Delta V, and other software systems. Primary Activities Communicate effectively to Operations and scheduling personnel. Able to prioritize scheduled work. Self-motivated, applies knowledge, and skills to other areas within the department; provides technical guidance and training...

Director, Combination Product Regulatory CMC - (R5) This Principal Scientist position is equivalent to a Director position. Under direction from the Combination Product Regulatory CMC Team Leader, the Principal Scientist is responsible for executing in the Regulatory CMC space. Leveraging demonstrated capability in Regulatory CMC, this candidate will contribute to and implement Device and Drug-Device Combination regulatory strategies for our organization in accordance with domestic and international regulations and guidance. The Principal Scientist is responsible for the preparation and submission of combination product sections of regulatory submissions, correspondences, etc. for commercial and development products. Focus of support will be most...

The Director, Global Scientific and Value Content-Healthcare Professional (Dir GSVC-HCP) for oncology is a headquarters-based leadership role within Global Medical and Value Capabilities (GMVC) organization. The role reports directly to the Therapeutic Area (TA) Team Lead, GSVC. The role has several key responsibilities with in the Global Medical and Scientific Affairs (GMSA) team. These responsibilities highlight the comprehensive and collaborative nature of the role, emphasizing leadership, strategic planning, and cross-functional engagement Engaging with Key Stakeholders Proactively to create and adapt the GMSA Value & Implementation (V&I) Planning & Scientific Platform. This platform provides the framework for GSVC Annual Product...

The Engineering and Maintenance team enables our manufacturing operations to provide a reliable supply of medicine for our patients. The Engineering and Maintenance team members have opportunities to work cross functionally with many diverse areas including Biological, Chemical, Automation, Capital Projects, Safety, Process Development, Technical Services, Utilities, and Validation. We are seeking a Maintenance Manager in Durham, North Carolina to manage a team of maintenance personnel. The Manager will provide direction and technical guidance to maintenance technicians for a capital project startup. In this role you will actively manage your team to reliably support customer demand (including employee development, routine...

The Technician position is available at our Animal Health facility in Worthington, Minnesota. The Worthington facility is expanding operations to manufacture vaccines for large and companion animals. Leveraging an experienced and innovative team environment, the key technologies at the site are biologics production using fermentation and cell culture platforms and filling and freeze-drying. This position will help with the preparation of intermediate components (media solutions, working seed stocks and bacterial antigens), and the downstream processing of the intermediate components. Duties include but are not limited to Position prepares media, will work with fermentation vessels called Bellco's, and perform necessary cleaning/disinfecting...

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 late-stage drug/vaccine/neuroscience clinical development projects. This may include leadership of one or more projects. Accountability predominantly includes the development and execution of statistical analysis and reporting deliverables (e.g. safety and efficacy analysis datasets, tables, listings,...

of the Job Our Sr. 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...

The Quantitative Pharmacology and Pharmacometrics (QP2) department drives model-informed drug discovery and development (MIDD) to routinely enable efficient drug discovery/development and/or regulatory decisions. The Pharmacometrics group within QP2 brings an experienced leadership team, deep modeling expertise and state-of-the-art modeling approaches across multiple therapeutic areas and modalities to drive portfolio impact from discovery through life-cycle management. The team is externally visible and continues to be at the leading edge of building innovative tools. With MIDD as an essential component of decision-making at our Company, this position offers an opportunity for the Pharmacometrics leader to drive pipeline impact and lead a talented...

Senior Principal Scientist Translational Medicine, Immunology Translational Medicine in our Research & Development Division is responsible for planning and management of an important inflection point in the drug development process, working closely with scientific, regulatory, statistical, and modelling colleagues across the organization to translate the benchtop science of preclinical discovery into compounds ready for assessment in large clinical populations. We are seeking a highly qualified physician-scientist with a proven track record in the pharmaceutical industry as well as independent academic research for a position in our group. The preferred candidate will have at least 5-year experience in the pharmaceutical industry...

Our Engineers support internal and external manufacturing operations remain operational, continuously improve and innovate. With our extensive range of facilities and environments, our Engineers have opportunities across many diverse areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation. Director Global Engineering Services Construction and Logistics Director is responsible to support a $3B capital program. Guide teams to carefully plan, identify risks and mitigation strategies, track and monitor progress, escalate risks and cascade information. Align a cross-functional team around the project mission/work plan. Interface and align with key Service Providers of Engineering, Procurement, Equipment,...

