25.04.24 | Vollzeit | Bern | Randstad Schweiz AGPeriodic reviews of equipment and systems. - Prepare, review, and approve technical and GMP-related documentation. - Coordinate FAT/SAT and commissioning activities for new systems. - Handle Change Controls, CAPAs, and Non-Conformances related to CSV. - Contribute to ensuring changes in systems
Später ansehen31.10.19 | Vollzeit | Bern | Decomplix' ISO 13485 quality management system. - supporting our customers in quality management. - customer support on their regulatory path (pre- and post-market). - project management to bring the technical documentation of customer products to the point where they can obtain the CE mark for medical devices
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