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A quality manager is being sought to take responsibility for ensuring that the Company's product development and manufacture adheres to the requirements of EU and US regulatory authorities and facilitate the progression through to clinical trial to enable the company to achieve its commercial objectives.
The successful candidate will have a proven track record in quality management. They will have experience of setting up and managing an ISO 9000 based quality management system, preferably ISO13485. Knowledge and experience of the medical device directive and regulatory aspects of Class IIb or III implantable medical device development projects from early stage to successful clinical trial is preferred.
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