We are seeking an experienced talented scientist to join the Quantitative Pharmacology and Pharmacometrics – Immune/Oncology (QP2-IO) team in the role of Associate Director, Quantitative Systems Pharmacology (QSP) . QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects related to clinical pharmacology, mechanistic PK-PD modeling and pharmacometrics of oncology drugs from post-PCC to registration. As a subject matter expert, the Associate Director within the QP2-IO Group will work closely with teams of highly collaborative, cross-functional scientists to contribute to the development of novel therapeutics. They develop strategies for quantitative analyses (and commensurate...

Role Summary The Regional Medical Scientific Director is a credentialed (i.e., PhD, PharmD, DNP, 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 liaise between the scientific community and the Company to enhance the comprehension of scientific foundations and...

The Quantitative Pharmacology and Pharmacometrics (QP2) Department of our Company's Research Laboratories in West Point, PA / Rahway, NJ is seeking a curious and collaborative Associate Director to support our robust infectious disease and vaccines pipeline. As an Associate Director, you will represent QP2 on cr o ss- f uncti o nal te a ms of experienced sci e ntis t s to discover and advance the clinical development of novel small molecules, biologics, and vaccines for infectious diseases. The Associate Director is a skilled quantitative drug developer, with a strong, integrated understanding of the strategic elements of drug discovery...

The Regional Medical Scientific Director (RMSD) is a credentialed (i.e., PhD, PharmD, DNP, 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, in-development, and active Company-sponsored...

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 provides high quality statistical programming analysis and reporting deliverables for global PK modeling and simulation stakeholders for Oncology therapeutic area. The programming analyst will gather and interpret user requirements, retrieve the required data, transform the data into modeling-ready...

Role Summary The Regional Medical Scientific Director (RMSD) is a credentialed (i.e., PhD, PharmD, DNP, 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, in-development, and...

Position Responsibilities The Regional Medical Scientific Director (RMSD) is a credentialed (i.e., PhD, PharmD, DNP, 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, in-development, and...

Role Summary The Regional Medical Scientific Director is a credentialed (i.e., PhD, PharmD, DNP, 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 liaise between the scientific community and the Company to enhance the comprehension of scientific foundations and...

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 The Senior 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 development projects. Accountability predominantly includes submission data standards planning activities,...

Position Overview The Global Supply Chain Management Regional Operations team is responsible for ensuring inventory is consistently available to meet customer demand using data analytics. The role requires partnership with numerous stakeholders including but not limited to Commercial, Site Operations, Finance, and other manufacturing and supply chain support functions, all in order to build robust demand and supply plans to ensure customers receive the right amount of product at the right place, at the right time. This individual will spend approximately six months in the Site & Market Support Role, before moving into the Network Strategy Execution Role within the...

Position Responsibilities The Regional Medical Scientific Director (RMSD) is a credentialed (i.e., PhD, PharmD, DNP, 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, in-development, and...

Position Description We are seeking an experienced and skilled Cheminformatician and AI/ML data scientist to join the Cheminformatics group within Modeling and Informatics (M&I) at our Boston/Cambridge, sites. This role requires exceptional interpersonal and problem-solving skills, as well as the ability to translate scientific needs into actionable plans for implementing data workflows and infrastructure that accelerate the decision-making process from hit identification to clinical candidate delivery across different therapeutic areas and modalities at our company. M&I is a diverse and inclusive team within the Research Laboratories Discovery Chemistry organization, comprising approximately 60 computational chemists, cheminformaticians, and data scientists. We leverage...

The individual in this role will be responsible for maintaining equipment data, calibrations and unplanned repair activities, documentation, schedule adherence, working with customers, analyzes equipment performance, and assist in writing maintenance/calibration work instructions. The Senior Calibration Technician will use computerized systems such as ProCal for data entry and report generation. The Senior Calibration Technician will also use systems related to maintenance such as MES, Delta V, and other software systems. Primary Activities Communicate effectively to Operations and scheduling personnel. Able to prioritize scheduled work. Self-motivated, applies knowledge, and skills to other areas within the department; provides technical guidance and training...

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

The Associate Principal Scientist is a DVM/VMD 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 project, participating as the clinical representative in project...

