Merck Job Trends

Global Clinical Data Standards Therapeutic Area Lead At Join our team and contribute to our mission of making a difference in global health. Responsibilities Define standard collection and mapping data definitions, ensuring alignment with industry (CDISC) standards and Health Authority regulations. Ensure the definitions are maintained and aligned across the clinical lifecycle (e.g., data collection, analysis & report, and submission) deliverables. Lead standards data governance reviews. Contribute to the definition and maintenance of business processes related to the definition, use, maintenance, and sharing of clinical data standards. Lead or participate in department initiatives, cross-functional working groups, and process improvement...

The Vaccine Key Customer Leader (VKCL) is the primary our company vaccines point of contact for strategically assigned key private and public sector customers within a designated market. The VKCL leads vaccine growth strategy for the assigned ecosystem(s), key accounts, engages C‑/D‑suite, senior clinical and operational leaders, and drives measurable business performance and customer experience. The role coordinates cross‑functional our company teams (field and HQ) to ensure implementation and pull‑through at clinic/health system/provider level while proactively identifying growth opportunities and compliant solutions to competitive threats. This is a field-based account management role that is responsible for covering the following states...

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

Biologics Process Research & Development (BPR&D) within our Company's Research Laboratories is on a mission to rapidly deliver biotherapeutics to patients by efficiently developing innovative, robust manufacturing processes and technologies. To achieve this, we work closely with colleagues in Discovery, Pre-clinical, Early Development, Analytical, Formulation, and Commercial Manufacturing while providing an inclusive environment for all. Beyond process development for pipeline biologics, we innovate and build next generation biomanufacturing technologies. Examples include investments for development of continuous manufacturing, green and sustainable processes, and proprietary technology platforms. We actively publish and engage with the scientific community to influence the field. Biologics Process...

Global Clinical Trial Operations (GCTO) is a global organization with over 9500 people operating in 47 countries. The Clinical Sciences and Study Management organization (CSSM) is a sub-functional unit within GCTO, divided into three therapeutic clusters, with over 1000 people, and is accountable for all operational, technical, and scientific aspects of HQ-sponsored clinical trials, including a grant budget more than $1B. Key activities for this role include the strategic planning, oversight, management and execution of HQ-sponsored trials for the assigned Therapeutic Area Section, including local registration trials and regulatory commitments. The position is also directly responsible for the technical/ scientific...

The Biologics & Biopharmaceutics team is an integrated team responsible for the development and successful registration of new drug products. Formulation activities focus on the development of non-oral dosage forms spanning preclinical toxicology studies through commercialization. We ensure robust composition, primary packaging/device, and process selection through deep fundamental understanding and characterization such that the process is scalable without compromising stability, safety, efficacy, and delivery. Biopharmaceutics scientists proactively develop and execute a comprehensive biopharmaceutics strategy that leverages cutting edge in vitro, in vivo and in silico Physiologically Based Pharmacokinetics (PBPK) and PK modeling tools, while advancing the underlying biopharmaceutics science within...

Biologics Process Research & Development (BPR&D) within our Company's Research Laboratories is on a mission to rapidly deliver biotherapeutics to patients by efficiently developing innovative, robust manufacturing processes and technologies. To achieve this, we work closely with colleagues in Discovery, Pre-clinical, Early Development, Analytical, Formulation, and Commercial Manufacturing while providing an inclusive environment for all. Beyond process development for pipeline biologics, we innovate and build next generation biomanufacturing technologies. Examples include investments for development of continuous manufacturing, green and sustainable processes, and proprietary technology platforms. We actively publish and engage with the scientific community to influence the field. Biologics Process...

We are seeking a highly motivated Specialist of Financial Data & Analytics to work on the development and delivery of advanced analytic solutions that support strategic decision‑making across the enterprise. This position will partner closely with divisional SMEs—including HH Finance, Manufacturing Division Finance, Research and Development Division Finance, Corp Finance, Tax and Treasury—to define solution requirements. The Specialist will develop solutions based on designs provided by the larger project team. This role requires strong problem-solving skills and developing technical know-how. Also working effectively with business and technical team members will be critical. Primary Responsibilities Analytics Solution Design & Delivery Document...

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

Our US Ophthalmology team is committed to transforming the lives of patients living with diabetic macular edema (DME) and neovascular age-related macular degeneration (nAMD) with a portfolio of two products in the pipeline. We aspire to achieve this through a relentless commitment to patients, innovation, ensuring access to life‑changing therapies, and collaborating with healthcare systems, governments, and payers to make treatments available to those who need them most. Our focus is on patients, scientific rigor, and flawless execution—bringing breakthrough therapies to those who need them. We are seeking an experienced Associate Director of Ophthalmic Learning & Development to lead the...

Biologics Process Research & Development (BPR&D) within our Company's Research Laboratories is on a mission to rapidly deliver biotherapeutics to patients by efficiently developing innovative, robust manufacturing processes and technologies. To achieve this, we work closely with colleagues in Discovery, Pre-clinical, Early Development, Analytical, Formulation, and Commercial Manufacturing while providing an inclusive environment for all. Beyond process development for pipeline biologics, we innovate and build next generation biomanufacturing technologies. Examples include investments for development of continuous manufacturing, green and sustainable processes, and proprietary technology platforms. We actively publish and engage with the scientific community to influence the field. Biologics Process...

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

Support domestic and international tax planning initiatives within the Tax Organization, including (i) performing technical analysis, (ii) preparing tax planning presentations, (iii) modeling the tax impacts and supporting the implementation of tax planning initiatives, (iv) drafting intercompany agreements, and (v) working with tax operations on the accounting and reporting implications of tax planning initiatives. Considering the strategic relevance of business development structuring and supporting business development transactions will be your main area of focus. Tax Organization liaison with (i) Business Development; (ii) Accounting, and (iii) Finance, each as further described below. Business Development (i) Manage tax due diligence related...

The Biologics Analytical Research & Development department of our Company's Research Laboratories Division is seeking applicants for a Principal Scientist position available at its Rahway, New Jersey research facility. The Principal Scientist is a highly visible and impactful senior scientific role tasked with working closely with the group Director to define analytical strategy and to lead a team of scientists in solving complex analytical problems at the interface of biology, chemistry, and lab informatics disciplines to enable development of biologics active pharmaceutical ingredients (APIs). We are looking for a team player with strong leadership skills and the passion for mentoring...

Overview The Director, Global Media Relations, is a highly proactive communications leader responsible for shaping and executing a global media strategy that elevates This leader is highly knowledgeable of Our Company's science, products, and pipeline, and possesses an understanding of biology and high-level scientific concepts and approaches, clinical research and drug discovery and development. Furthermore, this leader is dedicated to understanding the intricacies of each business area to enable the accurate and effective external positioning of Our Company's corporate story. This leader is self-motivated, detail oriented and maintains strong project management skills. This individual also can develop and execute...

Position Overview Associate Director, Companion Animal Marketing, Parasiticides will support and drive commercial growth for our parasiticide portfolio in the United States, partnering across Brand, Digital, Field Sales, Commercial Operations and external agencies. The Associate Director Parasiticides role requires deep direct-to-consumer (DTC) marketing capabilities with broad multi‑channel commercial experience (veterinary channel, distribution, e-commerce and retail) and people leadership responsibilities. The reports to the Director, Parasiticides Marketing and will be an integral member of the brand and cross‑functional teams. At our company's Animal Health, you’ll join a team that’s passionate about the human–animal bond and committed to caring for animals across...

Collaborate with stakeholders to gather and translate business requirements into technical specifications and product features. Monitor and enhance adoption and usage of the product and digital services. Work closely with the cross organizational teams to develop integration points that streamline business processes. Research and evaluate emerging technologies (e.g., AI, machine learning, blockchain, IoT) to identify opportunities for innovation within the integration platform. Lead cross-functional global agile teams implementing platforms or solutions. Develop and execute the integration strategy across health sciences orgs and systems like SAP ERP, ensuring alignment with business goals. Identify integration requirements and drive the implementation of solutions...

The Vaccines Analytical Research and Development (Vaccines AR&D) team within the Large Molecule Analytical department is seeking applicants for a lab based, Scientist position at its West Point, Pennsylvania, research facility. The scientist is a laboratory-based scientific role that establishes and maintains laboratory automation and robotic systems used to support high-throughput analytical assays. The primary lab-based role of the successful candidate will be to accurately perform automated and robotic biochemical, immunoassay, and cell-based methods. The candidate must be able to independently troubleshoot technical issues, participate in day-to-day lab maintenance activities, maintain accurate records, and be responsible for timely communication of...

Délégué(e) Commercial pour le secteur suivant Départements 49-53-72 Missions - Assurer la promotion des médicaments et solutions auprès des professionnels de la santé animale (vétérinaires et ASV) - Proposer des solutions de développement et assurer la formation médicale dans les structures vétérinaires du secteur - Remonter les informations du terrain, et notamment celles concernant la veille concurrentielle - S'intégrer dans une équipe de 8 délégués, et travailler en collaboration avec son Directeur Régional, son responsable médical terrain et les équipes du siège Required Skills Account Management, Account Management, Adaptability, Animal Handling, Animal Health Care, Data Analysis, Drug Administration,...

This position will be responsible for the leadership, oversight and direction for the regulatory review function of US Office of Promotion and Advertising Review (OPAR) . This role has ad/promo regulatory review accountabilities across all Therapeutic Areas of our company's portfolio in the US. This role will manage a team of reviewers and supporting roles to set the strategic direction for a staff of 30+ professionals. This executive leadership position has Strategic Responsibilities Regulatory Guidance Interpret and apply advertising and promotion regulations in reviews. Proactively design risk mitigation that anticipates the evolving regulatory landscape and allows for aggressive yet...

Join us and experience our culture first-hand one of strong ethics & integrity, diversified experiences, exceptional science, and a resounding passion for improving human health. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. In your role as Associate Principal Scientist, you will be a critical part of the Analytical Research and Development Microbiology team with responsibilities including leading the rapidly growing pipeline via collaboration with stakeholders to deliver on critical data in a good manufacturing practices (GMP) microbiology laboratory including finished products testing, utilities,...

