About the Role:
I am partnering a well established Medical Device company based in Cheshire who manufacture and distribute a range of products are looking for a Quality Assurance & Regulatory Affairs specialist on a part-time basis - ideally 3 days a week on site in Macclesfield.
It is a permanent but part-time position so Consultants need not apply!
The company are offering up to £45k basic salary (full time equivalent) + package.
The Quality Assurance & Regulatory Affairs Specialist will be responsible for maintenance and updating of their QMS to ISO [... Click Apply...]6 and maintaining Technical files for the EMEA market initially but with plans to expand into other regions including the USA.
You must have knowledge and at least 3 years of working experience with ISO 13485 and MDD but also with an understanding of the new MDR changes and previous experience liaising with Notified Bodies.
Sthree UK is acting as an Employment Agency in relation to this vacancy.