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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 2 weeks ago by Hyper Recruitment Solutions LTD
Based in Berkshire, this role offers the chance to become an integral part of a leading Pharmaceutical company, ensuring that innovative health solutions reach the market efficiently and safely. As a Regulatory Affairs Executive, your role will be instrumental in supporting the … more
Posted 11/04/2024 by Hunter AHP Resourcing
The post holder will help assist the Production Manager in overseeing the licensed Pharmacy Production Unit as well as the trust's Cytotoxic Dispensing Unit in accordance to a professional pharmaceutical service laid out by NHS England. Working hours are 8:30am - 4:30pm w/ a 30 minute break … more
We found 4 jobs outside your search area.
Posted 09/04/2024 by Michael Page
This role requires a Supply Planning Excellence Lead who can effectively manage and enhance the supply chain processes within the life science industry. The candidate should exhibit strong leadership skills and have a comprehensive understanding of Supply Planning processes. Client Details. The … more
Posted 4 days ago 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 2 days ago by PE Global International
PE Global is recruiting a Regulatory Affairs Manager (CTA) for our multinational pharmaceutical client based in Uxbridge. The role is hybrid and an initial 12-month contract. Responsibilities of the role. Advising the GRT on regional considerations in developing strategy. Ensuring the … more
Posted 3 days ago 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
