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Day to day tasks: - Develop test strategies for the projects - Support project teams in carrying out the detailed test plan and evaluation of test results - Ensure and maintain product quality leading to market release - Support the project team during risk assessment of products and production processes - Ensure the successful implementation of all quality-related aspects of the product and project documentation - Participate in continuous process improvement and documentation within R&D - Ensure verification and validation tasks are performed and documented in compliance with ISO 13485/QSR-requirements - Help coordinate R & D staffing to ensure the above tasks are performed as necessary Your profile: - A basic technical training (FH / ETH) with training in quality techniques : 3 - 5 years experience in the manufacture and development of equipment or machinery, preferably in the medical, pharmaceutical, aerospace, or automotive industry - Good knowledge of the ISO 13485 and QSR requirements are an advantage - Fluent English is required as is German. Excellent communication and interpersonal skills are essential. For more information on this vacancy, or any other medical device opportunities, please contact the Senior Consultant Andrew Boroky on 0044 (0) 207 940 2116, or email him at a.boroky@nonstop-devices.com