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

The Lead Maintenance Technician position will supervise and work actively in a dynamic production dedicated maintenance team supporting the Plant Maintenance and Production departments. The Lead will focus on installation, modification, troubleshooting, removal, and repair of hydraulic, pneumatic, electrical, and mechanical components of critical production equipment. Critical systems that are in scope for the Lead’s team will include, but not be limited to Bosch/Syntegon sterile filling lines, Cozzoli Sterile filling lines, West/Genessis capping lines, Brenton robotic packaging lines, Weiler labeling systems and Blending tanks. The Lead will be seen as the driver of safety and compliance for activities on and...

The Livestock Technology Solutions Customer Success Specialist will be the lead in delivering and developing training for end customers, distributors (train the trainer), and distributor representatives. This position will be responsible and accountable for training end user to successfully enter, interpret and analyze all aspects of sensor technology data including reproduction, health, and milk as well as assist the customer and their staff on the change management journey related to the implementation of our products. Our data-driven solutions are used by farmers, companies, and countries to manage hundreds of millions of animals worldwide. By putting intelligent, actionable management information into...

The Future Talent Program features internships that last up to 12 weeks and will include one or more projects. These opportunities in our Information Technology division can provide you with great personal and professional development. About Our Company’s Information Technology Division (IT) Our IT teams operate as business partners proposing ideas and innovative solutions that enable new digital and technological organizational capabilities. We collaborate internationally to deliver services and solutions across our organization. We’re looking for emerging talent who have a passion for applying technology to enable healthcare, are able to work on a team as well as independently, and...

The IT Emerging Talent Rotational (ETR) Program cultivates the technical, business, and professional experience of entry-level technologists. Working in teams alongside highly skilled professionals, ETR employees apply their passion for technology to help our company develop and provide innovative products and services aligned to our most critical business outcomes. Over the course of 2 years, as an IT ETR, you will explore 3 different roles and areas of IT. We’re looking for emerging talent who have a passion for applying technology to invent novel life-saving drugs, broaden access to medicines and vaccines, and enable next-generation healthcare solutions. Potential rotational opportunities...

The West Point Quality organization ensures our products are manufactured, processed, tested, packaged, stored, and distributed aligned with our incredibly high standards of quality and meets all regulatory requirements. Partnering across our West Point campus, internal manufacturing facilities, external contract manufacturers and suppliers we create a global manufacturing network dedicated to deliver a compliant, reliable supply to customers and Patients on time, every time, across the globe. The Quality Compliance Director will be a core member of the West Point Quality Assurance Leadership Team and serves as a quality leader accountable for the quality oversight and management of the Quality...

The Data Science and Scientific Informatics Team at Research and Development Sciences IT (RaDS-IT) of our Company is seeking a Lead Data Scientist for Representation Learning. Our team is a diverse collection of scientists and engineers working towards the same goal – enabling and accelerating the next generation of pharmaceutical sciences. We collaborate closely with laboratory and in silico scientists, proposing and implementing innovative solutions that enable new organizational capabilities. An ideal candidate will have a strong background in computational biology, machine learning, and chemistry, with a focus on developing and applying advanced methods for molecular and protein design. This...

Join Our Team as the Associate Director of Digital External Manufacturing & Supply Chain! Are you a strategic thinker with a passion for driving digital transformation in manufacturing? Our Company is on the lookout for a dynamic External Manufacturing Digital Product Manager to become a key part of our Digital Manufacturing Organization within the Supply Chain Planning Product Line. Come and join our journey to innovate and connect with our global partners to enable end to end visibility of our products ensuring our Company delivers quality compliant supply to our patients. In this pivotal role, you will lead the charge...

of the Job Our Sr. 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...

Délégué Vétérinaire secteur Paris et Ile de France 75, 92, 94 ACTIVITES PRINCIPALES Assurer la promotion technique et la vente des produits et des services conformément aux objectifs de vente qui lui ont été déclinés en respectant la politique commerciale et tarifaire de l’entreprise Mettre en oeuvre la stratégie commerciale au niveau sectoriel appliquer les conditions commerciales et négocier les contrats Assurer le suivi des clients, établir et transmettre des rapports d’activité, comptes rendus de visite, renseigner, maintenir à jour et utiliser les outils de la CRM dans le cadre de son activité Utiliser les moyens mis à sa disposition...

The Associate Director in Digital Manufacturing Operations at West Point, PA is a lead for the manufacturing automation team supporting manufacturing of our vaccine products. This position will direct and prioritize workload activities of a professional staff of 5-10 engineers to provide process automation support to enable a reliable and compliant supply of vaccines. The responsibilities include the resolution of automation problems, implementation of process control, data collection and analysis, and troubleshooting in compliance with System Development Life Cycle (SDLC), GMP, safety, and environmental regulations. The successful candidate will have the opportunity to apply their passion, technical skills, and leadership...

Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company—one that is ready to help create a healthier future for all of us. Our company Production Systems (MPS) is an integrated production system for how we design, manage, and continuously improve our operations and supporting business processes, enabled through the development of our people. The Manufacturing Division MPS Team is responsible for driving MPS throughout the organization to enable change in the operating systems, management systems, and mindsets, behaviors and...

Our company is currently seeking an exceptional individual for a technical leadership position within the Supply Analytical Sciences (SAS) - Analytical Chemistry in Development and Supply (ACDS) organization located at Rahway, NJ. The successful candidate will be joining a group of innovative scientists with a focus on drug substance (API) analytical deliverables to drive lead-time reduction and efficiency gains in support of our company’s World Class Supplier and Operationalizing Quality goals. The Senior Scientist position is a laboratory-based scientific track role in a fast-paced, multidisciplinary team environment. The incumbent will be expected to influence external sites in our Company’s world-wide...

Wij zijn op zoek naar een inspirerende leider die zowel aandacht heeft voor menselijk gedrag als voor het behalen van resultaten. Jij hebt de vaardigheid om mensen te ontwikkelen met een competentiegerichte aanpak en begeleidt de professionalisering en prestaties van ons productieteam met een pragmatische stijl die gericht is op continue verbetering. In onze snelgroeiende productieomgeving weet jij het hoofd koel te houden en zorg je voor optimale prestaties. Sluit je bij ons aan als Operational Coach - De Bilt Welkom in ons team Onze productielocatie in De Bilt maakt deel uit van de Animal Health-divisie, waar we vaccins voor...

The Legal Operations, Innovation & Technology team’s responsibilities include financial management, program law firm management, legal records and information management, legal technology strategy, learning and development initiatives, and increasing overall operational effectiveness. We are seeking a dynamic and experienced Associate Director of Outside Counsel and Vendor Management to join our Legal Operations team. In this role, you will be responsible for overseeing the effective management of outside counsel and legal vendors, ensuring alignment with our strategic goals, and optimizing performance and costs. The ideal candidate will have a strong background in legal operations, vendor management, and a deep understanding of...

Les activités de la fonction incluent, mais ne se limitent pas à ACTIVITES PRINCIPALES Assurer la promotion technique et la vente des produits et des services conformément aux objectifs de vente qui lui ont été déclinés en respectant la politique commerciale et tarifaire de l’entreprise Mettre en oeuvre la stratégie commerciale au niveau sectoriel appliquer les conditions commerciales et négocier les contrats Assurer le suivi des clients, établir et transmettre des rapports d’activité, comptes rendus de visite, renseigner, maintenir à jour et utiliser les outils de la CRM dans le cadre de son activité Utiliser les moyens mis...

As a Senior Engineer in Device Design and Process Development group, you will be part of our Research & Development team that designs and develops benchtop/low-volume to high-volume clinical and commercial assembly equipment and processes for medical devices/drug delivery systems. Reporting to the Director responsible for this area, you will partake in medical device assembly and process development using semi-automated and automated equipment, conduct functional testing, assist in clinical batch manufacture as an equipment subject matter expert, assist with acceptance testing (FAT, SAT), installation/qualification of equipment at our manufacturing sites, interrogation of subassembly processes at our device supplier sites, and...

The Technical Operations Director is accountable for the operation of the Technical Operations Department. The role will serve on the Site Leadership Team (SLT) and will be responsible for developing the strategic manufacturing/technical roadmap for the facility. As member of the SLT, the incumbent will play a key role in the development of policy and co-ordination of overall site operations. The role plays a critical part in strategic project realization of the Wilmington Biotech facility, a new hi-potent facility in our company’s Biologic manufacturing network, ensuring that site’s mission and objectives are effectively achieved, consistent with our company's requirements to...

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

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

The Associate Director, Business Insights & Analytics, Cross US Vaccines will be responsible for developing and communicating data-driven and actionable insights that drive greater customer and market understanding to inform launch brand strategies, help meet in-line brand growth and commercial objectives. This role will also oversee strategic planning and execution of initiatives related to HHDDA US Vaccines efforts. This role involves organizing regular business reviews to assess project progress and make informed decisions that align with organizational goals This hybrid role requires the individual to be a lead partner to US vaccines marketing teams in a business facing and analytics...

