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Quality and Regulatory Manager (Medical Devices)

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Posted By: Volt Europe
Address:
Date Posted: 9th Feb 2010
Salary: GBP per annum + Benefits
Location: Bedford
Reference Code: 2185778
Views Since Posting: 178
Full Description:

Join a innovative and outcomes focused healthcare company that provide tailored medical device solutions.

As a Quality and Regulatory Manager you will ensure that operations and products are in compliance with applicable regulatory requirements, manage the QRM department day-to-day activities and develop quality awareness in the medical device design and development division. You will have budgetary responsibility for the division and lead a team of up to 6 people.

To be successful in this position you will most likely have a degree or higher in an appropriate Science/Technical discipline, together with significant experience in senior quality or technical management roles, with at least 3 years in a senior quality management position with line management responsibility. A comprehensive knowledge of ISO9001, ISO13485, Medical Device Directive and FDA QSR820. You will also ideally have knowledge or experience of product development processes relating to electro-mechanical medical devices

Volt Europe is an established global recruitment business with an international presence spanning the IT, digital entertainment, finance and pharmaceutical sectors.

Volt Life Sciences recruits within biostatistics, clinical research, regulatory affairs, medical affairs, quality assurance, pharmacovigilance and medical sales & marketing. We recruit for both permanent and contract positions on a Pan-European basis.

Volt Europe's Quality Management System complies with ISO9001: 2008 and has been certificated since 1993. Our processes mirror those developed by our parent company, which is a Six Sigma organisation. Volt Europe is a member of APSCo, the Association of Professional Staffing Companies.

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