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

We are seeking a motivated Automation Scientist to join our Quantitative Biosciences team in Boston with a primary focus on sample management. The successful candidate will manage sample workflows and ensure the integrity, traceability, and timely processing of samples used in analytical and bioanalytical assays. This role requires hands-on experience with automated liquid handling platforms and sample management workstations. Key Responsibilities Operate, maintain, and troubleshoot automated sample handling equipment, including Hamilton liquid handlers, Echo acoustic dispensers, Access Workstations or like devices. Execute daily sample processing workflows (plate preparation, aliquoting, reformatting, inventory tracking) to support assay and study timelines. Coordinate sample...

In our Company's Research Labs, we identify and target steps in disease mechanisms or pathways that could be inhibited or enhanced. Our goal is to isolate a compound that is effective against a disease target. Using innovative thinking, state-of-the-art facilities and robust scientific methodology, we collaborate to discover the next medical breakthrough. Seeking candidates for a unique and exciting opportunity to bridge across two pilot scale facilities in VAX and Biologics Process Research and Development. The Vaccines and Advanced Biotechnologies Process Research & Development (VAXPR&D) and Biologics Process Research & Development organizations within our Company Research Labs are broadly responsible...

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. The Regional Medical Scientific Director's liaise between the scientific community and the Company to enhance the comprehension of scientific foundations and goals...

Position This position is part of the COSI (Cost of Sales & Inventory) organization, which performs end-to-end activities of accounting for units of inventory all through the supply chain. In this role the Senior Specialist will be responsible for maintaining, reviewing, reporting and analyzing inventory, intercompany profit, production and product cost data, in supporting the monthly accounting close and management cycles for one or multiple plants. This role is responsible for the following Maintain and create product cost according to US GAAP rules. Control, analyze and report production results and source-to-settle variances monthly to business partners by providing high-level...

The Analytical Enabling Capabilities organization in West Point, PA is seeking a motivated scientist with technical expertise in mass spectrometry-based protein, protein conjugation or oligonucleotides or polysaccharide characterization. In addition to mass spectrometry skills, we are also seeking candidates with strong proteomics and data science skills. The successful candidate is expected to independently conduct mass spectrometry experiments to support multiple vaccines programs, represent the team in cross-functional teams and develop new methods to solve current industry challenges. The work requires documenting experiments in electronic laboratory notebooks, authoring summaries to inform stakeholders, as well as presenting at seminars and publishing in...

We are seeking a Data Scientist to join our R&D Quality Assurance Analytics & Tech Systems team. This role will be both responsible for developing and maintaining innovative data science solutions, and developing our Analytics solutions. The successful candidate will work closely with our business stakeholders to determine areas for business growth, develop new solutions using innovative technology, such as machine learning and generative AI, and develop/maintain Analytics Tools. Key Responsibilities Technically support current and new Data Science requests within our Research & Development Division QA space, including developing new innovative models and maintaining current solutions. Develop and support...

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 studies 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 the V&I, Outcomes Research teams in Lung Cancers. Primary Responsibilities This position has primary responsibility for planning/managing a comprehensive program of real-world evidence and non-interventional research activities for in-line and pipeline products for lung cancers to meet the value evidence needs of clinicians, payers, policymakers, health technology assessment (HTA)/reimbursement agencies, and...

We are seeking a dynamic Learning Partner to lead our Immunology Learning and Development team and play a pivotal role in preparing our commercial organization for a successful product launch. In this role you will deliver innovative, evidence-based learning experiences that translate clinical information for our customer-facing teams. You will partner closely with Marketing, Sales Leadership, Market Access and Field Facing teams to assess capability gaps, build targeted curricula, and measure learning impact—ensuring our launch readiness is aligned with strategy, compliance, and patient-centered outcomes. The ideal candidate combines deep scientific understanding of immunology with adult-learning expertise, customer facing/pharma sales experience,...

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

The Sterile Product Development (SPD) group is responsible for developing non-oral dosage forms (injections, implants, inhaled, ocular) for small, intermediate, and large molecules from preclinical toxicology studies to commercialization. Our development teams ensure robust composition, primary packaging/device, and process selection through deep fundamental understanding and characterization such that the process is scalable without compromising stability, safety, efficacy, and delivery. During development, we leverage smart experimental design, cutting edge analytical tools, and predictive approaches to inform molecule, formulation and process selection. In summary, our team enables the translation of preclinical candidates into non-oral drug products. Our team is looking for a...

Senior Specialist, Metrology and Validation, Pharmaceutical Analysis & Digital Technologies The Pharmaceutical Analysis & Digital Technologies (PADT) External Capabilities, Validation, and Compliance (ECVC) department of our company's Research Laboratories Division is seeking applicants for an Metrology and Validation Specialist position available at the West Point, Pennsylvania research facility. The Metrology and Validation Specialist will work as part of the integrated US Metrology and Validation team and drive a culture of quality and operational excellence across the global Development Sciences & Clinical Supply (DSCS) network. The role oversees and supports the onboarding, qualification, validation, and routine maintenance of analytical equipment...

ROLE OVERVIEW The Associate Director, Portfolio Management is a key leadership role within our company's Finance Digital Office, responsible for governing and advancing the FDO's portfolio of digital transformation initiatives across a global finance organization of over 1,000 employees. This individual will serve as the connective tissue between strategic intent and execution; ensuring that projects are prioritized, resourced, tracked, and communicated with rigor and transparency. This role requires a rare combination of financial acumen, project management discipline, and digital fluency. The successful candidate will build and maintain the frameworks, tools, and governance processes that enable the FDO to deliver value...

The Office of General Counsel is seeking an experienced Patent Docket Specialist to provide operational support to the Intellectual Property (IP) organization. Primary responsibility is to ensure all patent prosecution activities are accurately and timely entered into the docketing system in accordance with U.S. and international patent law and procedure. This position has a flexible hybrid office schedule based in Rahway, NJ. A successful candidate should possess strong oral and written communication skills, be self-motivated and excel in a team environment. The candidate should also have a demonstrated capacity to manage and prioritize multiple tasks efficiently in a high-volume environment...

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

The Materials & Biophysical Characterization (MBC) group within Analytical Research & Development is seeking a highly motivated and technically focused individual interested in positively impacting our Company's pipeline from discovery through development and commercial launch. This position is for a Pharmaceutical Materials Scientist to be a key member of a team responsible for the physicochemical characterization of pharmaceutical materials including small molecule active pharmaceutical ingredients (API), chemical intermediates, peptides, novel excipients, drug-product intermediates, and drug products. The candidate will utilize their expertise in physical organic chemistry or materials science as a member of cross-functional teams to tackle scientific challenges related...

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

The role of Director, Global Communications, Oncology is a unique opportunity to join our company, a recognized leader in oncology, as a key member of the Global Oncology Communications team. The role is dedicated to managing day-to-day communications related to our company’s broad oncology portfolio and pipeline assets. The candidate selected for this role will work under the guidance of the Executive Director, Global Oncology Communications, in a fast-paced and ever-changing environment. Responsibilities include but will not be limited to the following key activities Lead communications activities in support of our company’s oncology in-line products and Phase 3 pipeline assets;...

This role is accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, our company policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight of the Sr. COM, Head COMs or CRD, the person is responsible for preparing, analyzing, negotiating, and revising Clinical Research related contracts and budgets through all phases of the contract cycle. Responsibilities include, but are not limited to Prepare, analyze, negotiate, and execute required site agreements and associated budgets including Clinical Trial Research Agreements (CTRA), Master Clinical Trial Research Agreements (MCTRA),...

Role Summary The U.S. Director of Medical Affairs (US DMA), COPD, position resides in the Value & Implementation (V&I) organization, which includes Global Medical and Scientific Affairs as Outcomes Research. The US DMA is a regionally based position within U.S. Medical Affairs (USMA). This position strategically drives scientific excellence across in-line business and the One of our company's Pipeline while optimizing field readiness across the USMA strategic pillars 1) Scientific Exchange; 2) Company Trials; 3) Investigator-Sponsored Programs; 4) Congresses; and 5) Scientific Insights. The US DMA is an experienced therapeutic area (TA) leader and subject-matter expert (SME) with relevant medical...

ROLE OVERVIEW The Associate Director, Community Engagement is a dynamic and people-centered leadership role within our company's Finance Digital Office, responsible for building, activating, and sustaining a thriving digital community across a global finance organization of over 1,000 employees. This individual will design and lead engagement programs that connect finance professionals around shared learning, digital adoption, and emerging technology; creating the community infrastructure through which the FDO's transformation agenda comes to life. The ideal candidate is an energetic connector and communicator who brings finance domain knowledge, a talent for program design, and a genuine passion for bringing people together around...

We are seeking a highly experienced and skilled Senior Glass and Critical Component Technical Expert to join our team as a key technical support resource for our pharmaceutical and combination product engineering projects. The ideal candidate will have extensive knowledge and expertise in the design, development, and manufacturing of glass components such as syringes and vials for pharmaceutical and combination product applications. Position title Associate Principal Scientist — Glass & Critical Components Location West Point, PA or Rahway, NJ (Hybrid). Travel up to 15–25% as needed. Reporting Reports to Distinguished Scientist, Glass & Critical Components Role summary The Associate Principal...

We are seeking a highly motivated and experienced Senior Specialist of Financial Data & Analytics to work on the development and delivery of advanced analytic solutions that support strategic decision‑making across the enterprise. This position will partner closely with divisional SMEs—including Human Health Finance, Manufacturing Division Finance, Research and Development Division Finance, Corp Finance, Tax and Treasury—to define solution requirements. The Senior Specialist will develop solutions based on designs provided by the larger project team. This role requires strong business acumen/knowledge, problem-solving skills and technical know-how. Also working effectively with business and technical team members will be critical. Primary Responsibilities...

Supports IT Risk Management & Security product and project leads by managing financial planning, forecasting, accruals, and compliance activities. Partners with stakeholders to track budgets, forecasts, and actuals, ensure financial governance adherence, drive timely delivery of financial commitments, and provide actionable financial insights to support informed investment decisions. This role is ideal for a candidate with a strong foundation in financial coordination who aspires to grow into a Project Manager or Scrum Master role. What will you do in this role Support product and project leads in the development and management of financial, spend, and accounting plans Obtain, document, and...

