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Displaying 1-6 of 6 jobs
The position you are looking for is no longer available, but here are some similar jobs that might interest you
Posted a week ago by Hyper Recruitment Solutions LTD
Key Words: Quality Control | QC | Microbiology | Microbiologist | Pharmaceutical | Biopharmaceutical | Quality Testing | GMP | GLP | Good Manufacturing Practice | Good Laboratory Practice | Quality | Documentation | Compliance | Regulated Environment | Environmental Monitoring | Aseptic … more
We found 5 jobs outside your search area.
Posted a week ago by G&J Lee Recruitment
Location: Hybrid working with regular time in a central London office. Package: Lucrative, uncapped bonus structure and a comprehensive, modern benefits package (details below. Responsibilities: Project Management and Client leadership for a diverse portfolio of Market Access, Value Communications, … more
Posted 6 days ago by Park Street People
Our client, a global pharmaceutical company, is currently looking for a CMC Regulatory Affairs Manager to join their team in Uxbridge on a temporary contract. This is a great opportunity to work for a pharmaceutical company who have created a centre of excellence and constantly … more
Posted 29/04/2024 by Park Street People
An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU and early stage development experience to join their team on a 12 month temporary contract. Working with the regulatory team (and core stakeholders across multiple areas), your … more
Posted 23/04/2024 by CY Partners
CY Partners have an exciting new opportunity as a Clinical Project Manager in a global pharmaceutical company, as part of their Health OC team. Are you looking for a high-profile Health OC role that shapes solid evidence generation for our medicines across the region? If so, this Clinical … more
Posted 30/04/2024 by CK Group- Science, Clinical and Technical
Educated to degree level or above in life sciences or a relevant field with significant experience in Regulatory Affairs in the pharmaceutical industry. Knowledge of regulatory procedures in region for MAAs, CTAs, post approval changes and amendments, extensions and renewals. Understanding … more
