- University of Southern California (Los Angeles, CA)
- …gene therapies and other biological products for internal/external users. The Associate Director of Process Development ( cGMP ) is responsible for all ... aspects of operations related to the current Good Manufacturing Practices ( cGMP ) laboratory, including manufacturing and process development activities, in order… more
- Takeda Pharmaceuticals (Thousand Oaks, CA)
- …is true to the best of my knowledge. **Job Description** **About the role** As Associate Director , API Process Engineering, you will be Takeda's global ... the "Apply" button, I understand that my employment application process with Takeda will commence and that the information...+ At least 5 years of experience in a cGMP manufacturing environment and at least 5 years of… more
- Charles River Laboratories (Northridge, CA)
- …at HemaCare, you will make a difference every day. **Job Summary** The Associate Director , Technical Excellence is responsible for oversight of Technical ... current Good Laboratory Practice (cGLP) and current Good Manufacturing Practice ( cGMP ) compliant Cell & Gene Therapy (C>) products.. Essential Responsibilities +… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …implement the strategy for Document Control to drive sustained compliance of CGMP /GDP activities. + Develop and implement a comprehensive global document control ... trends and best practices in document control. + Identify opportunities for process improvement and innovation. + Implement changes to enhance the efficiency and… more