Regulatory Affairs Manager

Regulatory Affairs Manager
  • £35,000 - £45,000 per Annum
    ANNUM
  • Permanent
  • Leeds, West Yorkshire, England, UK LS14 6UF Leeds West Yorkshire UK LS14 6UF
Job Ref: J2157654
Sector: Engineering
Sub-sector: Medical Devices
Date Added: 06 November 2020
Regulatory Affairs Senior Specialist/Manager role for a small but well-established Medical Device company in Leeds

Regulatory Affairs Senior Specialist - Medical Devices - Leeds

Are you a QA/RA professional looking for that next step? Does working for a small innovative company excite you more than a global giant? If so, give me a call ASAP.

A small but well-established Medical Device company is looking for a Regulatory Affairs Specialist/Manager to join their QA/RA department reporting into the Managing Director. It is a vital role for the company as you ensure the company is adhering to all relevant regulations. This will involve developing compliance strategies, completing and submitting documentation, working with international distributers and being the subject matter expert on MDR and UKCA regulations for Class III products.

Ideal experience and skills:

* A Bachelor's degree or higher in a life science discipline

* 3+ years' experience within Medical Device Quality Assurance

* Strong understanding and experience of MDR and Class III products

* Experience with clinical evaluation reports (CER) and post-market surveillance (PMS)

* Strong leadership skills and ability to own the MDR regulation compliance

* Networking ability, both internally and externally

To find out more information please contact Alex Eager on the following details.Alex.Eager@srgtalent.com0161 868 2226

SRGTalent
06/12/2020 09:57:50
GBP 35000.00 35000.00
Contact Consultant:
Laith Mustafa

Submitting application, please wait..