Merck Job Trends

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

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

The Executive Director (ED) for US Medical Affairs (USMA) understands Our Company’s enterprise level strategies and leads cross-functionally with the Global Medical and Scientific Affairs Therapeutic Area (GMSA TA) teams to translate Global Value and implementation (V&I) goals into the relevant US country-level goals and priorities. The USMA ED level of responsibility and accountability is in alignment with the USMA core vision of advancing medical innovations that improve patient outcomes in the US and setting the foundation for impact around the globe. Thus, the USMA ED is responsible for the creation and execution of the overall therapeutic aligned US strategy...

Our Scientists are our Inventors. Using innovative thinking, state-of-the-art facilities, cutting-edge science, and technology, we partner to deliver the next medical breakthrough. We are seeking a collaborative, self-directed learner with a penchant for problem-solving and expertise in upstream bioprocessing to join Biologics Process Research & Development (BPR&D) as a Principal Scientist. BPR&D within Research Laboratories is on a mission to rapidly deliver diverse 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 a diverse and inclusive environment...

Translational Medicine is responsible for early clinical development of novel therapeutics, working in close collaboration with Discovery Sciences and late-stage Clinical Research across all therapeutic areas. Our team is focused on innovation and dedicated to translating breakthrough science into innovative medicines that extend and improve the lives of patients worldwide. Through clinical trials, we ensure the safety and efficacy of our pipeline and existing products to produce safe, effective, innovative medicine. The Early Clinical Scientist/ECS coordinates the design, planning and execution of early phase clinical trials with the Clinical Director and internal/external team members. Oversees trials within and/or across program(s)/therapeutic...

Position Description Under the direction of EHS Director, the EHS Associate Director will be responsible for leading a team of environmental, health and safety professionals, 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 West Point site. Provides direction and is responsible for planning, developing and reviewing environmental, safety and industrial hygiene programs and providing direct customer support specific to our global vaccine manufacturing and supporting operations at either a site or division level. Core Activities Plan, develop and implement EHS...

Our Research Scientists are our Inventors. Using innovative thinking, state-of-the-art facilities, and robust scientific methodology, we partner to deliver the next medical breakthrough. Biologics Process Research & Development (BPR&D) within our Company Research Laboratories are on a mission to rapidly deliver diverse 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 a diverse and inclusive environment for all. Beyond process development for pipeline biologics, we innovate and build next generation biomanufacturing technologies. Examples include investments for development...

Our Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines 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 Senior Director has primary responsibility for the planning and directing clinical research activities involving new or marketed Neuroscience Medicines. Our company's Neuroscience Medicines span all phases of clinical development (pre-clinical to post-licensure). With a focus on late-stage development, the Senior Director will manage the entire cycle of clinical development, including study...

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity, and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, inclusion, and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. Global Engineering Solutions (GES) is responsible for the design, construction, and delivery of advanced manufacturing facilities and laboratories worldwide. We provide premier engineering solutions in the pharmaceutical industry through technical innovation and project management to deliver important life-saving medicines and vaccines to patients....

Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. The Senior Clinical Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities...

The HR Organizational Readiness, Associate Director is an experienced employee engagement, change management and internal communications professional with a passion for driving innovative, employee-centric strategies that engage our company's workforce in high priority initiatives that are directly tied to our strategic priorities. This role will create and lead strategic, high-impact, high exposure programs that drive employee awareness, adoption, and recommendation of HR products and services, while simultaneously realizing our employee value proposition, and catalyzing a positive employee experience with HR products and services. Primary responsibilities Partner with HR Centers of Excellence to define and execute effective employee engagement plans that...

The Senior Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed cardiovascular and respiratory medicines. With a focus on late-stage development, the Senior Director will manage the entire cycle of clinical development, including 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 plan and investigational new drug applications Developing clinical development strategies for investigational or marketed cardiovascular and respiratory drugs Planning clinical trials (design, operational plans, settings) based on...

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

The Senior Specialist, Global Pharmacovigilance will be responsible for some or all of the following core activities Case review/approval for assigned products Expedited case submission according to timelines outlined in applicable regulations Case entry for non-PV-Works countries for assigned products Aggregate report preparation and submission to National Teams or Competent Authorities according to timelines outlined in applicable regulations Support national PV teams as applicable Product expert for assigned products Provide qualified answers to questions raised by internal or external stakeholders (e.g., Competent Authorities) for products for which the Senior Specialist is responsible PV Statement preparation in compliance with relevant regulations,...

The Biologics Analytical Research & Development department of our company Research Laboratories Division is seeking applicants for a Principal Scientist position available at its Kenilworth, New Jersey research facility. The Principal Scientist is a senior scientific role tasked with working closely with the group Director to define group 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 and working along others...

The Precision Genetics group within Data, AI and Genome Sciences (DAGS). Our department is recruiting a Senior Director, who will serve as the Computational Biology lead for Cardiometabolic Drug Discovery Data Science. We are seeking an experienced computational biologist with a proven track-record in applying human genetics to generate target/biomarker hypotheses and patient stratification strategies. This role will lead a team of bioinformaticians and data scientists to apply cutting edge AI/ML approaches to leverage our Company’s investments in human genetics and other multimodal data to support drug discovery in the cardiometabolic disease space. This work will help to inform discovery,...

FUNCTION Under the supervision of the Maintenance and Utilities Supervisor and direction of the maintenance team leader, installs, maintains, operates, calibrates, repairs and troubleshoots refrigeration, air conditioning and air volume equipment and associated control systems. In compliance with operating procedures, Company and Government regulations, and current Good Manufacturing Procedures, assures the quality of our products and services are of the highest priority. HVAC mechanics will perform maintenance on any equipment or facilities which their skills support in a compliant quality manner. HVAC mechanics are part of the Utilities Technician work group and will primarily share work assignments within their job...

Overview The Sr. Specialist in Biosafety and Biotechnology Solutions is responsible for managing an effective biosafety program while supporting production troubleshooting, vaccine process development, and key business initiatives at the Elkhorn Animal Health site. This role will ensure compliance with biosafety regulations and promote best practices across various departments, fostering a culture of safety and continuous improvement. Reporting Structure This position sits within the Global Safety & Environment organization and reports to the Director of Environment, Health & Safety at Elkhorn, NE; while also collaborating closely with the Director of Biotechnology Solutions. Key Responsibilities Biosafety Management Develop, implement, and maintain...

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

The Associate Vice President (AVP) / Companion Diagnostics will be responsible for leading the diagnostics strategy, bridging the continuum from Discovery Research through Late-Stage Clinical Development. The successful candidate will have an essential strategic and tactical role in overseeing the scientific direction of companion diagnostics (CDx). Specifically, the Diagnostics Lead will develop and execute diagnostic strategies and interact with various stakeholders to ensure alignment with clinical development timelines and regulatory requirements. Most importantly, the role requires overseeing CDx development, ensuring timely delivery of CDx solutions for pharmaceutical registration and launch. This individual is expected to stay up to date regarding...

