06.06.24 | Teilzeit | Heidenheim an der Brenz | Paul Hartmann AGAnd/or experience in the areas of medical devices, technical documentation and regulatory product documentation, conformity assessment and post-market surveillance - Ideally a strong interest in and knowledge of electronic regulatory document control and management systems and associated processes - Open
Später ansehen03.05.24 | Vollzeit | Heidenheim an der Brenz | PAUL HARTMANN AG• Technical responsibility for a dedicated product assortment in the field of negative pressure wound care • Collaboration with other departments e. g. marketing, production, supply chain, regulatory affairs • Supporting the wider company in the maintenance and updating of documentation in accordance
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