26.04.24 | Vollzeit | Bern | Thermo Fisher ScientificAs a member of the Quality Control management team the position holder manages the Microbiology Unit (MBQC) at Thermo Fisher, Lengnau site according to project timelines and future routine demands. Your responsibilities Ensure the continued update of the operational procedures related to the QC area to align
Später ansehen25.04.24 | 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 AGRefractometry, Manual titrations, Conductivity, .) - Being responsible for raw material sampling, when the need arises - Write scientifically-sound technical documents and reports - Support laboratory management, e.g., planning activities covering end-to-end raw materials process - Support a timely
Später ansehen10.04.24 | Vollzeit | Bern | Randstad Schweiz AGdocuments like MBR, Work Instructions, Equipment manuals and Process Risk assessments - Writing of electronical Batch Records will be one of the main tasks at the beginning - Train Operators on written process documents - Support PPQ (Process Performance Qualification) - Managing of Quality Issues, Root
Später ansehen26.03.24 | Vollzeit | Bern | Randstad Schweiz AGCompliance with all applicable regulations, procedures and standards - Responsible for adherence to global and local project management processes - Responsible for document lifecycle within the assigned projects according to defined processes - Responsible for organizing day-to-day business of the assigned
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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