Member of DS Operation working as part of a global team to support a fast-paced environment. Ensure conformance to established system architecture, security, regulations, standards and practices, and participate\drive their creation and upkeep. In addition to technical expertise must be proficient in managing projects through to completion, innovative, security focused, self-motivated and driven. The candidate will be a member of the global Tier 2 Directory Services Operations team which includes operational responsibilities across all supported LDAP compliant directory environments and core services within the organization. Good communication skills, documentation abilities and compliance experience required. Comfortable working in a team environment...

The Facility/Utilities 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 for leading plant engineering improvement projects and implementation of productivity enhancement initiatives. Responsibilities General Manages individual contributors (professional employees) and/or contractors Contributes to the performance and results of the utility department Adapts departmental plans and priorities to address resource and operational challenges Decisions are guided by...

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

We are a high-performing global team that helps our colleagues adopt new technology tools and integrate technology changes into their everyday work. We support our colleagues through change and help them embrace it. We have a customer-centric approach and always strive to provide the best user experience possible. Teamwork is important, and you’ll be collaborating with your colleagues cross-geographically on a daily basis. We are looking for an enthusiastic and motivated team member who is a self-starter, learns quickly and shows a keen interest in technology. In this role, you will be responsible for planning, managing, and executing training and...

Brief Description of Position The Imaging Lead (Sr. Principal Scientist) works with Clinical Imaging Scientists to support clinical trial teams in the use of medical imaging in clinical trials. The Imaging Lead provides leadership on the medical and scientific aspects of the use of imaging, and oversees the work of the Clinical Imaging Scientist to ensure that timelines and deliverables are met and of high quality. The Imaging Lead leads scientific and operational initiatives, and oversees the implementation of operational improvements by Clinical Imaging Scientists. This position will work closely with the Head of Clinical Imaging, Imaging Operations Lead and...

The Field Engagement Capabilities Team (FEC) is committed to delivering innovative, personalized, and compliant digital experiences to our users and customers. We translate customer needs into effective digital solutions that enhance engagement and drive meaningful outcomes. We are seeking a Senior Specialist with deep expertise in oncology and digital channel innovation to serve as a Field Digital Channel Subject Matter Expert (SME). This role will collaborate with Marketing/Promotion and agile Digital Engagement Teams to provide expert guidance on both Veeva CLM and Veeva Approved email channels. Reporting to the Field Digital Channel Lead, this role will manage cross-functional projects to...

Employee will be responsible for picking, packing, and metering small parcel shipments. Work will be completed within a clean, temperature-controlled warehouse. Employee responsibilities Lift up to 50lbs continuously, and up to 75lbs on occasion Pick orders within a pick zone and/or on a Powered Industrial Vehicle Pack orders within a packaging station, per pack out protocols Meter packages using a TMS system and stacking pallets as needed based on service level Clean areas on routine basis and documenting activities All activities documented on paper and within SAP (SAP is the WMS system used) Perform work to cGMP standards Cross train...

02 Utilities Technician Are you looking for an exciting opportunity with a rapidly growing pharmaceutical manufacturer? If so, then this is the opportunity for you! 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. Ability to perform routine maintenance tasks, work with and troubleshoot complex process systems, including but not limited to Utility Equipment (e.g. boilers, chillers,...

Our company is expanding its global Bacillus Calmette Guerin (BCG) vaccine production by adding an end-to-end laboratory capability located in the Durham, NC campus. The new facility will be used to produce the bulk active ingredient, finished product, and laboratory testing for the BCG vaccine. The Specialist, Quality Control participates in a team of analysts in the development, validation, and routine testing for the BCG Product. The position will focus on environmental monitoring, aseptic process simulation and support testing readiness in preparation for commercial production. The selected candidate will participate in equipment validation, process validation, and GMP laboratory readiness. The...

Purpose of Role The Site Analytical Sciences Senior Specialist role is responsible for supporting Analytical Procedure Life Cycle through end-to-end method lifecycle management including introduction of new analytical methods, analytical transfers, SME assessment for all analytical method & equipment performance qualification, investigations, product testing and technical rationale. This work will support pipeline and commercial products by utilizing expertise in the analytical areas of separations and chemistry. Activities Within Role Technical expertise to support New method introduction (Validation /Tech Transfer). New technology introduction. Assessment and implementation of changes for existing methods and equipment Change in technical element of method e.g. Parameter...

The Site Analytical Sciences Specialist role is responsible for supporting Analytical Procedure Life Cycle through end-to-end method lifecycle management including introduction of new analytical methods, analytical transfers, SME assessment for all analytical method & equipment performance qualification, investigations, product testing and technical rationale. This work will support pipeline and commercial products by utilizing expertise in the analytical areas of separations, biochemistry, and microbiology. Technical expertise to support New method introduction (Validation /Tech Transfer). New technology introduction. Assessment and implementation of changes for existing methods and equipment Change in technical element of method e.g. Parameter change Change in equipment/material element of...

Our Company is a trusted global leader in human and veterinary medicine, dedicated to preserving and improving health, well-being, and performance. We are a global team of Environmental Health and Safety (EHS) professionals working collectively within the company to make a positive difference in health care and have a deep sense of responsibility towards our customers, animals, society, and our planet. We have a site leadership role in our EHS organization available which is accountable for all EHS program execution and compliance at our Manufacturing Division's vaccine manufacturing facility in Durham, North Carolina. The Durham EHS Lead influences site leadership...

At the heart of innovation, our Regulatory Affairs team plays a vital role in delivering new medical advancements to patients around the world. By facilitating seamless communication and establishing robust procedures, we ensure swift, organized compliance with global regulatory agencies. As an international network on the leading edge of healthcare, we bring safe, reliable, and compliant medical products, practices, and solutions to the global market. Position Overview The Global Regulatory Liaison is responsible for developing and implementing worldwide regulatory strategies for assigned projects within the Oncology, Immunology, and Devices therapeutic areas. Acting as the single, accountable global point of contact,...

Translational Molecular Biomarkers is responsible for translating preclinical molecular biomarkers to clinical development across all therapeutic areas and all phases of clinical development at our company's Research Laboratories. Translational Molecular Biomarkers laboratories leverage a diverse array of technologies to develop biomarker assays to help confirm engagement of therapeutic targets and understand mechanisms of drug action and patient response. The Molecular Pathology group within the Translational Molecular Biomarkers organization is seeking a highly motivated and experienced Anatomic Pathologist (MD) for the role of Principal Scientist (Director) to join our innovative team. This position will play a crucial role in the supporting...

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

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

The Executive Director, Scientific Affairs (EDSA) maximizes meaningful bi-directional scientific exchange with the worldwide clinical and academic community to positively impact Research and Development (R&D) strategy for new medicines and to improve outcomes for patients. The EDSA leads a large investigator-initiated studies program in partnership with late-stage development teams in Medical Affairs while also supporting early-stage development teams. The role also partners with Medical Affairs leadership to develop the global Value Evidence And Medical (VEAM) Planning strategy across designated therapeutic areas. The EDSA has a key role at major Congresses, including, but not limited to, facilitating daily debriefs, engaging with...

