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 : 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. ADZN1_UKTJ