The Customer Segment Strategy team within Integrated Account Management (IAM) Strategic Insights is responsible for developing US market access strategies for key customer segments to enable success across our portfolio. We focus on customer segments that are critical to unlocking patient access now and in the future, including Specialty Pharmacies, Specialty GPOs, and Payers/PBMs. As an Associate Director, US Market Access – Specialty Pharmacy Strategy , you will be responsible for the Specialty Pharmacy (SP) Customer Segment , with strong connectivity to Payer/PBM and Specialty GPO/distributor dynamics as they impact the patient journey and access. You will serve as a...

T ranslational Med icine ( TMed ) drives early clinical development of novel therapeutics by partnering with Discovery Sciences and Late-Stage Clinical Research to translate scientific discoveries into human proof-of-concept and advanc e the most promising candidates through the pipeline to patients . We design and execute clinical pharmacology strategies spanning first-in-human studies through proof - of -biology/ proof-of- concept and into late-stage development , supporting worldwide marketing applications and lifecycle management . In a competitive external landscape and fast-pa ced internal environment , t h is position provide s both strategic and operation al leadership across early immunology programs...

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

The Vice President, Global Medical and Scientific Affairs (GMSA), Therapy Areas builds and develops teams accountable for Therapy Area (TA) leadership, strategic planning, and execution for therapy areas globally. Their teams cover all therapy areas in their portfolio. As member of the Company Research Laboratories Global Medical and Scientific Affairs (Research & Development (R&D) GMSA) Leadership Team they partner with other R&D GMSA leaders to maximize all medical and scientific activities are aligned with R&D GMSA’s priorities and demonstrably address opportunities/challenges in countries and regions. The Vice President (VP) partners with the Research Leadership Team, commercial Customer Business Lines/ Global...

As a Assoc Principal scientist, you will drive the creation of next-generation mammalian cell lines using a systems-level approach . You will be responsible for designing synthetic genetic circuits, managing large-scale multi-omics datasets, and utilizing Next-Generation Sequencing (NGS) to ensure the stability and productivity of therapeutic cell lines. Key Responsibilities Cell Engineering & Synthetic Biology Design and optimize complex DNA vector constructs and synthetic gene circuits to enhance protein expression in CHO cells. Use cutting -edge gene-editing tools for targeted knock-in/out strategies. Systems Biology Integration Develop and apply computational models to understand cellular pathways and metabolism, predicting how...

Applications are sought for an SAP Master Data Sr. Specialist in Vaccines and Advanced Biotechnologies Process R&D (VAX PR&D). The role supports pilot-scale GMP manufacture of bulk biologic clinical supplies (vaccines and therapeutic proteins) and will create, design, and sustain standardized business processes, master data governance, system sustainment, and lifecycle material management, while providing peer coaching and expert consultation. The position will be temporarily based in West Point, PA for approximately 18 months (up to 24 months) to support business needs. After this period, the role is intended to relocate to Rahway, NJ. Applicants should be comfortable with this planned...

The US Director of Medical Affairs (DMA) for Gynecologic Malignancies (Ovarian, Endometrial and Cervical Cancer) holds primary responsibility for the development and execution of regional oncology Medical Affairs strategies and plans for Gynecological Malignancies in the US across indications. The US DMA for Gynecological Malignancies provides scientific and medical expertise to the US Medical and US Marketing organizations. Primary activities include, but are not limited to Develops and executes US Medical Affairs strategy for Gynecologic malignancies Drives creation and facilitation of training materials for the Oncology Medical Affairs team through the appropriate review systems and serves as the medical...

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. Summary Responsibilities This position provides high quality statistical programming deliverables for global stakeholders in Early Development Statistics and PK/PD Modeling and Simulation spanning all our Company's therapeutic areas except oncology. The senior statistical programmer will gather and interpret user requirements for...

The Contracting and Distribution Strategies team in U.S. Vaccines is seeking a Customer Manager who will be responsible for managing our contracts and agreements in the Public Sector (inclusive of CDC, VA, and DoD segments). This position partners with key internal stakeholders, including Brand Marketing, Portfolio Marketing, Global Market Access & Pricing, Policy, Order Management Center, Manufacturing, CCM, Customer Operations, Commercial Legal, Data and Analytics Teams, Finance, Account Management, and Vaccine sales teams. Key Responsibilities Contracting & Customer Management · Lead the design & execution of CDC contracting including the addition of launch products. · Evaluate and update strategy and...

Welcome to the Future of Precision Oncology – Join Us in Wilmington, DE! We’re thrilled to announce the launch of our cutting-edge Antibody Drug Conjugate (ADC) manufacturing facility in Wilmington, Delaware—a bold step forward in transforming cancer care through innovation, collaboration, and purpose-driven science. This is more than a job - it’s a chance to be part of the next wave of cancer care. Whether you're an engineer, scientist, operator, or quality expert, your work here will contribute to life-changing therapies for patients around the world. Together, we’ll build a facility that not only meets the highest standards of safety...

At Join us in our mission to make a difference. The Biologics VCM Product Leader (PL) is the end‑to‑end supply chain owner for one or more biologics, accountable for defining and executing integrated product supply strategies across the lifecycle. This role oversees supply chain design, global filing and launch planning, long‑range demand and capacity alignment, risk management, cost of goods projections, and post‑approval product, process, and supply chain changes. Through these responsibilities, the VCM PL directly influences cost, quality, customer service, compliance, and ultimately product availability, continuity of supply, and commercial performance. As the leader of the Supply Chain...

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

The role is on-site, based in Rahway, NJ and will support our second shift operations which operate from 300 PM EST to 11PM EST. Join us and experience our culture first-hand one of strong ethics & integrity, diversified experiences, exceptional science, and a resounding passion for improving human health. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. In the role of Associate Principal Scientist, you will be a key member of the Analytical Research and Development Microbiology team, supporting a rapidly expanding pipeline through...

The Maintenance/Utility Lead is an Associate Director that is accountable for the management of all maintenance staff supporting Infrastructure Maintenance, Vaccine, and Biologic or Antibiotic Sterile operations. This group is responsible for improving asset reliability and manufacturing capacity by providing maintenance and technical support in the field in compliance with Good Manufacturing Practice (GMP), Safety, and Environmental regulations. Education Minimum Requirement High School Diploma/GED and a minimum of fifteen (15) years of experience in Manufacturing, Maintenance or Military environments OR Associate’s Degree in Engineering (Mechanical, Chemical, or similar discipline) or related scientific field (Chemistry, Physics, Math) and a minimum of...

Associate Director, Integrated Facilities Management Description The Associate Director, Integrated Facilities Management, will be responsible for providing guidance, oversight, and management of the Integrated Facility Management (IFM) program at the Elkton, VA site. He/she will work with cross-functional teams to effectively and safely operate and maintain designated buildings, site infrastructure and systems to support various site functions at a competitive cost. This role will be a highly-collaborative role with customers in EH&S, Operations, Engineering, Procurement, Finance, and other global partner groups to drive compliance with the IFM contractual Service Level Agreements (SLA’s) and Key Performance Indicators (KPI’s). The essential functions...

The Discovery Analytical Research group in West Point, Pennsylvania is seeking application for an Associate Principal Scientist position to drive innovation in analytical measurement technologies, enabling the discovery of new drug candidates across diverse modalities. Key deliverables will include the development, implementation, and execution of analytical measurement technologies that accelerate the pace of discovery research and influence molecular design. The successful candidate must be able to collaborate in a dynamic, integrated, and multidisciplinary team environment. A broad range of tools (e.g. high-resolution mass spectrometry, chromatography, spectroscopy) are leveraged, and new technologies are developed to influence selection of new drug candidates...

Senior Scientist, Regulatory CMC Biologics Position Serve as a Regulatory CMC Project Lead and provide CMC Regulatory leadership within Regulatory and on cross-functional teams for the assigned biological projects. Be accountable for the delivery of all regulatory milestones through product development and / or post approval life cycle. Ensure development of robust CMC regulatory strategies for assigned projects. Be accountable for the execution of global product regulatory strategy(ies) by robust assessment of global regulatory CMC requirements and identification of potential risks. Manage execution of CMC documentation including IND/IMPD, original BLA/MAA, or Post approval / variations, agency background packages and...

Scientist (R2) Bioassay North American GMP Operations, Rahway, NJ We invite individuals who possess a deep passion for promoting lifesaving and life-enhancing products to join our dynamic team. Our team is highly dedicated and committed to offering exceptional scientific oversight, driving the success of our Company’s extensive range of products from candidate selection to market authorization. At our company, we proudly continue to build upon a legacy of groundbreaking innovation while steadfastly upholding the highest standards of ethics and integrity. With a diverse workforce representing a multitude of languages and cultures, we stand unified in our collective mission to deliver...

We are seeking an innovative and experienced scientist to join the Discovery Biologics Protein Engineering department in South San Francisco to lead both functional area scientists and drug discovery programs. The Principal Scientist, Protein Engineering role carries leadership responsibilities as a functional SME and project team lead interfacing with multiple cross-site groups within the Discovery Biologics department and therapeutic areas. We recognize that in our team is our strength and are committed to creating an inclusive environment for all employees. Successful candidates must demonstrate inclusive behaviors in working with a group of scientists to drive our core mission. What you...

At our company's manufacturing facility in Elkton, Virginia, we currently have a Maintenance Manager position available at the Elkton Campus; which is located in the Shenandoah Valley along the Shenandoah River and the Blue Ridge Mountains. The facility is a short distance from major state universities University of Virginia and James Madison University. The Maintenance Manager will work with the maintenance manager to coordinate all maintenance activities and manage the associated union hourly workforce to ensure attainment of business results on their respective shift. The Maintenance Manager will act as the maintenance manager during periods of absence. The incumbent will...

The function of Senior Specialist, Engineering at Bio Technology and Solutions (BTS) - Tech Hub will have a focus in Vaccine and Biologicals processes development for Manufacturing. BTS Tech Hub is responsible for process development of production processes. Within a multidisciplinary environment you will cooperate with your colleagues at BTS, Manufacturing, Engineering, Quality and R&D. Your main field of attention is to provide all round technological support on Vaccine and Biologicals Manufacturing of new (R&D) products. Primary Responsibilities Leads and works independently as a team member on the development and scale up of processes or technologies of microbial, virus and...

