Regulatory Affairs MDR Engineer

London Permanent View Job Description
Fantastic opportunity to join a dynamic team launching innovative technology within the medical technology sector.
  • Fantastic opportunity to join an innovative medical devices manufacturer
  • Great opportunity to be apart of a dynamic team working on exciting projects

About Our Client

My client is an innovative medical devices manufacturer based in London, England.

Job Description

Quality Management - following process and procedures in compliance with ISO13485/MDR QMS system

Design support - team member with contributory role to new product design

The Successful Applicant

Good understanding of reporting requirements under MDR/ISO-13485

Flexibility and Resilience

Quality objectives- The desire to meet the needs and expectations of regulatory compliance and product quality

What's on Offer

Competitive package available

Contact
Kelly Percival
Quote job ref
JN-012025-6627985
Phone number
+44 1727 730 143

Job summary

Job function
Life Sciences
Subsector
Regulatory Affairs
Sector
Healthcare / Pharmaceutical
Location
London
Contract type
Permanent
Consultant name
Kelly Percival
Consultant phone
+44 1727 730 143
Job reference
JN-012025-6627985