Compliance And Regulatory Jobs in Rahway, NJ

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 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 DescriptionThe Associate Director Quality Control within our Research and Development Division Device Quality & Regulatory is responsible for providing QA/QC oversight of the companys Device Network design verification laboratories. This role will provide quality oversight for the qualification...

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 DescriptionDigital Chemistry Manufacturing and Controls (dCMC) is a cross-divisional digital transformation initiative that will enable the pipeline by establishing a digital continuum of data from development through manufacturing for our products and processes.dCMC intends to deliver:Increased...

Job DescriptionAssociate Director Regulatory Submissions Archive OperationsLocation: Rahway NJ (Hybrid role - onsite 3 days per week required)Functional Area: Regulatory Innovation and Information Management (RIIM) within Global Regulatory Affairs & Clinical Safety (GRACS)The Associate Director of R...

Job DescriptionThe Associate Director Regulatory Affairs supports products in the Oncology therapeutic area as part of a regulatory team. The individual will have excellent communication and collaboration skills and will work closely with a global regulatory lead(s) to help develop and implement a g...