The Discovery Pharmaceutical Sciences (DPS) group based in South San Francisco, CA is seeking an Associate Principal Scientist with biologics developability/manufacturability experience. DPS is a multi-disciplinary research group that provides drug delivery, solid state crystal form characterization, formulation support and small molecule and biologics developability assessments at the development and drug discovery interface. Our team is responsible for the characterization of pre-clinical drug candidates' physicochemical properties. We aim to work with partner groups to select candidates with optimal development properties while balancing all other key therapeutic properties. Our research also covers identification of preclinical formulations for pharmacology and toxicology studies...

We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an , committed to fostering an inclusive and diverse workplace. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global...

Supervisor, Environmental and Life Safety Role Join our dedicated team of fire, life safety, and environmental professionals. We take pride in keeping all our fellow employees on our Rahway, NJ campus safe and in maintaining the site's storm water, wastewater and hazardous waste compliance with all local and state regulations. Responsibilities The Environmental Life Safety Supervisor position is a 12 hour rotating shift. The Environmental Life Safety team monitors environmental and life safety systems for the site on a 24 hour, 7 day basis. The candidate that accepts the position is expected to work nights , weekends, and holidays...

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

The Analytical Research & Development, Cell Based Sciences in Rahway, NJ is seeking a motivated senior level scientist with extensive experience in biologics potency assays. More specifically, the ideal candidate will be a recognized expert developing mechanism-of-action reflective potency assays for the development of therapeutic proteins, monoclonal antibodies, antibody-drug conjugates, and/or complex modality-based products. Key Responsibility Responsible for providing scientific leadership and mentoring, expertise, and creativity in defining potency strategies, method development and problem solving for complex projects across the large molecule portfolio. Oversight of developing MoA-reflective potency methods using innovative and state-of-the-art analytical techniques and approaches, and generation of...

Primary responsibilities are routine testing and verification of print and imaging of labels, product inserts, carton materials, foils, etc and their review / release to production. This includes proofs, first prints, and reprints and documentation in a GMP laboratory. Additional responsibilities include entering data into SAP, training to become proficient in drafting investigations, working directly with vendors to correct component deficiencies and improve vendor processes, updating standard operating procedures, trains and learns to coordinate launch activities around print activities around printed material, and approve artwork in our global LIMS system. Testing equipment utilized include but are not limited to Text...

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

Our Company's Finance department is committed to developing future Finance leaders through its Finance MBA internship experience , which is a 10-week program that provides experience through project assignments, exposure to senior leaders, and networking opportunities. Program Overview & Responsibilities Our Company's Finance department plays an integral role in supporting those who develop, produce and commercialize our products every day. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding...

Position Description Our company's Animal Health, a global, research-driven company that develops, manufactures, and markets a broad range of veterinary medicines and services, is seeking Analytical Development Scientists for our R&D facility in New Jersey. This Senior Scientist will support the progression of molecules from discovery throughout the development process, transforming drug candidates into marketed products for our company's Animal Health, a company whose products enable pets and people to enjoy their time together and help keep livestock healthy to ensure a safe, sustainable, and high-quality food supply. The professional in this position will Support the analytical development of high...

The Associate Director– Device Tech Transfer is a leadership role within the Device Development and Technology Organization. This position is responsible for providing strategic program leadership, technical expertise, and project management in the scale-up, development, commercialization, and transfer of medical devices and combination products, with a focus on autoinjectors, prefilled syringes, and other drug delivery systems. The Associate Director will collaborate with a team of engineers and technical staff to support global and site-specific projects, facilitate technology transfer, and drive product robustness for sustained launch in alignment with the company's business goals, and quality and regulatory compliance. Essential Duties and...

Role Summary The Associate Director, Global Medical Information , is a mid-level, headquarters-based role within V&I Global Medical and Scientific Affairs (GMSA), responsible for the US and global core functions of the GMI organization Medical Information, which includes handling of all US healthcare professional (HCP) inquiries and escalated complex global HCP inquiries as well as generating insights and analysis; Medical Review of promotional and non-promotional scientific materials; Medical Education and Training of internal stakeholders; and Compendia and Pathways Submissions The Associate Director, has an advanced educational background and reports into the Director, Team Lead, GMI or Director, GMI. The Associate...

Position 2nd Shift Senior Technician - Under the direction of a Utilities Engineering Manager Provide utilities maintenance support to all Utilities and Facilities equipment, processes and sub-systems. Takes appropriate action to correct operational maintenance problems. Accountable for carrying out the manufacturing division and site mission by assuring the quality of products and services are of the highest quality, optimal cost, and delivered on schedule. Accountable for continuous improvement in all aspects of the operation. Must be able to function in a team-based culture and operate in an empowered environment. Identifies and demonstrates a working knowledge of customers, suppliers and...

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

Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety First, Quality Always” mindset striving for continuous improvement. We work in the local plant connected to our global manufacturing network to ensure the highest quality of raw materials, intermediates and finished products. The shift supervisor is a critical position to ensure the overall success of operations. Working closely with operators, the supervisor leads, coaches & monitors their team to maximize productivity and achieve department objectives. Leads and develops people and ensures safety and environmental requirements. Collaborates with different departments as...

Essential Functions include, but are not limited to The Associate Director is an important Business and Operations Leader within the Integrated Process Team (IPT) at the Wilson, NC Packaging & Device Assembly Site, providing strategic and operational guidance to a team of professionals. Responsibilities for this position will include coordinating engineering activities in support of our operations and organizational objectives, providing vision and direction, along with application of structured problem solving tools for investigation, event resolution, and continuous improvement. In addition, the position will be accountable for various compliance related activities, including assumption of key roles within the quality management...

of the Job Our company's Animal Health is a leading animal health company with an exceptionally strong brand and reputation among beef and dairy producers, veterinarians, and nutritionists. The Senior Territory Representative is a key member of the field sales team and plays a critical role in supporting our company's customer centric business model. This position is responsible for working in a dairy account-based environment to understand and identify customer needs, by selling our company's Animal Health products, supporting pull-through activities relative to the customer strategy, and ensuring that our company's Animal Health is viewed as bringing value and technical...

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

DUTIES AND RESPONSIBILITIES Material Handling Remove completed pallets of product from production area to shipping warehouse Follow all established procedures, safety rules, and SOP’s for the area Ensure proper and safe operation of equipment (e.g, pallet jack, stretch wrapper, floor scrubber, etc.). Report any malfunctions to supervisor and/or maintenance supervisor Maintain empty pallet area in a neat and orderly fashion Act as safety observer Maintain housekeeping in all areas responsible for in a neat and orderly fashion Perform all other duties as assigned Shipping Prepare finished product for shipment. Utilize forklift to load pallets of product on trucks or containers....

