Job Description
Sinclair is Hiring! Join Our Team as a Regulatory Affairs Specialist 🚀
We are currently recruiting for Regulatory Affairs Specialist in the UK. The Regulatory Affairs Specialist will be responsible for regulatory activities in support of lifecycle management for injectable medical device products at Sinclair. This Regulatory Affairs Specialist will support a variety of responsibilities and requirements within the company to achieve agreed targets and schedules to maintain/obtain new and current authorisations/registrations for injectable medical device products. The RA Specialist supports regional markets (EU/CEE) and is part of the RA team.
The ideal candidate will have 3-5 years experience in Regulatory Affairs
Location: 3 days a week in either our Chester or London office
About Sinclair
Founded in 1971, Sinclair is a global medical aesthetics organisation, that delivers an extensive product range. With an in-house commercial infrastructure, including manufacturing and a network of distributors in leading global markets, our products are sold in 55 countries worldwide.
This is a great time to join Sinclair as we continue to increase our product range and expand into new markets and territories.
Sinclair Values:
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