22.05.24 | Vollzeit | Bern | Randstad Schweiz AGOf process documents - Support the GMP-compliant production of active ingredients and drugs for clinical trials and market launch - Support Product MBR review - Support QA oversight for aseptic processing - Review and approval of non-conformities, CAPAs, and Effectiveness Checks - Ensure the relevancy
Später ansehen22.05.24 | Vollzeit | Bern | Randstad Schweiz AGCollecting and evaluating of data etc.) - Writing/Updating of technical reports and documents - Perform laboratory duties to support department objectives - Periodic review and evaluation of
Später ansehen22.05.24 | 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 ansehen22.05.24 | 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 ansehen22.05.24 | 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 ansehen16.05.24 | Vollzeit | Bern | Randstad Schweiz AGTechnicians, teams and departments. - Helping that master data and new data match the life cycle data. - Helping on any quality tasks but not limited to - CAPA documentation support - Non Conformance documentation support - Audit action support - Quality database support - Keep track on lead times
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 ansehen16.05.24 | Vollzeit | Bern | Randstad Schweiz AGControl department - Perform and/or support the writing of specification documents (URS) - Review test protocols, plans and reports - Support test execution - Support and train team members in CSV methodology - Supporting the timely and effective completion of investigations, change controls and CAPA’s
Später ansehen07.05.24 | Vollzeit | Bern | Randstad Schweiz AGVerification, functional testing, and documentation of results for QC equipment. - Work closely with cross-functional teams to coordinate and integrate equipment qualification activities within project timelines. - Identify and mitigate risks during the qualification phase, ensuring compliance with regulatory
Später ansehen07.05.24 | Vollzeit | Bern | Randstad Schweiz AGAnd requirements set by regulatory authorities. - Write/review Commissioning & Qualification plans and reports. - Execution of RQ, IQ, OQ including protocol deviations, investigation, and corrective action activities - Plan and track execution of commissioning & qualification activities/documentation versus
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