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. We have an exciting opportunity for an Associate Specialist to join the Continuous Improvement team for a capital project start-up in Durham, North Carolina. The facility includes end-to-end processing of drug substance, drug product, including biotech culture growth, harvest, lyophilization, product inspection, and quality control laboratories. This position...

The Pharmaceutical Analytical Sciences group has an opening for a second shift Specialist based in Rahway, NJ. Join us and experience our culture first-hand - one of strong ethics & integrity, diversified experiences, exceptional science, and a resounding passion for improving human health through innovative drug delivery technologies and predictive analytical tools. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. In your role as Specialist, you will be part of a team in charge of managing, coordinating, and facilitating analytical support for the Rahway...

Position Overview - Basic Functions & Responsibility Essential function{s) includes, but is not limited to Reporting to the Associate Director of PTO Engineering, the Senior Process/Project Engineer is responsible for providing technical support of our Manufacturing Division-Wilson packaging and medical device assembly lines. Responsible for specifying, purchasing, installing, and qualifying new packaging and device assembly equipment. Also responsible for packaging and device assembly equipment performance, support, and troubleshooting for products packaged at our Manufacturing Division-Wilson. Works closely with Wilson and above-site departments for the transfer of new products and processes from our Research & Development Division or other Manufacturing Division...

The Director, Global Market Access – RSV leads the development and integration of global market access, pricing, and reimbursement strategy for the RSV portfolio across launch and lifecycle. This role will serve as Global Access Lead and is accountable for shaping payer value, guiding evidence and policy strategy, and enabling successful access outcomes across regions and countries. The Director collaborates closely with global, regional, and country teams to drive strategic alignment, develop payer value resources, and influence clinical, economic, and evidence generation plans. The role leads cross‑functional workstreams and is accountable for identifying, assessing, and proactively shaping access risks, opportunities,...

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

Small Molecule Analytical Research and Development (SMARD) is seeking a highly motivated Associate Principal -Microbiologist to join the growing Microbiology Center of Excellence (COE). Based our company's Headquarters in Rahway NJ, this position is responsible for supporting the full company Portfolio which includes small molecule, biologics and vaccines. As a main contributor to the implementation of new technologies and alternate microbiological methods, and – with the adequate background - The individual interacts with internal and external partners to foster collaborations and actively contributes to the establishment of our Research & Development division Micro CoE. Responsibilities include supporting the rapidly growing...

The Analytical Research and Development Microbiology group has an opening for a Scientist - Microbiologist. Join us and experience our culture first-hand one of strong ethics & integrity, diversified experiences, exceptional science, and a resounding passion for improving human health. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. In your role as Scientist, you will be a critical part of the Analytical Research and Development Microbiology team with responsibilities including leading the rapidly growing pipeline via collaboration with stakeholders to deliver on critical data...

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

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

Advertising Senior Specialist This role is responsible to lead the Decideware platform enterprise wide and support the sourcing of creative agency services, within Marketing Procurement supporting the total category spend of $450M. This role reports to the Associate Director of Procurement for Creative Agencies. The candidate will support the re-development of the Decideware platform and the procurement requirements to implement the tool globally. This will include platform strategy, global category management, surveys, scope shells, rate card management, risk management, stakeholder management, and supplier value management within the creatives category. Primary activities include but not limited to Support category management and...

The Future Talent Program features Cooperative (Co-op) education that lasts up to 6 months and will include one or more projects. These opportunities in our Research and Development Division can provide you with great development and a chance to see if we are the right company for your long-term goals. Role Overview The co-op will support development of translational in vitro models relevant to different therapeutic areas with an emphasis on iPSC-derived systems and assay execution. This role offers hands-on laboratory experience, exposure to cross-functional project teams, and opportunities to communicate results. Responsibilities · Support routine maintenance of cell-based systems...

Our Company has an exciting and growing Immunology pipeline, reinforcing our position as a sustainable innovation engine for the coming decade as we aspire to become the trusted leader in delivering novel solutions to transform the standard of care for Immune-Mediated Diseases. The Immunology portfolio is a top corporate priority for our company and will be a key growth driver for our company. Our Global Market Access (GMAx) organization is driven by a passion to save and improve lives through ensuring sustainable access to our medicines and vaccines at a price reflective of their value. We work collaboratively across the...

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

The Data, AI & Genome Sciences department is looking for a passionate and talented computational biologist with deep expertise in image analysis to join our Translational Genome Analytics research team. In this role, you will apply AI/ML-based analytics to analyze large multi-scale and multi-omics imaging- and functional genomics-based datasets and closely collaborate with a cross-functional team of computational biologists, data scientists, and stakeholders in Discovery Research to drive target and biomarker discovery and drug development efforts. This role will support multiple therapeutic areas with a strong emphasis on Oncology. The successful candidate will be a scientifically curious team player, strong...

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

We are seeking an experienced, detail-oriented Associate Director to join the Biologics Pilot Plant (BPP) Operations team within Vaccines and Advanced Biotechnologies Process Research and Development (VAXPR&D). In this role you will lead, author, document, and drive formal investigations of process deviations, non-conformances, and incidents to determine root causes and ensure compliance with regulatory requirements and internal standards. You will partner closely with process development, manufacturing, and quality colleagues to implement corrective and preventative actions, support investigation governance, and improve operational robustness across upstream and downstream pilot operations. The position will be temporarily based in West Point, PA for approximately...

Associate Director, U.S. Marketing Ophthalmology HCP Field Execution Our US Ophthalmology team is committed to transforming the lives of patients living with diabetic macular edema (DME) and neovascular age-related macular degeneration (nAMD) with a portfolio of two products in the pipeline. We aspire to achieve this through a relentless commitment to patients, innovation, ensuring access to life‑changing therapies, and collaborating with healthcare systems, governments, and payers to make treatments available to those who need them most. Our focus is on patients, scientific rigor, and flawless execution—bringing breakthrough therapies to those who need them. Position Overview We are currently recruiting for...

Cleaning Verification Scientist, Pharmaceutical Analytical Sciences The Pharmaceutical Analytical Sciences group has an opening for a second shift Scientist based in Rahway, NJ. Join us and experience our culture first-hand - one of strong ethics & integrity, diversified experiences, exceptional science, and a resounding passion for improving human health through innovative drug delivery technologies and predictive analytical tools. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. In your role as Scientist, you will be part of a team of scientists working on cross-functional scientific...

We are seeking applicants for a Scientist position to join our Vaccine Analytical Research and Development team located in West Point, PA. The Scientist is a laboratory-based, scientific role tasked with solving complex analytical problems at the interface of biology, chemistry, and lab informatics disciplines to enable development of Vaccines. In this role, an individual will work with a team of scientists to develop state-of-the-art analytical techniques, such as separations of small molecules, polymers, proteins, conjugates and nanoparticles (FPLC, HPLC, CE), spectroscopic techniques (NMR, UV-VIS/IR/Fluorescence), virology, immunoassay and classical wet chemistry techniques. The individual should have knowledge of analytical techniques...

Senior Scientist, Process Cell Sciences (PCS) at Rahway, NJ The Biologics Process Research & Development organization within our company's Research Laboratories is responsible for developing the drug substance manufacturing processes for our company's biologics pipeline. We work closely with colleagues in Discovery, Pre-clinical and Early Development to rapidly develop manufacturing processes for diverse biotherapeutics, and efficiently manufacture material to supply clinical trials. We are also responsible for commercial process development and development and implementation of new manufacturing technologies. We work with our partners in our company's Manufacturing Division to commercialize and launch new products. We are seeking a highly motivated...

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

Our company's Quantitative Pharmacology and Pharmacometrics (QP2) Department is seeking a Team Leader (Executive Director) to support our rapidly expanding immunology pipeline. Immunology has been a strategic growth area for our company during the last years including an exciting late-stage pipeline including tulisokibart and a deep emerging pipeline consisting of traditional and newer modalities. This Team Leader brings deep disease area knowledge in immunology with strategic thinking to drive model-informed decision-making in our immunology portfolio in an end-to-end manner to gain competitive advantage. The individual has a strong understanding of the quantitative pharmacology global regulatory landscape to oversee and deliver...

Associate Principal Scientist 2nd Shift GMP Supervisor, Pharmaceutical Analytical Sciences The Pharmaceutical Analytical Sciences group has an exciting opportunity for an Associate Principal Scientist 2nd Shift GMP Supervisor based in Rahway, NJ. Join us and experience our culture firsthand - one of strong ethics & integrity, diversified experiences, exceptional science and a resounding passion for improving human health through innovative drug delivery technologies and predictive analytical tools. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. The Associate Principal Scientist will serve as the scientific...

POSITION OVERVIEW – Basic Functions & Responsibility Essential functions include, but are not limited to The Technician {Technical), Operations role is an excellent opportunity for individuals with experience in manufacturing and/or packaging operations who are proficient with basic mechanical/electrical equipment troubleshooting, maintenance, and repair. This role will serve as the first responder to challenges that arise with manufacturing and packaging equipment, effectively diagnosing and addressing technical issues. Key responsibilities include following manufacturing and packaging requirements, adhering to Good Manufacturing Practices (GMP), and completing daily tasks according to established procedures under the Operations Manager's guidance while collaborating with team members to...

À propos du poste Nous recherchons un(e) Directeur/trice de Business Unit ambitieux(se), stratégique et doté(e) d’un fort sens commercial pour piloter et développer notre activité Ruminants France en Santé Animale. Rattaché(e) au Directeur Général, vous aurez la responsabilité complète du compte de résultat (P&L) et serez garant(e) du déploiement national des stratégies marketing, techniques et commerciales. Ce poste offre l’opportunité de façonner la stratégie de l’activité, de constituer des équipes hautement performantes, de stimuler l’excellence opérationnelle et de créer un impact durable pour les clients et la santé animale. Responsabilités clés Piloter la mise en œuvre nationale des stratégies marketing,...

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. The Clinical Safety Statistics (CSS) group within BARDS supports proactive assessment, transparent communication, and effective management of product risk profiles across our company Research Laboratories pre- and post-marketing development stages. Responsibilities Provide statistical support for the evaluation of clinical safety at...

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. The Clinical Safety Statistics (CSS) group within BARDS supports proactive assessment, transparent communication, and effective management of product risk profiles across our company Research Laboratories pre- and post-marketing development stages. Key responsibilities for the position Provide statistical support and leadership for projects...

