Regulatory Affairs Specialist

Roc Search; Maidenhead; On-site; GBP 50,000 - 65,000; Full time

Job summary

A leading surgical instrument manufacturer in Maidenhead is seeking a Regulatory Affairs Specialist to enhance their team. This immediate vacancy offers a chance to work in a fast-paced environment, focusing on compliance with medical device regulations and standards. Candidates should be prepared for an onsite role with future remote work potential, and the salary is competitive based on experience.

Skills

Medical Device Regulations (MDR)

ISO 13485

MDSAP

CE Marking

FDA

Audits

Class II Devices

Job description

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.