Good Afternoon,
My client, a surgical instrument manufacturer based in Maidenhead, is seeking a Regulatory Affairs Specialist to join their growing business.
This is an immediate vacancy, and I am eager to hear from candidates interested in joining a fast-paced company with a forward-thinking workforce.
Desired Experience:
1. Medical Device Regulations (MDR)
2. ISO 13485
3. MDSAP
4. CE Marking
5. FDA
6. Audits
7. Class II Devices
This role is primarily onsite, with some potential for remote work in the future. Please consider this before applying. This is an excellent opportunity to join a Life Science business manufacturing life-changing and life-saving equipment for the global market. Salary is dependent on experience, up to £65k.
To discuss this opportunity in detail, please send an up-to-date CV in response, and I will contact you at the earliest convenience.
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