Quality Systems Jobs in Rahway, NJ

Job DescriptionReporting to the AVP of New Modalities Manufacturing Division Quality this leader is responsible for providing Antibody Drug Conjugate (ADC) expertise and supporting a quality oversight model necessary to facilitate agility and speed-to-market while ensuring sustained compliant supply...

Job DescriptionJob Title: Compliance Engineer FLEx Sterile OperationsLocation: Rahway New JerseyReports to: FLEx Sterile Compliance Lead Pharmaceutical Operations & Clinical SupplyJob Description:The Formulation Laboratory and Experimentation (FLEx) Center in Rahway New Jersey features a cutting-ed...

Job DescriptionJob DescriptionThe Small Scale Organics (SSO) Pilot Plant is a Good Manufacturing Practices (GMP) facility within the Process Research and Development (PR&D) organization which enables gain of critical internal experience during scale-up of clinical supplies manufacturing demonstratio...

Job DescriptionJob Description:The Formulation Laboratory and Experimentation (FLEx) Center in Rahway New Jersey features a cutting-edge sterile drug product cGMP clinical supply manufacturing facility known as FLEx Sterile which is currently in the operational startup phase. The FLEx Sterile facili...

Job DescriptionThe Director Quality Assurance will be responsible for team leadership and technical subject matter expertise in Sterile Drug Product Quality Operations at our Companys Rahway New Jersey site. This position will serve a critical role in supporting the expansion of clinical development...

Job DescriptionThe Biologics Process Research & Development organization within our Company Research Labs is responsible for developing the drug substance manufacturing processes for our Companys biologics pipeline. We work closely with colleagues in Discovery Pre-clinical and Early Development to r...

Job DescriptionThe Human Factors director plays a pivotal role in combination product development (both design and process) commercialization and lifecycle management. This person leads the Human Factors team to perform and manage human factors activities to ensure compliance with US and global regu...

Job DescriptionThe Ethics & Compliance Office (ECO) is accountable for our Companys ethics and compliance program. Reporting to the Director ECO Corruption Data Risk Monitoring Program the Senior Specialist will be part of a U.S.-based headquarters compliance team and play a key role in compliance r...

Job DescriptionOur Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance we ensure the safety and efficacy of our existing and pipeline products to produce safe effective innovative medicine.To...

Job DescriptionThe Formulation Laboratory and Experimentation (FLEx) Center is a new multi-modality (small molecule biologics vaccine) Drug Product development and Good Manufacturing Practice (GMP) clinical supply manufacturing facility in Rahway New Jersey.The Second Shift Sterile Process Engineer...

Job DescriptionThe Rahway FLEx (Formulation Laboratory & Experimentation) Center is a flexible agile facility that brings together capabilities operations and talent to accelerate the pipeline.Pharmaceutical Operations & Clinical Supply is seeking applicants for a Manufacturing Engineering Lead to s...

Job DescriptionThe Rahway FLEx (Formulation Laboratory & Experimentation) Center is a flexible agile facility that brings together capabilities operations and talent to accelerate the pipelinePharmaceutical Operations & Clinical Supply is seeking applicants for a Manufacturing Engineering Lead to su...

Job DescriptionThe Biologics Process Research & Development organization within our Company Research Labs is responsible for developing the drug substance manufacturing processes for our Companys biologics pipeline. We work closely with colleagues in Discovery Pre-clinical and Early Development to r...

Job DescriptionThe Biologics Process Research & Development organization within our Company Research Labs is responsible for developing the drug substance manufacturing processes for our Companys biologics pipeline. We work closely with colleagues in Discovery Pre-clinical and Early Development to r...

Job DescriptionRole SummaryThe Associate Director Medical Operations (AD MO) is a role within Value and Implementation Global Medical and Value Capabilities (V&I GMVC) in Value and Implementation (V&I) that reports directly to the Director Medical Operations Lead.The AD MO is an integral member of t...

Job DescriptionIn partnership with the Clinical Quality Operations Lead (CQOL and Head of CQO the CQOM is accountable for the execution of operational quality activities within the assigned therapeutic area. This includes operational quality management and inspection management activities.The CQOM w...

Job DescriptionOur Research & Development Division Quality Assurance (QA) is an independent organization that provides quality focus at each critical stage of the product development life cycle including post approval marketing to ensure high-quality safe and effective products contributing to the c...

Job DescriptionAssociate Principal Scientist Device Technical and Engineering Lead (Associate Director Equivalent)Our companys Device Product & Process Development (DPPD) Team designs develops and commercializes novel biologic/drug/vaccine - device enabled combination products to achieve safe and e...

Job DescriptionAssociate Principal Scientist Device Technical and Engineering Lead (Associate Director Equivalent)Our companys Device Product & Process Development (DPPD) Team designs develops and commercializes novel biologic/drug/vaccine - device enabled combination products to achieve safe and e...

Job DescriptionPrincipal Scientist Device Technical and Engineering Lead (Director Equivalent)Our companys Device Product & Process Development (DPPD) Team designs develops and commercializes novel biologic/drug/vaccine - device enabled combination products to achieve safe and effective delivery to...