05/04/2024 | Fulltime | | Germany | CV-Library | €69,059 - €77,691 / Year And follow-on care to implement lasting change within the medical device sector. Your responsibility as the Head of Quality & Regulatory Affairs will be to help take the product from Clinical to Commercial production on a global scale while working in a fast-paced, close-knit environment giving guidance
Save for later05/04/2024 | Fulltime | | Germany | CV-Library | €70,000 - €80,000 / Year With ISO related to med-tech such as 13485, ISO 14971 (or ISO 9001) and FDA - Experience with regulatory affairs for medical devices and QMS - Knowledge of, or experience with, in-vitro diagnostic medical devices regulation (MDD - MDR) IVDR and CFR - Exceptional communication skills, attention to detail
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