The Mixed Modalities team within Sterile Product Development is responsible for developing parenteral dosage forms (injections, implants, ophthalmic and inhaled products) for small molecules, intermediate modalities, and biologics from preclinical development through commercialization. Our development teams ensure robust formulation, primary packaging, sterilization strategy, and manufacturing process selection through deep scientific understanding and characterization, enabling scalable processes without compromising product quality, safety, efficacy, or delivery. This role is a technical leadership position with a strong focus on sterilization science and sterility assurance across drug products, primary containers, devices, and combination products, with specific focus on Intravitreal Product Development. The successful candidate...

Associate Director, Engineering Our Research Scientists are our Inventors. We identify and target steps in disease mechanisms or pathways that could be inhibited or enhanced. Our goal is to isolate a compound that is effective against a disease target. Using innovative thinking, state-of-the-art facilities, and robust scientific methodology, we collaborate to discover the next medical breakthrough. Seeking a candidate for a leadership position in our Research & Development Division Biologics Pilot Plant (BPP) Process Operations Team. We are recruiting a highly motivated and experienced person to Lead end-to-end program management for clinical manufacturing campaigns, with a focus on campaign...

The Pharmaceutical Analysis & Digital Technologies (PADT) External Capabilities, Validation, and Compliance (ECVC) department of our Research Laboratories Division is seeking applicants for a for a Senior Specialist position available at the Rahway, New Jersey research facility. The Stability and Sample Management Senior Specialist will work as a part of the integrated Stability Operations team and drive a culture of quality and operational excellence across the global analytical network. The Stability and Sample Management Senior Specialist will oversee and support GMP stability and sample management logistics in collaboration with our analytical scientists. The key responsibilities of this role will include...

Our Marketing teams are passionate about bringing our medicines and vaccines to our customers around the world. Through digital listening and patient analytics, we are able to understand our customers’ needs and strive to provide solutions to meet them. The position is based out of Upper Gwynedd, PA, reporting directly to the Associate Director, U.S. Vaccine Portfolio Marketing Strategy & Implementation Lead. Responsibilities will include, but not limited to Promotion Management Directs projects to ensure that all resources meet the objectives of customer and brand marketing teams. Develops organized customer tools and resources for Account Executives and across multiple engagement...

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 use innovative thinking, state-of-the-art facilities, and robust scientific methodology, we collaborate to discover the next medical breakthrough. As a Senior Scientist in the multiscale separations team within the Separations Sciences team of Analytical Enabling Capabilities, you will work within a highly collaborative team to enable the advancement of the development pipeline. You will be primarily responsible for chromatographic isolation of pharmaceutical API and impurities from analytical scale to semi-prep scale and prep scale, covering...

Applications are sought for an opportunity in the Vaccine and Advanced Biotechnologies (VAX) Process R&D department, which is part of our Company's Research Labs division of our Company's he individual will support our Company's downstream process development efforts for Vaccine programs at West Point, PA. Vaccines and Advanced Biotechnologies (VAX) Process R&D is responsible for the development and clinical manufacturing of Drug Substance (DS) and Drug Product Intermediates (DPI) for the vaccine and advanced therapy pipeline, spanning from preclinical to commercialization stages. We are part of the Process R&D organization, which enables modality-agnostic DS/DPI process development and clinical manufacturing for...

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

The Pharmaceutical Analysis & Digital Technologies (PADT) External Capabilities, Validation, and Compliance (ECVC) department of our Research Laboratories Division is seeking applicants for a for a specialist position available at the Rahway, New Jersey research facility. The Sample Management Specialist will work as a part of the integrated Stability Operations team and drive a culture of quality and operational excellence across the global analytical network. The Sample Management Specialist will oversee and support GMP stability and sample management logistics in collaboration with our analytical scientists. The key responsibilities of this role will include Collaboration with internal and external partners in...

Entry-Level Automation Associate Specialist Location Elkton, VA | 12‑Hour Rotating Shifts / Days and Nights Are you looking for an exciting opportunity with a rapidly growing pharmaceutical manufacturer? If so, this role offers a unique opportunity to launch your engineering career supporting highly automated, life‑saving manufacturing operations. At our Elkton, Virginia campus, located in the Shenandoah Valley along the Shenandoah River and near the Blue Ridge Mountains, we are seeking entry‑level engineers to support and sustain manufacturing operations through hands‑on automation technical support in a 24/7 manufacturing environment. Position Overview This role is an operations‑focused, shop‑floor automation support position. The...

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

Our Future Talent Program features co-operative assignments that last up to 6 months and will include one or more projects. These opportunities in our Global Services division can provide you with great development and a chance to see if we are the right company for your long-term goals. Our Support Functions deliver services and make recommendations about ways to enhance our workplace and the experience of working at our organization. The vision for the Global Workplace and Enterprise Services (GWES) based in Pennsylvania is to improve patient’s lives by providing world-class facility services & solutions that enable innovative research, medicines,...

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 Scientist Cell Based Sciences Vaccines The Analytical Research and Development team in West Point, PA is seeking an exceptional scientist who is passionate about innovative science and analytical solutions that enable and accelerate process and product development. The Senior Scientist within the department of Cell Based Sciences will join our vaccines team in West Point, PA. The Senior Scientist will play a key role with the primary focus on the design, execution, and interpretation of method development, optimization, and transfer of cell-based assays and immunoassays for drug substance and drug product release, stability studies, and in-depth product characterization to...

Reporting to the Director of Strategy & Field Enablement (STREAM), the Field Enablement Planning & Execution Associate Director will join the team responsible for the development, execution, and governance of end-to-end field enablement project management and process improvement including sales force restructuring strategy and execution, product launch support, field readiness efforts, and other field related initiatives for the US Market. This individual will work collaboratively with a diverse group of stakeholders and manage the complexity across headquarter functions to facilitate a seamless operational experience for field sales, account management, field access, and other field teams across our US HH commercial...

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

The Senior Administrative Associate provides proactive, high-quality, flexible and reliable administrative support to the Head of DSCS Digital Technologies. This role assists with administrative functions relating to organization and communication across the team and ensures the efficient operation of team members. We are seeking candidates who are proactive and act with a sense of urgency, thrive in complexity, demonstrate resilience, and model the highest caliber of values and standards. Candidates must have an interest in and ability to work successfully in a fast paced, complex work environment. The ideal candidate is a highly motivated individual capable of prioritizing work, demonstrating...

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

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. The Utility Specialist Engineer is a member of the Plant Engineering team providing technical support to the Wilson Site. The site includes an Energy Center, Vaccine Manufacturing Facility, Quality Labs, and a Packaging facility. This support position will focus on investigation of utility/facility system excursions, system improvements and optimizations. The incumbent will also be responsible...

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 Thoracic Oncology. The Executive Director, PDT Lead will manage the entire cycle...

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

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

The primary activities include and are not limited to the following Overall administrative/clerical duties requiring analytical ability, independent judgment and problem-solving skills Working independently, or in teams, as needed and relevant to complete work assignments and various tasks. Communication Skills must be at a level to effectively interact with our company's executives and internal/external stakeholders to maintain workflow. Knowledge of relevant Company policies and practices Interactions with internal and external stakeholders Administrative support for the HR hiring process in filling open positions on the team Support for calendar events, i.e., meeting scheduling, video conferencing, room reservations Use of MS-SharePoint and...

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

This is a great opportunity to be a part of the Strategy & Field Enablement (STREAM) Team within the Field Experience & Patient Access (FE&PA) business area responsible for enabling an optimized customer-facing organization across the US Market. We are seeking a highly talented, motivated, and experienced Field Enablement Planning & Execution Senior Specialist to join our team. The ideal candidate will operate at the intersection of strategy, program orchestration, and day-to-day execution across complex, cross-functional initiatives that enable an optimized customer-facing organization in the U.S. Market. This individual will work collaboratively with a diverse group of stakeholders and manage...

The Future Talent Program features internships that last up to 12 weeks and will include one or more projects. These opportunities in our Research and Development Division can provide you with great development and a chance to see if we are the right company for your long-term goals. Our Research Scientists are our Inventors. Our goal is to identify pharmacological agents that are effective against disease targets. We leverage innovative thinking, state-of-the-art facilities, robust scientific methodology and a collaborative environment to discover world changing medical breakthroughs. The Cellular Pharmacology group in the department of Quantitative Biosciences at a company of...

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

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

Reporting to the Sr Director/Director/Principal Scientist/Sr Principal Scientist in Pre-approval Pharmaceutical CMC is responsible for developing and implementing CMC regulatory strategies for our Company's pharmaceutical pipeline products in accordance with global regulations and guidance and is responsible for the preparation and submission of CMC dossiers for all assigned development products. Primary responsibilities include, but are not limited to Regulatory Responsibilities Serve as a CMC Product Lead for assigned products and be accountable for the delivery of all regulatory milestones through product development including assessment of the probability of regulatory success together with risk mitigation measures. Lead development and execution of...

The Pharmaceutical Analytical Sciences team has an opening for a director based in Rahway, NJ. Join us and experience our culture first-hand - one of strong ethics & integrity, diversified experiences, exceptional science, and a resounding passion for improving human health through innovative drug delivery technologies and predictive analytical tools. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. In this role, the Director will lead a team of specialists and scientists in Rahway supporting various GMP analytical activities including cleaning verification, solvent release, and...

Basic Functions & Responsibility Essential functions include, but are not limited to The Senior Specialist, Engineering will provide support for packaging operations in a range of capacities including analysis of operating performance, management of key operational data within SAP, application of advanced problem-solving capabilities, strengthening compliance posture and inspection readiness, and investigating and authoring deviations related to unplanned events. PRIMARY ACTIVITIES Primary activities include, but are not limited to Lead teams to identify, prioritize, and implement improvements related to Safety, People, Quality, Delivery, and Cost via detailed analysis of operating performance trends. Lead structured problem solving (i.e. 5 Whys, Fishbones,...

Field Access Manager The Field Access Manager (FAM) serves as the subject-matter expert on access related issues for healthcare professionals (HCPs) and healthcare organizations (HCOs), and will work cross-functionally with patient support, market access, and field sales to support timely patient access to therapy. The FAM will provide information to providers on access processes, reimbursement issues, and support patient assistance programs, all while ensuring compliance with healthcare regulations. The FAM role is a remote/field-based role that proactively provides approved education to defined accounts within an assigned geography on matters related to access and coverage to facilitate appropriate patient access. The...

