DIRECTOR REGULATORY CMC jobs in EVERETT MA, United Kingdom

Associate Director, Regulatory Affairs – CMC Who we are: is a biopharmaceutical company that is fueled... you will make: Agios Pharmaceuticals is searching for a dynamic Associate Director of Regulatory Affairs - CMC...

Director, Regulatory Affairs- CMC Who we are: is a biopharmaceutical company that is fueled by connections... you will make: Agios Pharmaceuticals is searching for a dynamic Director, Regulatory Affairs - CMC to join our growing Regulatory...

MOMA Therapeutics is looking for an experienced Director, CMC Lead Imagine joining a company... is seeking a Director of CMC Lead to join our growing development team as we drive two small molecule programs into clinical...

Senior Director/Vice President, CMC Company Overview Repertoire Immune Medicines is a biotechnology company working... and reports for inclusion in CMC sections of regulatory filings. Develop goals, operating plans, production milestones, and short...

from health authorities. This role reports into the Head of Pharma Process Development and Regulatory CMC. What You'll...Job Description About This Role The Sr. Director and Head, Analytical Development (AD)- Small Molecules & Antisense...

Job Description About This Role The strategic vision of Biogen's Global Reg CMC-Device, Packaging and Device... and maintain a strong network and partnership with R&D, Medical, Quality, Regulatory, Commercial, and across PO&T to ensure...

Be well versed in all stages of pharmaceutical development and understands the global regulatory trends for CMC activities, to ensure... CMC program leadership and oversight of Pharmaceutical Sciences (PS) with management and oversight of all project-related...

, Regulatory Affairs, CMC, QA, Pharmacovigilance, etc.) to achieve expected outcomes. Exhibited ability to problem-solve... reports to the Director of Clinical Operations and is an individual contributor to the successful achievement of the Clinical...

Reporting to the Director, Clinical Operations, the Senior Study Manager, Clinical Operations is responsible... a trial master file (TMF), so that documentation of GCP compliance is available, if required by a regulatory agency. Supports...