- Abbott (St. Paul, MN)
- …life Sciences, Biology (or equivalent vocational qualifications) + Experienced in regulatory submissions for Pharmaceutical , In vitro diagnostic devices and/or ... female executives, and scientists **The Opportunity** We are seeking a **Principal Regulatory Affairs Specialist** to join Abbott's Vascular Division on-site in St.… more
- Takeda Pharmaceuticals (Boston, MA)
- …bring life-changing therapies to patients worldwide. The Associate Director, Global Regulatory Affairs Advertising and Promotion (GRA A&P) Review Lead is accountable ... medicine promotion. **How you will contribute:** + As our Associate Director, Global Regulatory Affairs Advertising and Promotion lead you will act as the Subject… more
- Abbott (Plymouth, MN)
- …scientific affairs function. **Preferred** **Qualifications** + 4+ years of related regulatory submission experience from medical device, pharmaceutical , or ... their lives. **The Opportunity** Abbott is seeking a passionate, experienced **Senior Regulatory Affairs Specialist** to join our team on-site in Plymouth, MN. In… more
- BeOne Medicines (San Mateo, CA)
- …and other business functions in the United States and Canada to ensure compliance with applicable regulatory requirements and guidelines, and consistency with ... **General Description:** The Manager, Regulatory Advertising and Promotion will be responsible for...discipline, 5 years of experience in the biotechnical or pharmaceutical industry, and a minimum of 2 years' experience… more
- University of Pennsylvania (Philadelphia, PA)
- …He/she will, with minimal supervision, prepare and process all required regulatory documentation for pharmaceutical companies, contract research organizations ... in study team meetings, research team meetings, and ongoing protocol training/ compliance meetings. The Regulatory Affairs Specialist-CC is expected to… more
- Rhythm Pharmaceuticals (Boston, MA)
- …of operations resources for submission documents + Identify new or revised regulatory policies and initiate activities to support compliance + Participate ... life/physical sciences or related field + 8+ years of highly relevant pharmaceutical /biotechnology experience in Regulatory Affairs Operations + Knowledge and… more
- Sanofi Group (Morristown, NJ)
- …Safety, and Medical Affairs, to ensure labeling content reflects scientific integrity, regulatory compliance , and supports safe and effective product use. We ... to maximize labeling value. + Assist in labeling submissions, regulatory queries, and updates to ensure compliance ...or medically related field. + Minimum 5+ years of pharmaceutical industry experience, with at least 3 years in… more
- Rhythm Pharmaceuticals (Boston, MA)
- …team, you'll be responsible for the effective management and timely execution of regulatory filings, maintaining compliance with global regulatory standards ... timelines + Ensure effective and timely execution of regulatory filings in compliance with relevant ...in drug development and product registration activities within the pharmaceutical or biotech industry in multiple phases of development… more
- Lilly (Philadelphia, PA)
- …through philanthropy and volunteerism. **Position Overview:** The Manager, Manager- CMC Regulatory is responsible for the preparation and delivery of high-quality ... CMC regulatory submissions. This position supports Lilly/Avid diagnostic radiopharmaceutical marketed...chemistry or related field, or PharmD + Experience in pharmaceutical development and/or manufacturing with a minimum of two… more
- Sanofi Group (Morristown, NJ)
- …project timelines for clinical trial initiation. + Supports operational and compliance activities for assigned deliverables, develops, executes regulatory ... **Job Title:** Regulatory Strategist **Location:** Morristown, NJ/Cambridge, MA **About the...field) preferred. + At least 6 years of relevant pharmaceutical /biotechnology experience, including at least 4 years of relevant… more