For over 130 years, we have pioneered groundbreaking science. Today, we are driven by continuous innovation to develop breakthrough medicines, vaccines and technology. Rooted in direct experience on the farm and in the clinic, we work hand in hand with our customers every step of the way. Our singular focus is to empower those who care for animals, helping them manage their vital responsibility with confidence. Because when it comes to animal health, no one sees it like we do. The Sourcing Specialist is responsible for sourcing and negotiating the supply of various materials and services, with a primary focus...

The Microbial Process Operations (MPO) Team is seeking a Principal Scientist with expertise in microbial process development for the production of enzymes. Our team is part of Biocatalysis within the Small Molecule Process Research & Development (SMPRD) group, focused on advancing technologies for the manufacturing of a diverse small molecule portfolio. As a scientific leader, the successful candidate will contribute to and help translate scientific and platform strategies into experimental execution, ensuring robust, scalable, and compliant microbial fermentation processes that meet or exceed performance targets. The chosen candidate should possess strong interpersonal, communication, and collaboration skills, and should embrace and...

Essential functions include, but are not limited to The Specialist, Engineering will provide support for packaging operations in a range of capacities including analysis of operating performance, management of key operational data within SAP, application of advanced problem-solving capabilities, strengthening compliance posture and inspection readiness, and investigating and authoring deviations related to unplanned events. Primary activities include, but are not limited to Lead teams to identify, prioritize, and implement improvements related to Safety, People, Quality, Delivery, and Cost via detailed analysis of operating performance trends. Lead structured problem solving (i.e. 5 Whys, Fishbones, etc.) and implement corrective actions to prevent...

The Associate Director, Portfolio Resourcing actively manages the relationship with the functional areas regarding the project study costs and resource forecasting data both ad hoc and on set frequencies. In this role the individual will collaborate across multiple functional stakeholders in identifying, establishing, validating and managing the resource demand to complement our portfolio demand. Primary activities/responsibilities include Manage Global Clinical Development (GCD), and as requested, Global Clinical Supply (GCS), and Early Development, global headcount, capacity, and resource planning in support of clinical trial execution, based on our Company's authorized and projected Book of Business (BoB). Ensure logic checks are applied...

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

The Microbial Process Operations (MPO) Team is seeking a Director to provide operational, technical, and strategic leadership for MPO laboratories and capabilities supporting enzyme process development and characterization. Our team is part of Biocatalysis within the Small Molecule Process Research & Development (SMPRD) group, focused on advancing technologies for the manufacturing of a diverse small molecule portfolio. The Director will collaborate cross-functionally to shape departmental and project strategy, and drive operational excellence, ensuring robust, scalable, and compliant microbial fermentation processes. The chosen candidate should possess strong interpersonal, communication, and collaboration skills, and should embrace and model our core values of...

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

Our company's Infectious Disease and Vaccines group is seeking applicants for a Research Scientist position in the HIV Discovery area. This hands-on laboratory role contributes to in vivo studies, standardized biological assays, and development of novel biomarker assays (ELISA, qPCR, and related technologies). Candidates must be comfortable working with HIV-positive materials (laboratory strains and animal/patient-derived samples) and performing small-animal handling and procedures. The role requires strong organization, communication, and a willingness to learn new equipment and automation platforms. Key responsibilities Support and execute in vivo rodent studies, including cage maintenance, animal handling, dosing (IP, SQ, IV, PO), and blood/tissue collection....

The Pharmaceutical Analytical Sciences group has an opening for a Scientist based in Rahway, NJ. Join us and experience our culture first-hand - one of strong ethics & integrity, diversified experiences, exceptional science and a resounding passion for improving human health through innovative drug delivery technologies and predictive analytical tools. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. In your role as Scientist, you will be part of a team of Analytical Chemists working on cross-functional scientific teams to enable novel small molecule, peptide,...

J ob description This position will be responsible for leading and implementing medical device and combination product design controls for both new products and inline products from early design concept definition through commercialization to support regulatory filing, product launch, and post-market surveillance. The role will also be responsible for leading and supporting continuous improvement initiatives related to design control and risk management processes for combination products. This includes identifying process inefficiencies using operational excellence tools and ensuring alignment with global regulatory requirements (e.g., FDA 21 CFR Part 820, ISO 13485, ISO 14971). This position will interact with cross-functional development teams...

The Mixed Modalities team within Sterile Product Development is responsible for developing parenteral dosage forms (injections, implants, inhaled, ocular) for small, intermediate, and large molecules from preclinical toxicology studies to commercialization. Our development teams ensure robust composition, primary packaging/device, and process selection through deep fundamental understanding and characterization such that the process is scalable without compromising stability, safety, efficacy, and delivery. During development, we leverage smart experimental design, cutting edge analytical tools, and predictive approaches to inform molecule, formulation, and process selection. In summary, our team enables the translation of preclinical candidates into non-oral drug products. We are seeking a...

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

The Sterile Product Development group is responsible for the development of parenteral dosage forms, including long‑acting injectables (LAIs), across small molecules, peptides, and biologics from preclinical development through commercialization. Our teams enable robust and scalable drug product and delivery solutions through deep scientific understanding of formulation, drug–excipient interactions, delivery system performance, and manufacturing processes, ensuring product quality, safety, efficacy, and patient‑centric design. This role is a Senior Principal Scientist–level technical leadership position with a primary focus on primarily late-stage development of long‑acting injectable drug products, including depot formulations, extended‑release systems, and injectable sustained‑delivery technologies. The successful candidate will serve as...

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

Assurer la préparation et le suivi des dossiers de clôture mensuelle, trimestrielle et annuelle dans son secteur d'activités et procéder aux analyses et validations correspondantes en accord avec les process établis par le BSC (Business Services Center). Analyser, investiguer et résoudre toute question comptable demandée par le BSC, l'organisation Finances du Groupe, FP&A et mettre en place les actions nécessaires correspondantes. Communiquer régulièrement avec ses différents interlocuteurs et anticiper tout évènement pouvant avoir un impact significatif sur les comptes. Déterminer les écritures comptables complexes ou exceptionnelles en réunissant les éléments et procédant à toute analyse comptable préalable, avant communication au...

Role Overview The value team in Research and Development IT team brings together product management, engineering, and data science expertise to enable data and technology products and services that accelerate our scientists' ability to discover and develop innovative medicines that change the course of human health. Our IT team operates as a business partner proposing ideas and innovative solutions that enable new organizational capabilities. We collaborate internationally to deliver the services and solutions that help everyone to be more productive and enable innovation and advance the drug discovery and development pipeline. We are seeking a highly skilled Software Engineer to...

The Future Talent Program features co-operative assignments that last up to 6 months and will include one or more projects. These opportunities in our Manufacturing & Supply Division can provide you with great development and a chance to see if we are the right company for your long-term goals. This position will report to vaccine production or engineering management and support ongoing operational activities. Given the close interaction with actual Good Manufacturing Practice manufacturing, candidates need to be prepared to comply with Good Manufacturing Practice gowning restrictions for some of their activities (e.g. remove jewelry, remove make-up, remove false nails,...

An amazing opportunity has arisen for a Regional Ruminant Business Lead. This position will be responsible for ensuring alignment between the Global Ruminant Business Unit and the Regional Commercial organizations for all initiatives relating to the execution of the Business Unit strategy, acting as the voice of the Global Ruminant Business Unit with Regional Leadership and the voice of the Region within the Global team. This role can be based in any country where our company has a presence, preferably the United Kingdom, Portugal, Spain, or Belgium. This role will have a strong emphasis on project execution, with an initial...

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

Under the direction of EHS Director, the EHS Associate Director will be responsible for providing technical and regulatory support and implementation of all necessary measures and initiatives required by federal, state and local regulations pertaining to environment and safety protection at the Durham, NC sites. Provides direction and is responsible for planning, developing and reviewing environmental, safety and industrial hygiene programs for our manufacturing division. Job description and Responsibilities Responsible for providing compliant environmental, health, and safety (EHS) programs to operating and support departments at the Durham sites. Integrates EHS programs into daily operations to assure regulatory compliance, achieves continuous...

The Future Talent Program features co-operative assignments that last up to 6 months and will include one or more projects. These opportunities in our Manufacturing & Supply Division can provide you with great development and a chance to see if we are the right company for your long-term goals. Under the guidance of Reliability, Maintenance and Utilities Engineers, the Manufacturing and Reliability Engineering Co-op will support the on-going operation of Vaccine Manufacturing facilities and equipment as a member of the Engineering, Maintenance and Utilities (EMU) organization. Given the close interaction with actual Good Manufacturing Practice (GMP) manufacturing, candidates need to...

Sr. Specialist – Business Insights & Analytics, Advanced Analytics - US Vaccines & ID We are seeking a Business Insights Analytics Sr. Specialist focusing on data science and analytics to join our team. This role will collaborate with the Digital Human Health (DHH) area to utilize data for generating actionable insights. In this role, the Sr. Specialist will act as a strategic thought partner for marketing stakeholders and internal DHH partners actively collaborating and providing data driven insights to help shape commercial decisions. They will partner with cross-functional teams in designing and delivering scalable solutions and valuable insights that address...

Our Regulatory Affairs team in General Medicine advances medical innovation to patients by establishing clear, timely, and robust strategies for registration enabled by engagement with global health authorities. We work across functions and geographies to advance development programs and maintain licensure for the General Medicine portfolio worldwide. We seek a leader with a growth mindset, demonstrated by intellectual curiosity and the ability to navigate complex regulatory challenges with rigor and professionalism. Position The Executive Director, Regulatory Affairs Liaison reports to the Vice President (VP), General Medicine, and is accountable for defining and executing global regulatory strategy for assigned ophthalmology...

In our Company's Research Labs, we identify and target steps in disease mechanisms or pathways that could be inhibited or enhanced. Our goal is to isolate a compound that is effective against a disease target. Using innovative thinking, state-of-the-art facilities and robust scientific methodology, we collaborate to discover the next medical breakthrough. Seeking candidates for a unique and exciting opportunity to bridge across two pilot scale facilities in VAX and Biologics Process Research and Development. The Vaccines and Advanced Biotechnologies Process Research & Development (VAXPR&D) and Biologics Process Research & Development organizations within our Company Research Labs are broadly responsible...

