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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:
- 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.