DUTIES Develop data standards, tools, and automated workflows to ensure high quality datasets, enable rapid data visualization, and optimize novel pharmacometric analysis and reporting workflows. Collaborate with Quantitative Pharmacology & Pharmacometrics (QP2) scientists and key partners, such as bioanalytical sciences, statistics, statistical programming, and clinical data management, across therapeutic areas to drive delivery of high-quality datasets. Monitor the flow of data between complex clinical data systems and the processes surrounding that data, drive creation of new data standards to enable analysis and workflow automation and implement new data initiatives (e.g. digital data). Obtain feedback from QP2 scientists and utilize this...

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

This individual contributor role, with moderate oversight, will have responsibility for processing the transactional activities associated with executing in vivo and in vitro studies at external CROs or collaborators and facilitating in-sourced scientific services in support of Discovery, Pre-Clinical and Translational Medicine (DPTM). This cross-functional support position will be directly accountable to the broader DPTM Operations team, and interface with Our Research & Development Division benchtop Scientists and External Scientific Leads, Finance, and Procurement to ensure that Purchase Orders (POs) are generated to initiate external work, and that invoices are reconciled for payment in a policy-compliant manner. The responsibilities of...

Manage the administrative and member service activities of the credit union. This includes overseeing and directing the activities of all branch offices and all member touchpoints. Ensure that quality member service is delivered to all members and that all credit union products and services are promoted similarly across all branches. Duties include, but are not limited to Create, or assist in the creation of, policies and procedures for the member service function. Ensure that policies and procedures reflect external rules and regulations and are communicated to and implemented by, all staff. Respond to technical and operational questions or problems from...

The Analytical Commercialization Technology (ACT) department within Analytical Chemistry in Development and Supply (ACDS) is seeking an applicant for a Senior Scientist position available at the West Point, PA site in the small molecule drug product Preliminary Stability Study testing laboratory. The successful candidate will utilize analytical characterization technologies and compliance principles to drive method robustness and high-quality stability data in support of late-stage pharmaceutical drug product development and commercialization. The Senior Scientist responsibilities include, but are not limited to, stability sample analysis, leading analytical investigations in a cGMP environment, implementing new technology or continuous improvement measures for optimized laboratory...

The Anatomic Pathology Group at our Company's South San Francisco site is seeking a passionate and talented Associate Principal Scientist with experience in bioinformatics and statistics to solve biological problems. The successful candidate will join a dynamic digital and quantitative multi-omics department to perform quantitative and statistical analysis on large-scale datasets to support novel drug and biomarker development. Key Responsibilities This is an individual contributor role as a subject matter expert responsible to implement data analytical tools and apply rigorous statistical methodologies to transform complex biomarker data into insights that can be readily used in drug development. Develop end-to-end data...

Associate Director, Discovery Portfolio Management, GPAM (P4) Global Project and Alliance Management (GPAM) sits in the R&D organization in our Research & Development Division . The Project Managers and Alliance Managers in GPAM are core members of discovery, development, and alliance teams. Project Managers drive these cross-functional teams to deliver projects and products that improve human health and our Company's business, and Alliance Managers ensure successful collaborations with our R&D alliance partners. The GPAM Project Management Office (PMO) is responsible for the development, sustainment, and training of GPAM-owned systems, tools, and business processes as well as alignment with Finance, IT,...

The Translational Sciences & Outsourcing group in the department of Pharmacokinetics, Dynamics, Metabolism and Bioanalytics (PDMB) is seeking a Senior Director to lead the regulated vaccine assay outsourcing (OS) team. The OS function within PDMB is responsible for the oversight of contract research organization (CRO) regulated preclinical/clinical assay method development, qualification/validation, and testing in support of Our Company’s vaccine programs. The Senior Director is a leadership position responsible for the strategic vision, oversight and operational excellence for vaccine bioanalytical outsourcing, ensuring alignment with corporate objectives and regulatory requirements. The Senior Director will oversee a multidisciplinary team of scientists in the...

We zijn op zoek naar een leidinggevende met oog voor gedrag én resultaten. Je weet mensen te ontwikkelen met een competentiegerichte aanpak. Door je pragmatische stijl die gericht is op continue verbetering van mens én proces begeleid je de professionalisering en output van ons productieteam. Je weet het hoofd koel te houden in onze door stevige groei gekenmerkte productieomgeving. Voor onze locatie in De Bilt zoeken wij een Team Lead Productie Welkom in ons team Onze productielocatie in De Bilt maakt deel uit van de Animal Health-divisie, waar we vaccins voor kippen produceren voor meer dan 100 landen wereldwijd. Met...

We zijn op zoek naar een leidinggevende met oog voor gedrag én resultaten. Je weet mensen te ontwikkelen met een competentiegerichte aanpak. Door je pragmatische stijl die gericht is op continue verbetering van mens én proces begeleid je de professionalisering en output van ons productieteam. Je weet het hoofd koel te houden in onze door stevige groei gekenmerkte productieomgeving. Voor onze locatie in De Bilt zoeken wij een Junior Operations Manager Welkom in ons team Onze productielocatie in De Bilt maakt deel uit van de Animal Health-divisie, waar we vaccins voor kippen produceren voor meer dan 100 landen wereldwijd. Met...

The Analytical Commercialization Technology (ACT) department within Analytical Chemistry in Development and Supply (ACDS) is seeking an applicant for an Associate Principal Scientist position available at the West Point, PA site in the small molecule drug product Preliminary Stability Study testing laboratory. The successful candidate will utilize analytical characterization technologies and compliance principles to drive method robustness and high-quality stability data in support of late-stage pharmaceutical drug product development and commercialization. The Associate Principal Scientist responsibilities include, but are not limited to, stability sample analysis, leading analytical investigations in a cGMP environment, implementing new technology or continuous improvement measures for...

This position resides within our company's Value and Implementation (V&I), Outcomes Research organization, which is responsible for real-world evidence generation and outcomes research to enable sustained patient access to our company’s innovations and improve patient health outcomes. Under the guidance of a senior leader, this individual will support the V&I, Outcomes Research teams in Hematology with a primary focus on lymphomas. Primary Responsibilities Support the value evidence teams in hematology and lead the execution of value evidence projects in lymphomas for in-line and pipeline products. Provide outcomes research leadership on cross-functional regional and global teams. Critically assess drivers and barriers...

Role Summary The Regional Medical Scientific Director (RMSD) is a credentialed (i.e., PhD, PharmD, DNP, MD) therapeutic and disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs). This MSL type role provides balanced, factual, scientific information about non-product areas of interest to the Company and replies to scientific questions from SLs, including questions about Company products. The work of an RMSD is aligned to Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights. RMSDs liaise between the scientific community and the Company to enhance the comprehension of scientific foundations and goals for approved,...

