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Quality Engineer – Medical Devices
£21.62 - 12 month Contract
Cambridge
We are looking for an experienced Quality Engineer to join the team of an established Device Development Centre. The role will entail working on the full product life cycle, cross functional with the various teams and stake holders involved.
Expearience
• Relevant Degree or Higher Education Qualification
• History of working in accordance with the requirements of ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and the EU Medical Devices Regulation.
• Experience in design controls and risk management for combination products.
• Familiar with Human Factors Engineering - Usability Engineering.
• Familiar with device assembling manufacturing processes.
TECHNICAL SKILLS REQUIREMENTS.
• Working knowledge of ISO 9001, ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and the EU Medical Devices Regulation.
• Familiarity with EN 62366, EN 60601, and EN 62304.
• Able to learn and apply established procedures in a reliable and consistent manner.
• Capable of working independently with minimal supervision.
• High level of attention to technical details and accuracy.
• Able to prioritize multiple responsibilities and to work on multiple tasks simultaneously.
• Able to work collaboratively in cross functional teams.
• Excellent communication (e.g., oral, written, presentation) and interpersonal relationship skills.
• Proficiency in general computer software such as word processing, spreadsheets, presentations.
• Understand Good Manufacturing Practices (GMP).
