Latest Drug Regulatory Affairs jobs in South San Francisco, CA

10 Drug Regulatory Affairs Jobs in South San Francisco, CA

Associate Director, Clinical Science Maze Therapeutics - South San Francisco, CA, United States and budgets for clinical activities with overall company timelines and goals, in close coordination with project management, CMC, nonclinical development, regulatory affairs, and other stakeholders. Skills 12 days ago
Associate Director, Formulation and Drug Delivery Astrix - South San Francisco, CA, United States , Regulatory Affairs, and Manufacturing. Leading the developability assessment of new candidates, preclinical formulation, preformulation, and discovery pharmaceutics studies including API form selection 25 days ago
Regulatory Affairs Manager AbbVie - South San Francisco, California communication on Regulatory/FDA issues including Public Affairs, Clinical Development, Legal, & others such as Commercial. Interpret FDA/European Medicines Agency (EMA) regulations, guidelines, policy statements 8 days ago
Senior Director Regulatory Affairs Meet - Redwood City, CA, United States Senior Director, Regulatory Affairs (Generalist) Hybrid Role - 3 Days in Menlo Park, CA Meet is partnering with a late stage pediatric rare disease startup looking for a high-level Regulatory Affairs 12 days ago
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Senior Director Regulatory Affairs Meet - Redwood City, CA, United States the development of innovative drug products. This role requires a strong understanding of global regulations and extensive experience in regulatory affairs within the biotechnology or pharmaceutical industries 22 days ago
Senior International Regulatory Product Specialist – Diabetes Care (on-site) Abbott Laboratories - Alameda, California , engineering, or medical fields. Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society.) 2-3 years of experience in regulatory preferred but may consider quality assurance 7 days ago
Director, CMC Regulatory Affairs Bayside Solutions - Fremont, CA, United States related field is preferred. 15+ years of pharmaceutical/biotech drug development experience with 5+ years of experience in global CMC regulatory affairs with working experience and content knowledge in CMC 17 days ago
Director Toxicology (Remote) Jazz Pharmaceuticals - Palo Alto, California subject matter expertise to key internal functions (regulatory, Quality, Clinical, CMC and formulations, Product Quality, Drug safety, Medical affairs) and their external contractors or collaborators 21 days ago
Director, Regulatory Affairs, Oncology - Job ID: 1311 Ascendis Pharma - Palo Alto, California with drug-device combination products preferred, but not required · Experience in filing regulatory dossiers including CTAs, IMPDs, INDs required; experience with BLAs/NDAs/MAAs is a plus · Ability to travel 23 days ago
Manager, Regulatory Affairs: Job ID- 1322 Ascendis Pharma - Palo Alto, California viewpoints and perspectives to all aspects of the business, from drug development to marketing. The Manager, Regulatory Affairs will be responsible for supporting and developing global regulatory strategies 25 days ago

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