23.05.24 | Vollzeit | Bern | Bavarian Nordic Berna GmbHAnd approves process validation documents including risk assessmentsOversees site manufacturing activities (oral and parenteral) concerning sterility assuranceOwns the Contamination Control Strategy documents of the siteEstablishes annual Product Quality ReviewsEstablishes and approves trend reportsEnsures
Später ansehen30.04.24 | Vollzeit | Thörishaus | Bavarian Nordic Berna GmbHAnd approves process validation documents including risk assessmentsOversees site manufacturing activities (oral and parenteral) concerning sterility assuranceOwns the Contamination Control Strategy documents of the siteEstablishes annual Product Quality ReviewsEstablishes and approves trend reportsEnsures
Später ansehen25.03.24 | Vollzeit | Thörishaus | Bavarian Nordic Berna GmbHYour responsibilitiesResponsible, as QA representative in multidisciplinary teams, to oversee and review/approve qualification/validation documents and risk assessments for the following topicsQualification of Equipment, Facilities, UtilitiesComputer System Validation (CSV)In this role the QA
Später ansehen16.05.24 | Vollzeit | Bern | Randstad Schweiz AGApplicable regulations, procedures, and standards - Adhere to global and local project management processes - Document project activities according to defined processes - Organize day-to-day business of project resources/teams - Resolve technical issues within project scope including troubleshooting, root
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 ansehen10.05.24 | Vollzeit | Schlieren | jobwinner.chIn this multifaceted challenge? Then we look forward to getting to know you! Please apply online or send you application documents to Fritz Studer AG Natascha Saner* Postfach 177 3602
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 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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