Quality And Regulatory Consultant - Medical Devices - Contract

Medical Device Quality and Regulatory Consultant - Contract Opportunity

Location: Greater Manchester (Hybrid)

Contract: 6 months initially

Rate: Up to £500 per day (Outside IR35)

Start Date: ASAP

KO2's exclusive client is developing a life-changing Medical Device and is seeking an experienced QA/RA Consultant to support their Quality Assurance & Regulatory Affairs efforts.

The Role:

1. Lead QA/RA activities, ensuring compliance with Medical Device regulations
2. Take ownership of QMS implementation and Technical Files
3. Focus on FDA 510(k), ISO 13485, and IEC 62304 compliance
4. Work on a multi-disciplinary Medical Device project (Electronics, Software, Mechanical, Clinical)
5. Join a dynamic start-up where you can make a real impact on Quality Assurance & Regulatory Affairs

This is a hands-on role in a growing business with a fantastic culture - where collaboration, respect, and motivation drive innovation.

A one stage interview can be quickly arranged.