Position This position will lead the Maintenance team for execution of day-to-day repair and maintenance activities, preventative and proactive maintenance initiatives, and provide support for site Environmental Health and Safety (EHS) and regulatory compliance. Strong interpersonal and leadership skills and the ability to work closely with Operations, Research & Development, Animal Care, Quality, Environmental Health and Safety, and engineering are key components of this position. Maintenance Manager Responsibilities Plan, Staff, and Oversee operations of maintenance and utilities for biotech manufacturing, Quality Control, Research & Development, Animal Research, and all other support functions on the De Soto Campus. Limited responsibilities...

Company Overview Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety First, Quality Always” mindset striving for continuous improvement. We work in the local plant connected to our global manufacturing network to ensure the highest quality of raw materials, intermediates and finished products. The Specialist Manufacturing Automation Engineer in the West Point Digital Manufacturing Operations organization will be responsible for the manufacturing process automation systems in the Barrier Operations Formulation and Filling facility at the West Point, PA site. The candidate will provide day to day support functions...

Reporting into the Director, Logistics and Distribution Technology the Associate Director, Logistics and Distribution Technology will be responsible and accountable for subject matter expert technical support for distribution and logistics of human health Drug Substance, Drug Product and Finished Goods globally. The Packaging Technical Operations organization aims to be an industry leader in problem-solving, delivering robust and pragmatic technical solutions to accelerate the commercialization of new products, and ensuring an uninterrupted, compliant supply of commercialized products for the benefit of patients. The Logistics and Distribution Technology Director is integral to this mission. The successful candidate will possess deep technical expertise,...

The Clinical Specialist Position is a combined position of clinical scientist and study management duties supporting one or more clinical trials. Under the oversight of a clinical scientist, study manager, or program lead, the Clinical Specialist may be responsible for but not limited to Responsibilities Maintain clinical trial files (including eTMF), project processes, tracking systems, and other utilized study or departmental systems Generating and reviewing medical monitoring reports Creating and maintaining project schedules Distributing, reconciling and archiving clinical documents Tracking and reconciling labs/samples May interact with internal and external stakeholders (e.g. study sites, committees) in support of clinical trial objectives...

The Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the Atherosclerosis section of the Atherosclerosis & Metabolism therapeutic area. Our company's Atherosclerosis & Metabolism medicines span all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle of late-stage clinical development and studies, including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. Specifically, the Senior Director May Be Responsible For Evaluating pre-clinical and translational work for the purpose of generating early clinical development plans and Investigational New...

Our Animal Health Manufacturing 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. Your main field of attention is to provide technical support to Vaccine and Biopharmaceutical Manufacturing for commercial Animal Health products. The focus of an Sr. Specialist within the Regional Projects team in the BioTechnology Solutions (BTS) department is on Vaccine process evaluations/transfers in support of commercial antigen manufacturing and sterile fill-finish to produce liquid or lyophilized products. Within a multidisciplinary environment you will cooperate with your colleagues from BTS-Process Development, BTS-Site...

Role Summary The Regional Medical Scientific Director (RMSD) is a credentialed (i.e., PhD, PharmD, DNP, MD) therapeutic and disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs). This MSL type role provides balanced, factual, scientific information about non-product areas of interest to the Company and replies to scientific questions from SLs, including questions about Company products. The work of an RMSD is aligned to Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights. RMSDs liaise between the scientific community and the Company to enhance the comprehension of scientific foundations and goals for approved,...

As a member of the Utility and Energy Operations team, the Medium Voltage Engineering Manager (MVEM) will support the Rahway Campus as the medium voltage (1KV – 69KV) subject matter expert. The MVEM will ensure safe and reliable design, operation, and maintenance of all medium voltage electrical equipment. The MVE will also be responsible for executing utility and energy projects, maintaining system design basis, troubleshooting systems nonconformances, and supporting medium and long-range utility planning. We are seeking a self-motivated, independent engineer with strong analytical and problem-solving skills to provide engineering support for our campus facilities. The successful candidate will pay...

The U.S. Oncology business is a growing and dynamic part of our company. We are currently seeking qualified candidates for the role of Director, U.S. Oncology Marketing (TROP2 ADC) – Gynecological Cancers . This role is focused on the commercialization of an investigational TROP2-directed antibody-drug conjugate currently in Phase III clinical development in multiple tumor types. The clinical program is broad with studies in across a range of tumor types including gynecological, lung, GI, bladder, and breast cancers. The product is being jointly developed. The first expected U.S. launch is in endometrial cancer. We are seeking an experienced and strategic...

We are seeking a highly motivated individual for the role of Associate Director Engineering - MDCP Technical Lead, supporting the Wilson Packaging Technical Operations Team. This role will serve as the primary medical device and combination product (MDCP) point of contact for the site Packaging Technical Operations team. The MDCP Technical Lead will have responsibilities for supporting the design/tech transfer and sustainment activities of MDCPs at the Wilson site and ownership for various MDCP-related QMS topics to ensure compliant implementation and robust application at the site. Experience in design controls, device risk management, medical device, combination products, prefilled syringes, autoinjectors,...

Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety First, Quality Always” mindset striving for continuous improvement. We work in the local plant linked to our global manufacturing network to ensure the highest quality of raw materials, intermediates, and finished products. Position 3rd Shift Senior Utilities Technician - Under the direction of a Utilities Engineering Manager Provide utility maintenance support to all Utilities and Facilities equipment, processes and sub-systems. Takes appropriate action to correct operational maintenance problems. Accountable for carrying out the manufacturing division and site mission by...

We are seeking a highly motivated individual for the role of Associate Director, Tech Transfer Leader supporting the Wilson Packaging Technical Operations Team. This role will drive end-to-end technical readiness for new product introduction and technology transfer at the site, including management of all activities required for the technical transfer of new and in-line products and processes. The incumbent will have broad, experience-based skillsets in Technology Transfers with key focus on standards, technical robustness, and right first-time success for commercial scale device assembly and packaging technology and components. Experience also includes strong project management skills and utilization of program/portfolio management...

Role Summary The Regional Medical Scientific Director is a credentialed (i.e., PhD, PharmD, DNP, MD) therapeutic and disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs). This MSL type role provides balanced, factual, scientific information about non-product areas of interest to the Company and replies to scientific questions from SLs, including questions about Company products. The work of an Regional Medical Scientific Director is aligned to Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights. Regional Medical Scientific Director liaise between the scientific community and the Company to enhance the comprehension of scientific...

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

Join our Global Animal Health Manufacturing (GAHM) Biotechnology Solutions (BTS) team as a leading scientific Commercial Lyophilization (Freeze Drying) expert! The Technical Lead, Lyophilization/ Fill-Finish will provide guidance, recommendations and judgment for strategic technical issues and decisions pertaining to the following domains – commercial freeze drying (lyophilization) and fill-finish. The Technical Lead will ensure a robust first principles-based tech-transfer and scale-up of lyophilization while working cross functionally with our Animal Health Large Molecule strategy team, regional operations team and engineering teams involved in capital investment, technology transfer, and operational readiness to ensure scientific rigor. Responsibilities Build and maintain strong and...