Overview The Environmental, Health, and Safety (EHS) Sr. Specialist is accountable for supporting and maintaining an efficient and effective health, safety and environmental management system for the De Soto, KS manufacturing and research site. This role will ensure compliance with EHS regulations and promote best practices across various operation units, fostering a culture of safety and continuous improvement. The successful candidate will be physically located at the main campus at DeSoto, KS. Reporting Structure The Sr. Specialist of EHS sits within the Global Safety & Environment organization, and reports to the Associate Director of Safety & Environment of De Soto...

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 discovery capabilities and world-class R&D with the purpose of turning breakthrough science into life-changing medicines. We are seeking a Senior Scientist to join Biologics Design and Display team in the Boston Discovery Biologics group. The successful candidate will be an integral member of the team responsible for conducting in vitro display campaigns to generate novel therapeutic hits and optimized leads. They will directly contribute to the discovery of novel biologics as well as platform build and...

Postdoctoral Research Fellow – Crystallization Sciences Be a part of the legacy Postdoctoral Research Fellow Program Our Research Laboratories’ Postdoctoral Research Fellow Program aims to be a best-in-industry program for industrial postdoctoral researchers, designed to provide you with an academic focus in a commercial environment. With the resources, reach, and expertise of a large pharmaceutical company, postdoctoral researchers will be positioned to excel in an institution committed to breakthrough innovation in research and discovery. Position Overview We are seeking a highly driven and motivated postdoctoral research scholar to join the Materials & Biophysical Characterization group within Analytical Research & Development....

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

Wat je hier maakt, gaat de wereld over! Draag bij aan innovatieve vaccins die het welzijn van dieren verbeteren en voedselzekerheid wereldwijd versterken, sluit je aan bij ons team in De Bilt als Bioprocess Technician Welkom in ons team In De Bilt zoeken we enthousiaste Bioprocess Technicians met oog voor detail, die willen bijdragen aan een innovatieve biotechomgeving. Op onze productielocatie maken we vaccins voor pluimvee die in meer dan 100 landen worden gebruikt. Zo verbeteren we dierenwelzijn én versterken we voedselzekerheid wereldwijd. Bij ons draait het om samenwerking en groei. Je werkt samen met collega’s van diverse achtergronden in...

Global Project and Alliance Management (GPAM) resides within our company Research and Development (R&D) organization, which is known as our company's Research & Development division. The Project, Portfolio and Alliance Managers in GPAM are core members of discovery, development, and alliance teams at our company and lead these cross-functional teams to deliver products that improve human health. The GPAM Alliance Managers focus on achieving the goals of alliance collaborations by ensuring activities, resources, communications, and decisions are coordinated and maximized with our R&D partners. Position Description/Summary The Director, Strategic and Sponsored Alliances is responsible for establishing, managing, and maximizing the...

Position title · Associate Director, Global Marketing Swine Technical Nutritionist Organizational unit Animal Health — Global Marketing - Swine Summary of the job The Global Marketing Swine Technical Nutritionist is a senior technical role within our company's Animal Health’s Global Swine Business Unit. This person will provide high-level global nutrition and technical support to marketing, commercial and R&D teams across product lifecycles, ensuring nutritional science drives product positioning, claims and field adoption. The role blends applied swine nutrition expertise with strategic marketing support and global stakeholder engagement to advance product development, extension materials, and customer-facing technical resources. The role requires...

Location Rahway, NJ (supports multiple sites) Role Summary This role serves as the senior technical and product leader for pilot plant and manufacturing-facing research automation platforms. The Associate Director is accountable for strategy, architecture, delivery, and operational excellence of plant-side automation and OT infrastructure, while also providing hands-on technical leadership and oversight of system integration, cybersecurity, and regulated operations. This position owns the plant automation technology portfolio end-to-end, from concept and design through validation, deployment, support, and lifecycle management. Key Responsibilities Define and own the strategy for pilot plant and plant-facing research automation platforms Act as technical lead and single...

The Future Talent Program features Cooperative (Co-op) education that lasts up to 6 months and will include one or more projects. These opportunities in our Research and Development Division can provide you with great development and a chance to see if we are the right company for your long-term goals The Precision Genetics group within Data, AI & Genome Sciences (DAGS) is seeking a self-motivated Co-op student (up to 6 months) to support large-scale proteomics, genetics, and multi-omics projects. You will work with scientists to develop reproducible analytical frameworks that integrate biobank-scale proteomic and other omics data to accelerate biomarker...

The Senior Engineer (2nd Shift) in our Company's Research Labs (Pharm Ops Engineering) provides engineering and compliance support for the FLEx (Formulation, Laboratory & Experimentation) Center in Rahway, NJ. This role supports non‑sterile process equipment and utilities used in the manufacture of oral solid dosage (OSD) products across clinical, developmental, and commercial programs. The position operates with minimal supervision and serves as a key technical and compliance resource during second‑shift operations. Education Bachelor’s degree in engineering with a minimum of 5 years of experience supporting pharmaceutical manufacturing operations for oral solid dosage (OSD) formats Required Experience and Skills Demonstrated commissioning...

The Associate Specialist in Supply Chain Management will provide support to various groups within Wilson Supply Chain Management, including Planning, Logistics, Master Data/New Products, and Change Control. This individual will serve as a key contributor within the Supply Chain function, utilizing data, information, and available tools to deliver valuable insights that help drive business performance. The candidate is expected to focus on data discovery and preparation, model development and data mining, as well as evaluating options and presenting recommendations. Their work will span a variety of projects aimed at enhancing service levels, reducing cost and risk, improving cash flow, and...

In this role, the Contract Lifecycle Management (CLM ) Product Line Lead will drive the strategic implementation and ongoing evolution of its enterprise CLM platform, with a focus on DocuSign CLM. This individual will play a critical role in a multi-year, complex global transformation program, serving as the primary business-facing product lead across internal stakeholders, the selected systems implementation partner, and the software provider. The successful candidate will be responsible for defining the product line’s priorities and vision, translating business needs across 10+ functional areas and 40+ markets into actionable requirements, and driving successful delivery of CLM capabilities across the...

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

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

The Pharmaceutical Analysis & Digital Technologies (PADT) department of our Research Laboratories Division is seeking applicants for a senior specialist position in the GxP compliance and documentation team to support the global analytical organization. The position will be based at the Rahway, NJ research facility. The Compliance Senior Specialist will work as part of the integrated Compliance team and be pivotal in driving a culture of quality and operational excellence across a global analytical network. The key responsibilities of this role include Management and oversight of Good Manufacturing Practices (GMP) documentation, training, and standard operating procedures (SOPs) for the global...

As a Chronic Care Specialty Sales Representative, you will drive meaningful patient impact by leveraging our scientific expertise and serving as the primary contact for customers within your assigned territory. As a key member of the local Customer Team, you will collaborate closely with Account Executives, Integrated Delivery Systems leaders, and other field colleagues to deliver seamless, patient-focused solutions. Territory Assignment This is a field-based sales role responsible for covering the Poughkeepsie, New York territory. Additional areas of this territory include but may not be limited to Fishkill, New York and Newburgh, New York. Travel (%) depends on the needs...

The U.S. Oncology business within our company is a growing and dynamic part of our company. We have an exciting opportunity to join our dynamic marketing team focusing on intismeran autogene, a cutting-edge individualized neoantigen therapy (INT), which represents a transformative approach to cancer treatment, as part of our alliance partnership. We are seeking an Associate Director, US Oncology Marketing, Patient Experience Strategy Lead to shape the end-to-end patient experience for intismeran autogene. This role will define the foundational INT Patient Support Program (PSP) and Patient Experience strategy, and lead the go-to-market plans anchored to address key pain points in...

Join the US launch team for an investigational Phase III HIV prevention asset to design and execute strategic external partnerships that expand access to PrEP (Pre-exposure Prophylaxis). Reporting to the Executive Director, U.S. Commercial Leader (USCL), HIV PrEP, this hybrid role is based in Upper Gwynedd, PA with ~25% domestic travel. The Director will own partnership strategy and execution for Direct-to-Patient (DtP) and retail/community pharmacy channels, manage a small team, and partner across Marketing, Legal/Compliance, Regulatory, IAM (Integrated Account Management), Data & Analytics, Pharmacy, Communications, Learning & Development and Ecosystem Leads to operationalize DtP capabilities. Key Responsibilities Telehealth and Direct...

We are seeking a transformative digital product line leader to evolve our global digital commercial solutions and content enablement capabilities. As a key member of the Animal Health Commercial IT Leadership Team, you will be accountable for transforming how we enable digital customer engagement across the globe and for defining and advancing a modern product model for digital commercial solutions and technologies. You will own and enhance a portfolio of global solutions including mobile messaging, web (WordPress VIP), mobile applications, social media, content management platforms (Veeva PromoMats), and AI-enabled solutions. Building on this digital backbone and leading a team of...

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

Position Overview The successful candidate will be a contributing member of the DOI team, supporting initiatives that integrate artificial intelligence tools across scientific operations, automated authoring workflows, and laboratory operations. This role sits at the intersection of life sciences and data/computer science, and is well-suited for those with foundational experience in both domains who are eager to grow their skills in an applied, collaborative environment. The candidate will contribute to AI-driven solutions for scientific search, summarization, and information extraction, helping NDS scientists and operational teams access and synthesize relevant scientific knowledge more effectively. They will also support ongoing efforts to...

Sr. Specialist, Clinical Supply Operations (P3) Position Description The Sr. Specialist, Clinical Supply Operations (CSO) is responsible to support our clinical supply packaging & distribution operations at our company's Rahway, NJ site. This role will collaborate with a diverse range of stakeholders, subject matter experts, and customers both within and outside of Global Clinical Supply (GCS). Your responsibilities will be instrumental in driving innovative initiatives, ensuring operational efficiency, and maintaining compliance, all while supporting our commitment to business continuity. This role will report into Associate Director, Packaging & Distribution Support at our company's Rahway site. Key responsibilities of the Sr....

