Medical Device Quality and Regulatory Consultant - Contract OpportunityLocation: Greater Manchester (Hybrid)Contract: 6 months initiallyRate: 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 and Regulatory Affairs efforts. The Role:Lead QA/RA activities, ensuring compliance with Medical Device regulationsTake ownership of QMS implementation and Technical FilesFocus on FDA 510(k), ISO 13485, and IEC 62304 complianceWork 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 and 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.