- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- **Job Description Summary** As Associate Director, Regulatory Affairs, you will be responsible for leading RA team members involved in device project activities ... within the pharmaceutical or medical device industries, ideally with expertise in drug -device combination products; experience in regulatory and/or R&D, quality… more
- Rhythm Pharmaceuticals (Boston, MA)
- …learn, and our tenacity to overcome barriers, together. Opportunity Overview In the Associate Director, Regulatory Affairs role, you will be responsible for ... degree in life sciences preferred + 8+ years of Regulatory Affairs experience in drug development and...8+ years of Regulatory Affairs experience in drug development and product registration activities within the pharmaceutical… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Associate Director, Global Regulatory Affairs Advertising and Promotion **Location** : Cambridge, MA Morristown, NJ **About the Job** Are you ... of medicine? The race is on to speed up drug discovery and development to find answers for patients...accelerate progress. This individual will be responsible for providing regulatory review and approval of US promotional and other… more
- Gilead Sciences, Inc. (Foster City, CA)
- …BA/BS with 10+ years' relevant experience. + 4+ years' experience in prescription drug labeling. + Significant regulatory experience in the biopharma industry is ... their aspirations. Join Gilead and help create possible, together. **Job Description** Regulatory Affairs Labeling is a core function within Gilead's Global … more
- Bausch Health (Bridgewater, NJ)
- …itwhere your skills and values drive our collective progress and impact. The Associate Director, Regulatory Affairs handles regulatory development and ... Participates on the product development/life-cycle management team to provide regulatory guidance for assigned pharmaceutical products. Primary focus on approved… more
- Takeda Pharmaceuticals (Boston, MA)
- …experience + Preferred experience in reviewing, authoring, or managing components of regulatory submissions. + Solid working knowledge of drug development ... + Defines, develops and leads global strategies to maximize global regulatory success towards achievement of program objectives for complex and/or multiple… more
- AbbVie (North Chicago, IL)
- …drug development, including on clinical trial design and study requirements, regulatory exclusivities, orphan drug designations, and combination products, and ... YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description As an Associate General Counsel in the R&D Innovation Legal group, you will support… more
- Chiesi (Cary, NC)
- …and rewarding work. Who we are looking for Purpose Responsible for the regulatory review and submission of advertising and promotional materials for all Chiesi ... and changes to existing labeling, and submission of labeling information to regulatory authorities in the United States and Canada. Main Responsibilities +… more
- Organon & Co. (Jersey City, NJ)
- …project teams and alliance partners to develop and implement world-wide regulatory strategies for assigned biosimilar projects, with a specific focus on ... Regulatory CMC (Chemistry, Manufacturing, and Controls) requirements. This role...and medical leave, and health benefits including medical, prescription drug , dental, and vision coverage in accordance with the… more
- Amneal Pharmaceuticals (Piscataway, NJ)
- … regulatory processes. Additional Responsibilities: + Maintain awareness of all regulatory activities regarding new and approved drug products. Stay current ... and company goals and objectives. Essential Functions: + Develop and Execute Global Regulatory Strategies: Formulate and lead global CMC and clinical regulatory … more