- Gilead Sciences, Inc. (Foster City, CA)
- …liver diseases, cancer and inflammation, and serious respiratory and cardiovascular conditions. ** Director , CMC Regulatory Affairs - Biologics** ... **Key Responsibilities:** The Director , CMC Regulatory Affairs for Biologics is responsible for defining regulatory strategy for one or more… more
- Gilead Sciences, Inc. (Foster City, CA)
- …and help create possible, together. **Job Description** **Associate Director , Analytical Regulatory Sciences, Systems & Operations in CMC Reg Affairs :** ... be accountable for the interpretation and implementation of new and existing CMC regulatory guidelines and regulations to ensure approvability globally. **Job… more
- Ascendis Pharma (Palo Alto, CA)
- …a dynamic workplace for employees to grow and develop their skills. The Associate Director , Regulatory Affairs will be responsible for developing and ... implementing global regulatory strategies encompassing clinical, non-clinical and CMC ...complex and require extensive interaction with departments outside of regulatory affairs . + Excellent organizational skills and… more
- Gilead Sciences, Inc. (Foster City, CA)
- …regulations to ensure approvability globally. The incumbent will report directly to Head of CMC Regulatory Affairs - Systems and Operations at Gilead. ... 35 countries worldwide, with headquarters in Foster City, California._ **Senior Director - Analytical Regulatory ** **Science** **KEY** **RESPONSIBILITIES** The… more
- Gilead Sciences, Inc. (Foster City, CA)
- …with Small Molecule Drug Substance Development, Small Molecule Drug Product Development, CMC Regulatory Affairs , Quality Control and Manufacturing Operations ... Join Gilead and help create possible, together. **Job Description** ** Director , Small Molecule Analytical Development, Analytical Development and Operations (ADO)**… more
- US Tech Solutions (South San Francisco, CA)
- + We are currently seeking a Regulatory Affairs Associate Director / Director to join our growing regulatory team. + In this role you would be the ... strategies for oncology products including clinical, nonclinical and CMC aspects and identify potential risks associated with proposed...- 9 ( director ) years of experience in Regulatory Affairs (strong preference for experience in… more