The Associate Director, Global Category Lead is responsible for all Procurement related activities supporting the strategic analysis of suppliers, supply markets, and supply chains within the Global Medical & Scientific Affairs (GMSA) area of the Research & Development Sourcing & Procurement organization. This role will take an active leadership role in the development of procurement strategies, global category management, process improvement, contract management, risk management, stakeholder management and supplier value management within this category. The selected candidate will be responsible for ensuring that all sourcing strategies are compliant and follow Global Procurements’ Sourcing Management Process (SMP) and will prepare and...

The West Point, PA site is our Company’s largest vaccine manufacturing facility that manufactures bulk and final dosage forms for our vaccine products and is growing to meet future demand . Our company’s pro duction s ystem , MPS , is an integrated production system for how we design, manage, and continuously improve our operations and supporting business processes, enabled through the development of our people. The West Point Site MPS Team is responsible for driving MPS throughout the organization to enable change in the operating systems, management systems, and mindsets, behaviors , and capabilities of our people to manufacture...

Our Sr. Account Managers interact face to face with veterinarians, nutritionists, producers, university professionals, sales representatives and marketing to understand their needs and consult to offer the right solutions. We work collaboratively with Field Sales Teams and play a critical role in supporting our customer centric business model. This position is responsible for providing technical support to Sales and Marketing for Animal Health products (biologics, pharmaceuticals and animal monitoring) specific to the US beef cattle business. Responsibilities include providing technical support for Ruminant products and programs, including response to product inquiries and adverse reports in accordance with internal, FDA, CFIA...

Are you looking for an exciting opportunity with a rapidly growing pharmaceutical manufacturer? If so, this is the opportunity for you! 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. At our Company's campus in Elkton, Virginia, we have an entry level position available to support and sustain our manufacturing processes. The manufacturing facility is located in the Shenandoah Valley along the Shenandoah River and the Blue Ridge Mountains a short distance from the University of Virginia and...

Our Research & Development Division in South San Francisco, a wholly owned subsidiary of our Company, is focused on driving discovery research. Our new multi-disciplinary discovery research site offers state-of- the-art resources to explore the most promising science combined with our Company’s world-class R&D expertise in small molecules and biologics. Located within the heart of the Bay area’s biomedical community, research conducted in our new laboratories spans exploratory biology through early clinical development and is an integral part of our Company’s powerful world-class network of drug and vaccine discovery. At our Company, we are inspired by the belief that a...

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...

We're seeking an exceptional leader to join our team as an Associate Director, Engineering, Maintenance & Utilities. As a leader in our team, you'll have the opportunity to make a significant impact on our operations and drive business results. As a member of the Engineering, Maintenance, & Utility Department, the Associate Director is accountable for the management of maintenance or reliability engineers supporting a defined manufacturing area. This group is responsible for improving asset reliability and manufacturing capacity by providing technical support in the field on engineering resolution of manufacturing mechanical or automation problems, processes incompliance with GMP, safety, and...

Our company has an exciting and growing Ophthalmology pipeline, reinforcing our position as a sustainable innovation engine for the coming decade. Our Global Market Access (GMAx) organization is driven by a passion to save and improve lives by ensuring sustainable access to our medicines and vaccines at a price reflective of their value. We work collaboratively across the enterprise, and with regional and local market teams, to deliver the development and implementation of integrated access strategies, excellence in pricing strategy and execution, and shaping of the external access landscape. We drive sustainable patient access through innovation in patient access models...

Reporting into the Executive Director Packaging Technical Operations the Director Packaging Distribution, Components and Systems Center of Excellence (COE) is responsible and accountable for technical leadership, strategic planning and portfolio execution of key work in support of Centers of Excellence for the packaging and device community including logistics and distribution technologies, small molecule bulk and primary packaging components and packaging master data and systems. The Packaging Technical Operations organization aims to be an industry leader in problem-solving, delivering robust and pragmatic technical solutions to accelerate the commercialization of new products, and ensuring an uninterrupted, compliant supply of commercialized products for...

Job Summary The Senior Specialist, Planning & Scheduling is responsible for managing and optimizing production planning and scheduling activities to ensure efficient product supply and meet site capacity requirements. This role involves cross-functional collaboration, data analysis, and leadership of a small planning team to maintain supply chain performance and support continuous improvement initiatives. Education Minimum Requirement Bachelor's of Science in Business or related field with 5+ years of related industry planning experience Bachelor's of Science in Business or related field with 3+ years of related industry planning experience and either APICs certification or Degree in Supply Chain Management or equivalent...

Reporting into the Director Packaging Platform Technical Leadership the Associate Director Medical Device and Combination Product (MDCP) Platform Packaging and Assembly Technical Leadership will be responsible and accountable for technical leadership, strategic planning and portfolio execution of key packaging and assembly platforms, with a focus on combination drug products such as prefilled syringes and autoinjectors. The Packaging Technical Operations organization aims to be an industry leader in problem-solving, delivering robust and pragmatic technical solutions to accelerate the commercialization of new products, and ensuring an uninterrupted, compliant supply of commercialized products for the benefit of patients. The Associate Director of MDCP...

Associate Director – Foreign Trade Zone The Associate Director FTZ will be a key Trade team member within the Logistics & Regions Org. of our Company's Research & Development Global Clinical Supply Chain. The core responsibilities are full ownership and accountability of several FTZ’s and spearheading future establishment of new FTZs as required . The ideal candidate will apply their FTZ exp ertise to proactively identify opportunities for use and align with the related enterprise-wide initiatives, ensuring no conflict in wider efforts and business strategies. High degree of proactivity and Trade compliance rigor is required . The successful candidate will...

Sr. Specialist Global Data Center Engineer We have an exciting new job opportunity and are looking to hire a Sr. Data Center Engineering Specialist. At our company, we are committed to delivering innovative health solutions that advance the prevention and treatment of diseases in people and animals. Join our Data Center Services Product Team and be part of a team that supports the delivery of Technology Space products and services globally. Responsibilities Support design and delivery of Technology Spaces for new builds, renovations, consolidations, relocations, migrations, and decommissions. Maintain active and direct interaction with customers and stakeholders to gather and...

Director, Packaging Shipping Systems (Logistics and Distribution Technology) Reporting into the Director Packaging Distribution, Components and Systems COE the Director, Logistics and Distribution Technology will be responsible and accountable for subject matter expert technical support for distribution and logistics of human health Drug Substance, Drug Product and Finished Goods globally. The Packaging Technical Operations organization aims to be an industry leader in problem-solving, delivering robust and pragmatic technical solutions to accelerate the commercialization of new products, and ensuring an uninterrupted, compliant supply of commercialized products for the benefit of patients. The Logistics and Distribution Technology Director is integral to this...

