Contract Quality Assurance (QA) / Regulatory Affairs (RA) Consultant - Medical Devices

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:

• Lead QA/RA activities, ensuring compliance with Medical Device regulations
• Take ownership of QMS implementation and Technical Files
• Focus on FDA 510(k), ISO 13485, and IEC 62304 compliance
• Work on a multi-disciplinary Medical Device project (Electronics, Software, Mechanical, Clinical)
• 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.