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 ansehen08.01.24 | Vollzeit | Bern | JobLeads GmbH | CHF 250’000 - CHF 300’000 In laboratory animal medicine LTK1, LTK2 and others as needed - Employment according to cantonal guidelines Send your fully documented application (CV, intention letter, at least two references) until October 7 th 2023 to n@ #J-18808-Ljbffr
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 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 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 ansehen30.08.22 | Vollzeit | Bern | Jobtic SAReputationMotivated personality who enjoys teamwork and challenges, and who likes to support colleagues and share knowledge and ideasPassion for cyber security and an interest in developing in a rapidly changing environmentAble to develop long-term solutions and document them
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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