We are looking for dynamic individuals who thrive in a team environment and are driven to succeed. The Rare Disease Account Specialist serves as a key point of contact to customer accounts for our Company’s Pulmonary Arterial Hypertension (PAH) business. This role will be critical in establishing our presence in PAH and our commitment to supporting the efforts of PAH healthcare providers in improving patient health outcomes. This role will generate demand for our Company products, build and maintain a strong rapport with providers and office staff, engage and support account executives who help secure formulary access, and design account...

The Senior Director will report to an Associate Vice President in the Oncology Clinical Research Group. Under the guidance of a supervisor, the Senior Director has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our Oncology medicines span all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. Responsibilities Specifically, the Senior Director may be responsible for Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy...

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

Our Company's Discovery Immunology groups are developing a world class pipeline to treat immune mediated diseases across Gastroenterology, Rheumatology and Dermatology. We are seeking an exceptional scientific leader with deep expertise in Immunology Discovery to join our vibrant Research & Discovery team in San Diego in our journey to discover and develop the next generation of best-in-class medicines that will raise the therapeutic ceiling in the treatment of immune-driven diseases. This role will report to the Associate Vice President, Immunology Discovery. You will serve as Discovery Immunology Project lead on early-stage immunology programs, driving projects from scientific rationale for target...

We’re seeking an experienced Senior Scientist to join the Infectious Disease and Vaccines department at our research site in West Point, PA. The candidate will have a primary role on a team responsible for the discovery and development of novel antiviral treatments, with a particular focus on HIV. The candidate will independently design and execute experiments to interrogate fundamental virus biology, virus-host interactions, and immunological responses using various biochemical and cell-based assays and in vivo disease models. The candidate should have a strong background in virology, immunoassay and genomic technologies, cell biology, animal pharmacology, and general knowledge of infectious disease...

Senior Specialist, Manufacturing Automation (Rota POD IPT Lead) Responsible for working both as an integrated process team lead (IPT) and as a technical subject matter expert that will enable Our Company to deploy and operate a one-of-a-kind facility with a full end to end process consistent with global business processes, common global information, and IT supporting projects / application / technology suite. This position requires knowledge and experience in own discipline while still acquiring higher-level knowledge and skills. The position will build knowledge of the company, processes, clients/customers and will solve a range of problems while providing possible solutions. This...

The Biologics Operations Sourcing Associate Director in Global Operations Sourcing Procurement supports the sourcing and contracting of large molecules from commercialization through post NDA launch. The selected candidate will be responsible for the overall sourcing strategies supporting the large molecule biologics category. In addition, they will be developing and implementing, procurement strategy, Global Category Management, contract management, risk management, stakeholder management, and supplier value management within this category. Developing and maintaining strong relationships with key leaders and stakeholders, namely Commercialization, External Manufacturing, Quality, Regulatory, Supply Chain, Finance, Legal, Shared Business Services, and other corporate functions. Primary activities include, but are...

Dir, Engineering - Director, Assembly and Packaging Platform Technical Leadership Reporting into the Executive Director Packaging Technical Operations the Director Packaging and Assembly Platform Technical Leadership will be responsible and accountable for technical leadership, strategic planning and portfolio execution of key packaging and assembly platforms, with a focus on combination drug products such as prefilled syringes and autoinjectors. The Packaging Technical Operations organization aims to be an industry leader in problem-solving, delivering robust and pragmatic technical solutions to accelerate the commercialization of new products, and ensuring an uninterrupted, compliant supply of commercialized products for the benefit of patients. The Director...

Are you looking for an exciting opportunity with a rapidly growing pharmaceutical manufacturer? If so, then this is the opportunity for you! The Lead Maintenance and Instrumentation Technician is responsible for providing equipment troubleshooting and maintenance support for a new product feasibility project/manufacturing support. Support updates to standard operating procedures (SOP's) and preventative maintenance (PM's) plans, as requested. 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...

Position The Associate Director – International Tax will report directly to the Director, Tax Operations, located in Rahway, NJ Responsibilities will include, but not limited to Responsible for preparation and review of US international tax compliance forms and disclosures (Forms 5471, 8858, 8865, 1118, 8992, 8993) Responsible for US international tax calculations, including but not limited to Subpart F, GILTI, FDII, FTC, Assist with ASC 740 review, Assist with country-by-country reporting and filing of Form 8975 and Schedule A Ensure timely compliance with international requirements including FBAR and Pillar 2 reporting, Assist with cross-border structuring and planning to support...

Are you looking for an exciting opportunity with a rapidly growing pharmaceutical manufacturer? If so, then this is the opportunity for you! The Senior Instrumentation Technician is responsible for providing equipment troubleshooting and maintenance support for a new product feasibility project/manufacturing support. 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. Under the supervision of the Maintenance Manager and/or Lead, the selected candidate will...

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

Position Description This position is for a principal scientist in biostatistics. The candidate should have a solid knowledge of statistical methodology, experimental design, computing software and data management; a general understanding of worldwide regulatory requirements; and with good clinical trial experience in Phase II/ III trials. The knowledge must be sufficient to ensure that sound scientific principles and statistical methods applied to designing and analyzing clinical trials in support of worldwide regulatory submissions. This position involves interaction with Medical, Data Coordination, Statistical Programming, Research Laboratories scientists and Regulatory staffs in designing and analyzing clinical trials and coordinating the statistical activities...

Are you looking for an exciting opportunity with a rapidly growing pharmaceutical manufacturer? If so, then this is the opportunity for you! Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety First, Quality Always” mindset striving for continuous improvement. We work in the local plant connected to our global manufacturing network to ensure the highest quality of raw materials, intermediates, and finished products. The Sr. Specialist, Calibration Engineer is a member of the Engineering, Maintenance and Site Services (EMSS) team providing support to the Durham Bulk Facility. The successful...

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

We have an exciting opportunity for a Senior Specialist to join the business support and project management 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 requires the ability to work independently with minimal supervision, produce/complete various assignments requiring analytical ability, demonstrate independent judgment, creativity and problem-solving skills. This role also requires strong collaboration and communication skills to enable interfacing with both internal contacts (local site level) and external contacts (external customers, above site partners,...

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 sites to our Manufacturing Division -Wilson. The...

Position Description The Formulation, Laboratory, and Experimentation (FLEx) Center is a new multi-modality (small molecule, biologics, vaccine) Drug Product development and Good Manufacturing Practice (GMP) clinical manufacturing plant in Rahway, New Jersey. The Sterile Production Supervisor manages a team of technicians for daily operations that support sterile supply, aseptic formulation, aseptic filling, and visual inspection. This role require adherence to GMP procedures, strong attention to detail in completing GMP documentation, proficiency in electronic systems, and participation in continuous improvement projects. Positions may also support commissioning, qualification, and demonstration of new equipment and technologies. Successful candidates will collaborate closely with team...

