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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 3 days ago by Science Solutions Recruitment
Hold a Scientific Degree. 1 years' experience within Pharmaceutical or Medical Device Regulatory Affairs. Expert organisation skills. Strong written and verbal communication skills. Benefits for the Regulatory Affairs Officer. Free on-site parking. No weekends. 25 Days holiday + bank … more
Posted 3 days ago by CK Group- Science, Clinical and Technical
CK Group are recruiting for a Business Insights, Analytics and Market Research Manager to join a global pharmaceutical company located in West London on a permanent basis with flexibility of hybrid working. Location. Our client is based in West London. This role offers hybrid working with … more
We found 4 jobs outside your search area.
Posted 2 days ago by Park Street People
Our client, a global pharmaceutical company, is currently looking for a CMC Regulatory Affairs Associate to join their team in Uxbridge. Working in a busy global department, there is a focus on working together to achieve results. You would be joining a company with an exciting pipeline who … more
Posted 3 days ago by CK Group- Science, Clinical and Technical
CK Group are recruiting for a Regulatory Partner Medical Devices to join a company in the Pharmaceutical industry at their site based in Welwyn Garden City on a permanent basis. Company. Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing … more
Posted 2 days ago by CK Group- Science, Clinical and Technical
CK Group are recruiting for a Regulatory Partner (Medical Devices) to join a company in the Pharmaceutical industry at their site based in Welwyn Garden City, on a contract basis for 12 months. Salary. Daily rate of either £367.54 - £452.36 PAYE or £487.50 to £600.00 Umbrella / Ltd company … more
Posted 3 days ago by Clearline Recruitment Ltd
Strong regulatory knowledge and experience in the medical devices (and preferably pharmaceutical) industry to support foundation and squad work within a regulated environment. Possess broad regulatory expertise to contribute to foundation and squad tasks, help develop squad/chapter plans … more
