REGULATORY CMC DIRECTOR jobs in United Kingdom

Job title: Regulatory Affairs Director CMC - London A global Pharmaceutical company in Central London are seeking... a Regulatory Affairs Director CMC. The role will work across a portfolio of...

Description The Principal Scientist / Director responsibilities include but are not limited to: Serve as a Regulatory CMC Project... is responsible for developing and implementing Chemistry, Manufacturing, and Controls (CMC) regulatory strategies...

to address external questions regarding drug products. Position Summary The CMC Regulatory Director, Cell Therapy... lives. Read more: Description The GRS-CMC organization provides regulatory expertise related to CMC activities through...

best medicines for patients. The Role We're seeking an experienced Associate Director of Early Drug Substance/CMC to contribute.... As Associate Director Early Drug Substance/CMC, you will be responsible for developing and delivering innovative, breakthrough...

seeking an experienced Associate Director of Early Drug Substance/CMC to contribute to our mission to develop better medicines..., and a critical interface with our external vendors and Pharma collaborators. As Associate Director Early Drug Substance/CMC...

input from diverse disciplines (e.g., clinical, regulatory, market access, manufacturing, CMC, commercial, and other areas...: The GPAM Associate Director, Project Manager, is a core member of Early Drug Development and/or Late Drug Development...

seeking an experienced Associate Director of Biopharmaceutics to contribute to our mission to develop better medicines, faster.... In this role you will lead activities related to biopharmaceutics, develop-ability and early global CMC strategy to guide...

best medicines for patients. The Role We're seeking an experienced Associate Director of Biopharmaceutics to contribute...-ability and early global CMC strategy to guide the selection of clinical candidates, drug delivery, and clinical formulation strategies...

seeking an experienced Associate Director of Biopharmaceutics to contribute to our mission to develop better medicines, faster.... In this role you will lead activities related to biopharmaceutics, develop-ability and early global CMC strategy to guide...

that facilities/processes are compliant and support approval of new modality regulatory filings. our Technical CMC teams for end... implementation of required Quality Management System (QMS) elements, procedures, and systems to ensure quality and regulatory...

e.g. CMC, Clinical Development, Regulatory, Research · Understanding of the requirements of key regulatory deliverables...Role Level: Manager Location: London Reporting to: Director – Program & Portfolio Management Job summary The...