GLOBAL CMC REGULATORY AFFAIRS jobs in United Kingdom

Manager - Remote - Contract Proclinical is seeking a Regulatory Affairs CMC Manager to support global commercial post... * Location: United Kingdom Leeds, England Posting date: 24 Apr 2024 Reference: RA.CS.60059b Regulatory Affairs CMC...

individual to take on the role of Regulatory Affairs CMC Manager to support global commercial post-approval submissions! Key...Position: Regulatory Affairs CMC Manager Location: Holborn, London Contract Length: Initial 12 Months - possibility...

Regulatory Affairs, CMC Product Teams and GRACS CMC teams. The primary activities may include but are not limited to the... following: Supports CMC regional regulatory strategies for new marketing applications, and post-approval changes Delivers...

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...

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

Job Purpose As a Senior Manager, Regulatory Affairs CMC, you are an integral part of MoonLake’s Clinical Development... Senior Manager, Regulatory Affairs CMC will serve as a subject matter expert, which will involve collaborating with multiple...

CMC leadership on the cross functional sub teams (Global Regulatory Affairs (GRA) Teams and Supply & Technology Solutions... in Regulatory Affairs CMC and/or in pharmaceutical manufacturing, analytical development, and quality assurance/control...

for a Regulatory Affairs CMC Manager with Post Approval Submissions and who has liaised with Global Regulatory bodies... of regulatory affairs CMC experience Site and global regulatory CMC experience Use of Software/tools such as Veeva vault...

as well as knowledge of global pharmaceutical legislation and guidance specifically linked to regulatory CMC aspects in the ICH countries...Regulatory Affairs Consultant. 8+ years' experience in handling life cycle management of approved drug products...

. This position would primarily support Amgen’s marketed products globally, as a Principal Regulatory Affairs CMC lead. The Manager..., submission strategy, and regulatory risk assessments Development of global dossiers for CMC content of new marking applications...

as required. Highlighted responsibilities: Products Responsible for appropriate Europe Region regulatory input to project teams and Global... Regulatory Slides via the Global Liaison and Global Regulatory Teams. Responsible for ensuring planned drug development...

as required. Highlighted responsibilities: Products Responsible for appropriate Europe Region regulatory input to project teams and Global... Regulatory Slides via the Global Liaison and Global Regulatory Teams. Responsible for ensuring planned drug development...

of ICH and other global regulatory guidelines; in-depth understanding of a regulatory speciality areas, such as preclinical, clinical, CMC... and/or global regulatory submissions and ensure high quality standards that meet or exceed client expectations, local and regional...

-product global regulatory CMC strategies for marketed products. This role contributes to the preparation and submission... regulatory CMC strategies for commercial products Works with regulatory colleagues in development of global regulatory CMC...