We are currently seeking a motivated Principal Scientist (Robotics/Automation) to join the Translational Sciences and Outsourcing group at our West Point/Springhouse, PA location within the department of Pharmacokinetics, Dynamics, Metabolism and Bioanalytics (PDMB). This role will focus on translating scientific research into practical applications by delivering and implementing laboratory automation solutions on robotic platforms. Responsibilities include engaging in cross-functional, end-to-end process development involving close collaboration between scientific and IT teams. The candidate will possess direct experience in designing, developing, and transferring automated ADME (absorption, distribution, metabolism, and excretion) and bioanalytical assays. They must demonstrate the ability to execute these assays...

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

The Development and Commercialization Team (DCT) leader is accountable for delivering a fully integrated stage-appropriate CMC development and commercialization strategy which yields the target commercial product. The specific role will be responsible for advancing the company's biologics portfolio. Correspondingly, the DCT leader will be responsible for delivering world class outcomes in the following areas Responsible for on-time, end-to end execution of DCT deliverables including – robust processes & analytics, an integrated control strategy, successful tech transfer packages, filing and approval, and a robust commercial supply chain to achieve uninterrupted long-term supply Lead DCT. Critically assesses all team deliverables & fosters...

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

We're seeking an exceptional leader to join our team as an Associate Director, Engineering, Maintenance & Utilities. As a leader in our team, you'll have the opportunity to make a significant impact on our operations and drive business results. As a member of the Engineering, Maintenance, & Utility Department, the HEPA Certification Associate Director is accountable for the management of the HEPA certification personnel and program supporting our Manufacturing Division at the West Point, PA site. This group is responsible for improving asset reliability and manufacturing capacity by providing technical support in the field on engineering resolution of manufacturing mechanical...

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

The Director reports to the Executive Director of SMAR&D and will lead a team of approximately 10-15 analytical scientists in Rahway that works closely within multidisciplinary DSCS teams. This role has a wide responsibility for analytical method development and testing for chemical and biocatalytic synthetic processes, and / or a variety of formulations (e.g., oral, parenteral, and specialty dosage). The director should be well engaged with regulatory and industry trends to guide future activities for Analytical R&D and DSCS. The candidate will have experience in an innovative analytical/regulatory/GMP environment. The Director will effectively partner with the SMAR&D leadership team in...

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

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

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

Are you passionate about improving healthcare outcomes and enhancing consumer experiences? We are seeking a dynamic and results-driven Healthcare Consumer Activation Manager to join our innovative team. In this role, you will play a pivotal part in shaping our consumer engagement strategies, promoting health awareness, and ensuring that our consumer solutions meet the evolving needs of people, patients, and healthcare professionals alike. As a key member of our organization, you will collaborate within cross-functional teams to develop and implement effective marketing initiatives, analyze market trends, and leverage consumer insights to inform decision-making. If you are a strategic thinker with a...

Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety First, Quality Always” mindset striving for continuous improvement. We work in the local plant linked to our global manufacturing network to ensure the highest quality of raw materials, intermediates, and finished products. The Senior Maintenance Technician will be a member of the Maintenance & Operations team within the Vaccines integrated process team for a start-up vaccine manufacturing facility in Wilson, NC. This person is accountable for executing shop floor operations as well as providing preventative/corrective maintenance on primary filling, inspection,...

The Global Medical Excellence Director (GMED) reports to the Sr. Director, Global Medical Excellence, and is an experienced leader/subject matter expert (SME) in General and Specialty Medicine. The GMED is responsible for overseeing and driving Value & Implementation (V&I) General & Specialty Medicine Therapeutic Area (TA) medical excellence initiatives. The role entails developing and implementing strategies to enhance Medical Affairs operations, coordination across multiple functions, ensuring the highest scientific standards, and increasing the effectiveness of Medical Affairs planning. The GMED provides strategic and operational leadership in the achievement of our Medical Affairs global strategies, serving as part of the Global...

Under the guidance of a senior leader, the Principal Scientist (Director), Outcomes Research—Women’s Cancer will be a member of the overall team responsible for an asset-level strategy and plan. Will develop and maintain tumor and indication expertise relevant to the asset. Will assess unmet medical need and value across tumors/indications for the asset for asset-level tumor/indication prioritization discussions. Types of studies executed include prospective and retrospective observational studies to characterize disease burden and epidemiology, treatment patterns, healthcare resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, and systematic reviews and meta-analyses. Incumbent is expected...

Our Engineers support internal and external manufacturing operations to remain operational, continuously improve and innovate. With our extensive range of facilities and environments, our Engineers have opportunities across many diverse areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation. Summary, Focus and Purpose The Vaccines Technology Specialist position is responsible for providing technical support to primary filling, inspection, and/or packaging operations within the vaccine manufacturing facility at the Wilson, NC Site. This position will be an individual contributor and member of the Technical Operations Team within the Rota-POD Integrated Process Team. This is...

The Executive Director of Global Auditing will report to the Head of Global Quality Compliance Support. The responsibility of this position crosses Human and Animal Health operating units and requires extensive collaboration with manufacturing sites, contractors, and suppliers. Primary Responsibilities Lead global team of GxP auditing experts to ensure our company’s manufacturing sites, contractors, and suppliers adhere to the highest quality and compliance standards Develop and maintain global Quality Management System (QMS) documents pertaining to auditing and inspections; ensure team and company adherence to these documents Develop a risk-based audit schedule for our company’s auditable entities and ensure schedule adherence...

The Sr. Specialist of Biosafety is accountable for providing and managing an efficient and effective Biosafety program at the Millsboro, Delaware Animal Health site. The successful candidate will play a key role in developing, implementing, and maintaining biosafety programs and policies to ensure a safe working environment in compliance with local, state, and federal regulations. The Sr. Specalist of Biosafety will collaborate with various departments to promote best practices in biosafety and manage risk assessments related to small scale biological activities, large scale vaccine manufacture, and animal studies. This position sits within the Global Safety & Environment organization, and reports...

Duties and Responsibilities Respond and assists in recovery and repair of utilities and production equipment. Troubleshoot failed electrical, mechanical, hydraulic & pneumatic components utilizing basic and advanced problem-solving techniques, will require knowledge of various levels of test equipment up to and including predictive maintenance tools. Complete assigned preventative maintenance actions utilizing developed standards as prescribed by OEM and engineering specifications, includes minor and major overhauls, calibration, detailed inspections, and basic cleaning and lubricating. Complete basic and advanced corrective action repairs supporting safety, quality, and equipment reliability. Perform tolerance specific fabrication tasks utilizing shop equipment such as mills, lathes, drill press,...

Associate Director, Portfolio & Program Management (PPM) The Associate Director in Regulatory Planning and Publishing works closely with various stakeholders to drive the identification, planning, execution, and management of activities that deliver high quality and timely regulatory and safety submissions for approval. The incumbent will be responsible for translation of regulatory strategy into an execution plan and is expected to have excellent project management skills with a strong track record of demonstrated leadership on cross-functional regulatory teams. Should be capable of independent management of all submission projects and documents, at any level of complexity, across all submission types throughout the...