A medical device firm is seeking an experienced Quality Engineer for a 6-9 month onsite contract in York, UK. The role requires leading validation programs, managing quality compliance issues, and driving risk management activities. Candidates must have extensive experience in the medical device industry and knowledge of ISO 13485. The position offers an opportunity for impactful contributions within a regulated landscape, focusing on enhancing quality and efficiency. Immediate availability is necessary, with the role being site-based five days a week.
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