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

Our company seeks to add an Associate Director. Veterinarian Services at our Millsboro, Delaware location. This position will have overall responsibility for oversight and administration of day-to-day operation of the animal facilities as well as for the veterinary care and animal husbandry program at our company's Millsboro Animal Health facilities. This role is highly compliance-driven in accordance with State and Federal regulations as applicable to the humane care and use of animals. Responsibilities also include training and oversight of the animal care staff, serving as a designated reviewer and voting member of the Institutional Animal Care and Use Committee (IACUC),...

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 provides high quality statistical programming analysis and reporting deliverables for global PK modeling and simulation stakeholders spanning all therapeutic areas. The senior programmer will gather and interpret user requirements, retrieve the required data, transform the data into modeling-ready analysis datasets,...

Our Marketing team is passionate about bringing our medicines and vaccines to our patients around the world. Through digital marketing and engagement analytics, we are able to understand our patients’ and customers’ needs and strive to provide solutions to meet them. A key member of the U.S. Oncology Marketing team, the Patient Channel Strategist will be responsible for defining the media strategies, approving the tactical plans and aligning on the performance measurement for all supported Oncology assets. They will work hand-in-hand with internal and external media, creative and analytic partners to ensure all promotional efforts align with Brand priorities and...

Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety First, Quality Always, Inclusion for All” mindset striving for continuous improvement. We work in the local plant connected to our global manufacturing network to ensure the highest quality of raw materials, intermediates and finished products. The Specialist Manufacturing Automation in the West Point Digital Manufacturing Operations organization will be responsible for supporting process automation systems in manufacturing. The candidate will provide day to day support functions working closely with partners in operations, engineering, maintenance, and quality. General responsibilities include Troubleshooting...

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

We are seeking an exceptional computational protein engineer to join the Discovery Biologics Protein Engineering department in South San Francisco to drive the advancement and application of computational antibody and protein designs and optimization in support of our biotherapeutic portfolio drug discovery programs. The Principal Scientist, Computational Protein Engineering role will be a key contributor within the Protein Engineering Center of Excellence and the Discovery Biologics department as well as in project teams and therapy areas. We are on a quest for cures and are committed to be the world’s premier, most research-intensive biopharmaceutical company. Our teams combine leading drug...

As part of Our Company’s Manufacturing Division, within the Vaccine Science and Technology (VS&T) organization, the Vaccine Drug Substance Commercialization (VDSC) Downstream Process department provides the technical process leadership and laboratory capabilities in support of late-stage pipeline and commercial manufacturing purification processes for vaccines. VDSC supports a combination of commercialization activities for pipeline and commercial program support, including process development and characterization laboratory experiment design and execution, technology transfer to internal and external manufacturing sites, process validation, manufacturing investigations and trend analysis, process enhancements, next generation process development, and authoring of regulatory submissions. Under the general scientific and administrative department...

The Site Analytical Science team within Global Quality- Large Molecule Analytical Sciences (GQ-LMAS) team provides support of late-stage pipeline programs through commercialization and launch as well as product lifecycle management support. The position will work closely with partners with Large Molecule Analytical Science (GQLMAS), Sterile Quality Assurance Center of Excellence, Technical Operations, Operations and our manufacturing division Quality to provide site microbiology support. The successful candidate will have the opportunity to apply his or her enthusiasm and microbiological skills in the operation and improvement of a manufacturing facility. This role requires the ability to manage multiple complex projects, activities, and/or...

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity, and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, inclusion, and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. 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....

The Utilities Electrical Engineering Lead is a member of the Plant Engineering team providing technical support to the Durham Site. The site includes an Energy Center, Vaccines DP and DS Manufacturing Facilities, Quality Labs, various other manufacturing buildings and Maintenance and Material Storage Facility (MMSF). This support position will focus on leading investigation of Electrical system excursions, engineering maintenance, design system improvements and optimizations. This individual will provide input to the deviation investigation process for determination of root cause, recommend corrective actions to prevent re-occurrence and help assess the impact on operations. The incumbent will also be responsible for leading...

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

This position will be part of the Device Quality & Regulatory Team within Global Regulatory Affairs and Clinical Safety (GRACS). The primary responsibility for this position is to ensure regulatory compliance for the company's portfolio of medical devices and medical device combination products. Primary activities include, but are not limited to Serve as coordinator for management review of the company's device quality management system, including working with sites to collect, analyze and summarize data for management review meetings and presentations. Support device related internal, notified body and health authority inspections Provide support for quality system initiatives by generating, managing, and...