- BeOne Medicines (San Mateo, CA)
- …assigned projects. The individual will provide support to cross-functional teams on CMC regulatory strategies and process optimizations on relevant topics. ... **Essential Functions of the job:** + Lead, develop and implement small molecule CMC regulatory strategies as well as authoring CTD CMC sections for the… more
- Kelly Services (South San Francisco, CA)
- …rate:** $60-80/hour Be at the forefront of innovative small molecule drug development as the Associate Director of Project Management, CMC . You will play a ... innovation and operational excellence. You'll work closely with cross-functional leaders across CMC , Drug Development, QA, Regulatory , and external partners to… more
- Sumitomo Pharma (Sacramento, CA)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Director , Regulatory Affairs (Oncology).** The Associate ... Director is part of the Global Regulatory Affairs (GRA) team based in the US. He/She...the global regulatory lead (GRL) and the CMC regulatory lead in the formulation of… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- ** Associate Director , Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and ... drug substance and drug product ensuring compliance with relevant ICH and regulatory guidelines + Develop and implement stability study protocols and timelines,… more
- Takeda Pharmaceuticals (Thousand Oaks, CA)
- …true to the best of my knowledge. **Job Description** **About the role** As Associate Director , API Process Engineering, you will be Takeda's global expert for ... strategy), site leadership, Technical Services, Pharmaceutical Sciences, Global Quality, and Regulatory CMC . + Provide technical support to marketing… more
- Takeda Pharmaceuticals (Thousand Oaks, CA)
- …true to the best of my knowledge. **Job Description** **About the role** As Associate Director , Drug Product Manufacturing Science & Technology, you will be ... effectively with local Technical Services, site leadership, Pharmaceutical Sciences, Global Quality, Regulatory CMC , and other key functions to align on… more
- University of Southern California (Los Angeles, CA)
- …cell and gene therapies and other biological products for internal/external users. The Associate Director of Process Development (cGMP) is responsible for all ... interactions and activity prioritization. Regularly ensures compliance with all relevant regulatory requirements. + Oversees the implementation of project plans (eg,… more
- Kelly Services (South San Francisco, CA)
- Kelly(R) Science & Clinical is seeking an Associate Director / Director of Drug Substance Manufacturing for a direct hire opportunity with a leading ... Senior Director , $275,000 - $320,000 **Overview** As Associate Director / Director , Drug...our investigational and commercial portfolio. Reporting to the Senior Director of CMC , you'll be instrumental in… more
- LA Care Health Plan (Los Angeles, CA)
- …maintain a high level of based knowledge on benefits for all product lines (Medi-Cal, CMC , PASC, Healthy Kids and Covered California) as well as serve and act as the ... and support trainers with academy classes. Duties Conduct audits to ensure that regulatory and quality requirements were met across all verticals under CSC. Conducts… more