GLOBAL CMC REGULATORY AFFAIRS jobs in UNITED KINGDOM, 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...

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...

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...

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...

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...

. 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...

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...

with regulatory registration strategy. Support the build of global clinical development strategy based on correct interpretation... from within a consultancy firms, healthcare authority (MHRA, EMA or any other EU Authority) with focus on regulatory affairs and clinical...

collaboration with multiple functions (External Sourcing and Manufacturing, Quality Assurance, Quality Control, Regulatory Affairs... entire network of Eurofins companies. Eurofins PSS Insourcing Solutions® is a global, award-winning insourcing solution...

collaboration with multiple functions (External Sourcing and Manufacturing, Quality Assurance, Quality Control, Regulatory Affairs... entire network of Eurofins companies. Eurofins PSS Insourcing Solutions® is a global, award-winning insourcing solution...