Associate Director, Strategic Forecasting The Associate Director, Strategic Forecasting, will be responsible for developing strategic forecasts for a set of products and indications, interpreting their implications, generating insights, and communicating them to the business to help execute the marketing strategy. The individual in this role will work extremely closely with other DHH functions, including Market Research, Data Science, and Payer Analytics to build a strong perspective on the market and asset situation and thus the inputs to the strategic forecast. She/he will also work very closely across a range of commercial stakeholders, including Global and Regional Marketing, Market Access, and...

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

The Senior Clinical Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new medicines in the Oncology Asset therapeutic area. Our company's Oncology Asset TA medicines are generally in transition from early to late clinical development. The Senior Clinical Director may manage the entire cycle of clinical development for their assigned studies including study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. Role Responsibilities Specifically, the Senior Clinical Director may be responsible for Evaluating pre-clinical and translational work for the purpose of generating early clinical development plans and Investigational New Drug applications Developing...

Are you looking for an exciting opportunity with a rapidly growing pharmaceutical manufacturer? If so, then this is the opportunity for you! FUNCTION Essential functions of the position include, but are not limited to, the following reporting to a Utility Manager, operates and maintains equipment and machinery used to generate sufficient steam pressure to operate a cogeneration power plant which includes and two (2) natural gas turbines. Monitors and operates systems including main steam distribution and condensate return, feedwater treatment, natural gas, fuel oil, potable water, fire prevention, compressed air, chilled water, condenser water, wastewater treatment, and electrical grid. Maintains...

I. GENERAL JOB SUMMARY a. Responsible for supporting the plant operations at the Durham facility. Technicians operate 7-days per week utilizing different shifts. Technicians will provide services in numerous areas within site services. Technicians must be forward thinking individuals who are able to flow to the work. Functioning as a member of the Site Services Team and operating in an empowered team environment. Technicians are responsible for safeguarding all company personnel, property, and assets, preventing theft or loss of company property, and enforcing company, local, state, and federal rules, and regulations. Technicians will have responsibility for access control of...

The Analytical Commercialization Technology (ACT) group within Analytical Chemistry in Development and Supply (ACDS) is seeking applicants for a Senior Scientist position available at the Rahway, NJ site. The successful candidate will utilize innovative analytical characterization technologies to drive late-stage pharmaceutical drug product development and commercialization. The Senior Scientist responsibilities include, but not limited to, analytical method development and validation, drug product testing and analytical investigations in a cGMP environment, drug product and manufacturing process characterization, drug product stability studies, specification development, manufacturing process scale-up and validation support, preparation of Chemistry, Manufacturing, and Controls (CMC) documents for global regulatory submissions,...

HVAC Technician, (O3) HVAC&R In Primary Posting Language The HVAC&R Technician is responsible for providing equipment troubleshooting and maintenance support for ongoing facility facility/manufacturing operation and support growth initiatives at the site. Assists in and develops standard operating procedures (SOP's) and preventative maintenance (PM's) plans. Responsible for written documentation of activities. Responsible for SAP transactions and change control activities including spare part lists and Preventative Maintenance (PMs) plans. Actively supports, participates and embraces an inclusive team culture including significant interaction with Operations, Quality, Automation, Technology, and other groups as required. The HVAC&R Technician will provide maintenance supporting vaccine process...

Associate Principal Scientist, Analytical Commercialization Technology The Analytical Commercialization Technology (ACT) group within Analytical Chemistry in Development and Supply (ACDS) is seeking applicants for an Associate Principal Scientist position available at the Rahway, NJ and West Point, PA sites. The successful candidate will utilize innovative analytical characterization technologies to drive late-stage pharmaceutical drug product development and commercialization. The Associate Principal Scientist position is seeking applicants with deep knowledge and experience in inhalation product development and characterization. The Associate Principal Scientist responsibilities include, but not limited to, analytical method development and validation, drug product testing and analytical investigations in a cGMP...

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

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...

The Enterprise Strategy Office (ESO) develops, implements, and drives enterprise strategy in support of our company, its customers, and other stakeholders. The scope of this group includes strategy development, strategy execution and value realization, enterprise strategic planning, risk management, and strategic venture investments in healthcare as part of our Global Health Innovation fund. Together, we identify business critical opportunities, frame and evaluate options, and ensure effective implementation and cross-functional engagement to realize impact. Oncology is a key area of focus for our company, and our portfolio is large, diverse and evolving rapidly. Within ESO, we provide deep strategic partnership in...

We are currently seeking an Associate Principal Scientist, Biomarker Operations Vendor Management to be an integral part of a Biomarker Operations team in our company’s translational medicine area. You will serve as a functional interface between internal project teams, internal molecular biomarker lab and diagnostic vendors. Your responsibilities will include maintaining a high level of vendor productivity, proactively assessing new capabilities and technologies, participating in external vendor audits and due diligence, ensuring both internal and external compliance, creation and adherence to vendor standardization and managing problem resolution. You will also closely partner with internal scientists and alliance and relationship managers,...

The Associate Director, US Oncology Marketing — Metastatic Lung Cancer HCP Strategy is a high-visibility, high-impact commercial leader responsible for shaping and executing growth-driving initiatives across the metastatic NSCLC portfolio. This role will refine and accelerate the marketing strategy to capture new opportunities in an intensely competitive and rapidly evolving treatment landscape. You will combine strategic rigor with flawless execution building clear plans, operationalizing them across cross-functional partners, and driving measurable outcomes. Success requires exceptional stakeholder management, the ability to influence at all levels, and the judgement to balance bold thinking with compliance and scientific integrity. The ideal candidate brings...

Are you looking for an exciting opportunity with a rapidly growing pharmaceutical manufacturer? If so, then this is the opportunity for you! I. GENERAL JOB SUMMARY The Manager, Plant Protection and Emergency Services, will be responsible for providing guidance, oversight, and management of the site’s emergency management and loss prevention programs for the Durham Hilleman, BCG and Teknika facilities. They will work with cross-functional teams to effectively and safely operate and maintain the emergency management organization and its systems to support all entities at the Hilleman, BCG and Teknika sites. The manager is responsible for ensuring site compliance with...

Site Inventory Coordinator . Key Responsibilities General warehouse work Under the guidance of supervision, supports inventory management in the receipt, disbursement, labeling, placement, and distribution of materials to supply or staging areas throughout the Rahway site. Utilizes and demonstrates proficiency with computer database systems that support and facilitate the entire procurement and inventory management program as well as any other supporting computer systems. Performs data entry and queries, maintenance, and reconciliation of inventory levels. Samples various production materials and chemicals for quality evaluation and handling associated paperwork. Performs shipping material identification or status control labels and prepares documents according...

Strategic Summary The Senior Automation Engineer is responsible for day-to-day operations support activities for process control systems in a vaccine manufacturing facility. the Senior engineer will be the lead engineer of a small team of 4-5 engineers providing day to day coordination of tasks, serving as the first point of escalation for the area, and acting as the primary automation change control approver. The automation technologies may include but are not limited to the following technologies Distributed Control Systems (Delta V), Programmable Logic Controllers (Allen Bradley), OEM systems to include Washers, Autoclaves, and purified water systems (WFI/Clean Steam). Key Responsibilities...

We are seeking an experienced and innovative Associate Principal Scientist to join the Process Analytical Technologies (PAT) team within Analytical Enabling Capabilities. In this role, you will collaborate with a cross-functional, highly engaged team to advance the development pipeline and support commercial manufacturing. The successful candidate will lead the development, validation, and implementation of in-line, on-line, and at-line PAT solutions for both small- and large-molecule modalities. Join our company and contribute to our mission of delivering innovative health solutions that advance the prevention and treatment of diseases in people and animals. Responsibilities Provide technical leadership for systematic assessment and deployment...

The Allflex/SenseHub Livestock Intelligence group, part of our company's Animal Health division, is the world leader in the design, development, manufacturing and delivery of solutions for animal identification, monitoring and traceability. 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 farmers’ hands, our solutions empower them to act in a timely manner to safeguard their animals’ health and wellbeing, while achieving optimal production outcomes for a healthy food supply. As the largest provider of animal identification technology, we meet growing customer needs by providing...

Become part of a team at the forefront of digital procurement innovation, advancing value engineering and automation to further strengthen how Procurement manages risk, operations, and supplier performance. You will lead two high‑impact automation initiatives - risk management and operations automation - while evolving a value engineering framework to improve cost transparency, track supplier performance, and ensure value realization. This is an ideal role for a technically savvy self‑starter who wants to leverage their technical background to drive direct, measurable business impact while expanding their influence and accelerating personal growth. What you’ll do Lead and deliver automation initiatives across Procurement...

Brief Description of Position The Associate Director Quality Systems & Compliance within Device Quality & Regulatory will support our company's Manufacturing Division QMS Topic 3.3 – MDCP Design Controls and lead continuous improvement initiatives that support every aspect of our business processes, systems, and data. The Associate Director will collaborate with cross-functional teams to identify opportunities for improvement, address internal/external audit observations and tackle challenges, balancing effective operations with transformative initiatives. The Associate Director will work with the manufacturing division's Topic 3.3 Owner and Business Owner and has responsibility for oversight and lifecycle management of procedures related to this specific...

Position Overview - Basic Functions & Responsibility As a member of the Device Quality & Regulatory QMS group, the Associate Director will participate in and/or lead various initiatives in support of our QMS Purchasing Controls and Device Supplier Management objectives and build QMS capabilities that touch every aspect of our business processes, systems, and data. The Associate Director will collaborate and interact with cross-function teams to identify opportunities for improvement and tackle challenges, balancing effective operations with transformative initiatives. The Associate Director, Quality System & Compliance will lead efforts to establish early commercialization Purchasing Controls processes and integrate the Device...

The Executive Director, Chemistry, Manufacturing, Control for Biologics (Biologics-CMC) is accountable for managing a team of CMC professionals and ensuring rigor in CMC regulatory strategy as well as delivery of high quality CMC submissions for late phase new modality biologics products. The Executive Director, as a Senior member of the Global Regulatory Affairs and Clinical Safety Chemistry, Manufacturing and Control organization ( GRACS CMC), will also manage significant projects as an extension of the overall GRACS CMC Leadership Team. This lead plays a critical role in driving alignment and execution globally across Regulatory CMC (Chemistry, Manufacturing & Controls), GRACS (Global...

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