Regulatory Director Jobs
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Regulatory Affairs Director Ad/Promo
Director of Regulatory Affairs, Ad/PromoSalary: $188,000-$235,000 Summary:A leading biotech in Burlington, MA is seeking a dynamic and visionary Director of Regulatory Affairs for Advertising and Promotion. In this influential role, you'll partner with diverse cross‑functional teams to shape compelling, compliant promotional strategies that elevate...
Director, Regulatory Affairs CMC
OverviewAn established pharmaceutical organization is seeking a Director of Regulatory Affairs CMC Strategy to lead global regulatory planning and execution related to Chemistry, Manufacturing, and Controls (CMC). This role supports products from early development through post‑approval lifecycle management and serves as a key partner to CMC, Qualit...
Director Regulatory CMC
Director, Regulatory Affairs - CMC (Individual Contributor) Location: Flexible (U.S. based only, remote or hybrid options available) Employment Type: Full-timeSummary: A growing biopharmaceutical company is seeking a Director, Regulatory Affairs - CMC to lead global regulatory CMC activities to enable clinical development, commercialization and lif...
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Senior/Principal Scientist, LBA
Senior Scientist / Principal Investigator, Bioanalysis & Biomarkers(GLP/GCLP · LBA · PK/ADA/Biomarkers)Overview A leading CRO is seeking an experienced bioanalytical scientist to join its Bioanalysis & Biomarkers group. This team supports global pharmaceutical and biotech partners by delivering high‑quality GLP/GCLP bioanalysis, method development,...
Associate Director Regulatory Affairs
Associate Director / Director Regulatory AffairsConfidential Early‑Stage Biotech | San Diego, CA (Onsite Preferred / Hybrid Considered)Expected Compensation: $180-$200k base + bonus + equityWe're supporting a confidential, venture‑backed RNA therapeutics company in San Diego. They're backed by top-tier global biotech investors, and developing a pip...
Director, Regulatory Affairs
Overview We are seeking a seasoned Director of Regulatory Affairs to lead global regulatory strategy, submissions, and compliance activities supporting a dynamic portfolio of medical devices. The ideal candidate brings deep expertise in U.S. FDA pathways-particularly 510(k) premarket notifications-and hands-on oversight of labeling compliance throu...