- BeOne Medicines (San Mateo, CA)
- …and process optimizations on relevant topics. **Essential Functions of the job:** + Lead , develop and implement small molecule CMC regulatory strategies as well ... CMC regulatory strategies for the assigned projects. + Lead regulatory risk assessment, identify key CMC ...+ Lead regulatory risk assessment, identify key CMC regulatory issues and mitigation activities needed throughout product… more
- Sumitomo Pharma (Sacramento, CA)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Director , Regulatory Affairs (Oncology).** The Associate ... registration strategy of the product + Supports the global regulatory lead (GRL) and the CMC regulatory lead in the formulation of regulatory strategy,… 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 ... Takeda's manufacturing network and external CMOs. **How you will contribute** + Lead the Small Molecules API Manufacturing Sciences activities within Global Process… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Process & Operational Excellence (OpEx), and part of the larger PDM organization, the Associate Director , Business Processes & OpEx will support the success of ... than 35 countries worldwide, with headquarters in Foster City, California. ** Associate ** ** Director , PDM Business** **Process &** **Operational Excellence**… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Join Gilead and help create possible, together. **Job Description** The Associate Director , Strategic Sourcing & Supplier Management, Medical Devices ... operations team members for recurrent or chronic performance issues with supplier. + Lead annual business review meetings (BRMs) with assigned suppliers as needed + … 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 ... subject matter expert for small-molecule drug product and packaging. You will lead how tablets, capsules, and injectable products are industrialized, transferred to… 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 ... in professional organizations, meetings, conferences, seminars, and training courses. + Lead process development and optimization efforts of cell therapy products,… more