- J&J Family of Companies (Boston, MA)
- Associate Director , CMC Regulatory Affairs - 2406221330W **Description** Johnson & Johnson is recruiting for an Associate Director , CMC ... of development and commercialization. This person is responsible for developing global CMC regulatory strategies. The primary responsibility is to work on… more
- Takeda Pharmaceuticals (Boston, MA)
- …my knowledge. **Job Description** Takeda Development Center Americas, Inc. is seeking an Associate Director , CMC Program Lead, Cell Therapies in Cambridge, ... and product quality improvement in Chemistry, Manufacturing & Control ( CMC ) processes; Employ technical project management principles (project planning, RACI,… more
- WuXi AppTec (Boston, MA)
- …needs in TIDES drug development from discovery through clinical to commercial. Moreover, our Regulatory Affairs CMC team is experienced in preparing CMC ... drug). We greatly simplify the TIDES drug development by providing all discovery, CMC development and the entire manufacturing supply chain under one roof. With over… more
- Sanofi Group (Framingham, MA)
- **Job Title:** Associate Director , Upstream MSAT **Location:** Framingham, MA **About the Job** We are an innovative global healthcare company with one purpose: ... you thought was possible. Ready to get started? The Associate Director position is part of the...responsible for preparing reports and other internal documentation for regulatory purposes. + Collaborate with MSAT and CMC… more
- Regeneron Pharmaceuticals (Cambridge, MA)
- We are seeking an enthusiastic ** Associate Director , Program & Portfolio Management** to drive programs forward at Regeneron Cell Medicines (RCM) through ... on programs that are in IND-enabling studies through clinical study execution. **As an Associate Director , Program & Portfolio Management at RCM, a typical day… more
- AbbVie (Cambridge, MA)
- …functional groups to provide a unified clinical pharmacology position to clinical, CMC and regulatory teams. Authors scientific publications and present at ... Pharmacology development plans and strategies that achieve commercial goals and regulatory requirements for multiple functions. + Generates new PK/PD study proposals… more
- Takeda Pharmaceuticals (Boston, MA)
- …experience within related functions (eg Clinical Science, Clinical Operations, Research, Regulatory , CMC , Marketing) + 3-5 years program management experience ... leading complex pharmaceutical projects in a multi-disciplinary, global environment + Demonstrated ability to positively influence outcomes, key project decisions, and strategic problem-solving + Proven ability to communicate clearly and present key… more