Regulatory Affairs Jobs in Rahway, NJ

Job DescriptionThe Senior Clinical Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Oncology therapeutic area specifically in our Hematology Section. Our companys Oncology medicines spa...

Job DescriptionThe Senior Clinical Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Oncology therapeutic area specifically in our Hematology Section. Our companys Oncology medicines spa...

Job DescriptionThe Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Oncology therapeutic area specifically in our Hematology Section. Our companys Oncology medicines span all phases o...

Job DescriptionThe Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Oncology therapeutic area specifically in our Hematology Section. Our companys Oncology medicines span all phases o...

Job DescriptionThe Executive Director has primary responsibility for the planning and directing clinical research activities involving new or marketed drugs for oncology indications. The Executive Director will manage and oversee the entire cycle of clinical development including study design initia...

Job DescriptionThe Executive Director (Distinguished Scientist) and Product Development Team (PDT) lead has primary responsibility for the planning and directing of clinical research activities involving new or marketed medicines in the Oncology therapeutic area Hematology section.The Executive Dire...

Job DescriptionThe Executive Director (Distinguished Scientist) and Product Development Team (PDT) lead has primary responsibility for the planning and directing of clinical research activities involving new or marketed medicines in the Oncology therapeutic area Hematology section.The Executive Dire...

Job DescriptionOur Regulatory Affairs team in General Medicine advances medical innovation to patients by establishing clear timely and robust strategies for registration enabled by engagement with global health authorities. We work across functions and geographies to advance development programs an...

Job DescriptionOur company is a global health care leader with a diversified portfolio of prescription medicines vaccines and animal health products. Today we are building a new kind of healthcare company one that is ready to help create a healthier future for all of us. Our ability to excel depends...

Job DescriptionScientist (R2) BioassayNorth American GMP Operations Rahway NJWe invite individuals who possess a deep passion for promoting lifesaving and life-enhancing products to join our dynamic team. Our team is highly dedicated and committed to offering exceptional scientific oversight driving...

Job DescriptionThe Senior Clinical Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new medicines in the Oncology Asset therapeutic area. Our companys Oncology Asset TA medicines are generally in transition from early...

Job DescriptionPosition title Associate Director Global Marketing Swine Technical NutritionistOrganizational unitAnimal Health Global Marketing - SwineSummary of the jobThe Global Marketing Swine Technical Nutritionist is a senior technical role within our companys Animal Healths Global Swine Busin...

Job DescriptionThe Executive Director Chemistry Manufacturing Control for Biologics (Biologics-CMC) is accountable for managing a team of CMC professionals and ensuring rigor in CMC regulatory strategy as well as delivery of high quality CMC submissions for late phase new modality biologics products...

Job DescriptionThe Executive Director Chemistry Manufacturing Control for Biologics (Biologics-CMC) is accountable for managing a team of CMC professionals and ensuring rigor in CMC regulatory strategy as well as delivery of high quality CMC submissions for late phase new modality biologics products...

Job DescriptionOur Regulatory Affairs team in General Medicine advances medical innovation to patients by establishing clear timely and robust strategies for registration enabled by engagement with global health authorities. We work across functions and geographies to advance development programs an...

Job DescriptionOur Regulatory Affairs team in General Medicine advances medical innovation to patients by establishing clear timely and robust strategies for registration enabled by engagement with global health authorities. We work across functions and geographies to advance development programs an...

Job DescriptionAssociate Principal Scientist Regulatory CMC - Biologics (R4)This Associate Principal Scientist position is equivalent to an Associate Director position.Under direction from Director/Executive Director the Assoc Principal Scientist is responsible for implementing Chemistry Manufacturi...

Job DescriptionDirector/Principal Scientist Devices and Drug-Device Combinations Regulatory CMCReporting to the Director of Device Regulatory Affairs for Autoinjector Development Programs the Director/Principal Scientist in Devices and Drug-Device Combinations CMC is responsible to support Device CM...

Job DescriptionDirector/Principal Scientist Devices and Drug-Device Combinations Regulatory CMCReporting to the Director of Device Regulatory Affairs for Autoinjector Development Programs the Director/Principal Scientist in Devices and Drug-Device Combinations CMC is responsible to support Device CM...

Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our Companys Oncology medicines span all phases of clinical development (pre-clinical to post-licensure...