Regulatory Affairs Jobs in Rahway, NJ

Job DescriptionThe Distinguished Scientist/Executive Director within Companion Diagnostics (CDx) Development will lead one of our companys Diagnostic Development Teams (DxDTs) supervising PhD-/MD-level employees developing and overseeing CDx strategy development alignment and execution for specific...

Job DescriptionOur Animal Health Marketing team takes a customer centric perspective using customer feedback and market intelligence data. Using this data we design develop and deploy products platforms brands and marketing initiatives that ensure we can improve the health and well-being of animals...

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 DescriptionGRACS CMC Principal Scientist CMC Pharm Pre-approval (Inhalation/Respiratory Franchise)Reporting to the Ex-Director/ Sr. Director in Pre-approval Pharmaceutical CMC is responsible for developing and implementing CMC regulatory strategies for our Companys pharmaceutical pipeline prod...

Job DescriptionGRACS (Global Regulatory Affairs & Clinical Safety) CMC Associate Principal Scientist CMC Pharm Pre-approval (Respiratory/Inhalation Products)This Associate Principal Scientist in Pre-approval Pharmaceutical CMC will be responsible for developing and implementing CMC regulatory stra...

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. Our companys Oncology medicines span all phases of clinical development (p...

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 DescriptionRole SummaryThe Associate Director Scientific Patient Engagement and Advocacy Lead General/Specialty Medicine is responsible for developing and implementing a global headquarters strategic patient engagement plan aligned with therapeutic objectives ensuring the patients perspectives r...

Job DescriptionRole SummaryThe Associate Director Scientific Patient Engagement and Advocacy Lead General/Specialty Medicine is responsible for developing and implementing a global headquarters strategic patient engagement plan aligned with therapeutic objectives ensuring the patients perspectives 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 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 DescriptionThe Senior Clinical Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the insert name of TA therapeutic area. Our companys insert name of TA medicines span all phases of clini...

Job DescriptionOur Clinical Development teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs and new indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and app...

Job DescriptionOur Clinical Development teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs and new indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and app...

Job DescriptionThe 2-year Physician Scientist Program provides pharmaceutical medicine training and opportunities to physicians completing residency or fellowship with the goal of recruiting new talent and contributing to the organizations inclusion objectives. The program provides in-depth exposure...

Job DescriptionOur company in the United States and Canada 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...

Job DescriptionThe Future Talent Program features Cooperative (Co-op) education that lasts up to 6 months and will include one or more opportunities in our Research and Development Division can provide you with great development and a chance to see if we are the right company for your long-term goa...

Job DescriptionThe Business and Information Architecture (BIA) group within our Research & Development Division Clinical Development and Digital Solutions (CDDS) value team the Business Strategy Partnership (BSP) organization is seeking a highly motivated Senior Specialist / Information Architect. T...

Job DescriptionJob SummaryWe are seeking a highly experienced and motivated individual to join our team as the Director of Biologics- Materials and Biophysical Characterization. The successful candidate will lead our biophysical characterization group in biologics overseeing the analysis and interpr...

Job DescriptionWere seeking a Growth- and Improvement-minded leader to build a purpose-built customer experiencedriven omnichannel engine across our U.S. Animal Health portfolio. You will lead a team that owns digital demand creation and customer experience for veterinarians producers distributors a...