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 ansehen18.04.24 | Vollzeit | Bern | Randstad Schweiz AGAre required - Being responsible for completion (i.e., execution and documentation) of different analytical tests according to internal (TMDs) and/or external (e.g., EP, USP, ISO) requirements. Analytical tests encompass EP/USP ion ID tests, FTIR, TLC, Appearance of solution, pH, Osmolality, Density
Später ansehen06.03.24 | Vollzeit | Bern | Randstad Schweiz AGAnd approve technical and GMP related documentation (URS, impact/risk assessment, Master plans, qualification/validation documentation) - Understand customer needs and define electronic records requirements for computerized system adhering to regulation and company standards - Coordinate and execute FAT/SAT
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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