05.06.24 | Vollzeit | Aubonne | Randstad Schweiz AGRelated to change, risk and deviation management) - Support Equipment and Automated Systems deviation management. - Support, review and approve change control proposal (CCP) as QA engineering for projects - Participate to risk assessments - Review and approve quality documents (design documents
Später ansehen28.05.24 | Vollzeit | Bern | Randstad Schweiz AGPerform Technology Transfer of a new process into GMP Manufacturing (writing of Process relevant documents like Process Description, MBR's (first draft), WorkInstructions etc - Training of Operators on new - written documents - Writing of Reports (TechTransfer/Campaign), Technical documents like Risk
Später ansehen28.05.24 | Vollzeit | Bern | Randstad Schweiz AGTechnical documents like Risk Assessments - Technical Assessments - Help in troubleshooting and process improvements - Perform GEMBA walks in the Manufacturing suites - Managing of Quality Issues, Root Cause Analysis and Investigation - Data verification - Data trending - Initiating and implementing
Später ansehen28.05.24 | Vollzeit | Bern | Randstad Schweiz AGTechnical documents like Risk Assessments - Technical Assessments - Help in troubleshooting and process improvements - Perform GEMBA walks in the Manufacturing suites - Managing of Quality Issues, Root Cause Analysis and Investigation - Data verification - Data trending - Initiating and implementing
Später ansehen28.05.24 | Vollzeit | Gruyères | Randstad Schweiz AGParticipate to the global transfer strategy (write validation/verification plans, protocols and reports. Ensure the review) - Write analytical procedures, risk analyses and any other quality document, - Take part in activities related to lifecycle management, - Transfer analytical knowledge to the QC
Später ansehen28.05.24 | Vollzeit | Bern | Randstad Schweiz AGPerform Technology Transfer of a new process into GMP Manufacturing (writing of Process relevant documents like Process Description, MBR's (first draft), WorkInstructions etc - Training of Operators on new - written documents - Writing of Reports (TechTransfer/Campaign), Technical documents like Risk
Später ansehen27.05.24 | Vollzeit | Basel (Basel-Stadt) | Randstad Schweiz AGAnd processes within TR&D in Basel - Support of implementation of DI requirements - Review and approval of GMP relevant Documents like Plans, Reports, SOPs, Change Control, Discrepancy Management, CAPA (corrective action and preventive action), Risk Analysis - Assist management in regulatory inspections
Später ansehen27.05.24 | Vollzeit | Lausanne | Randstad Schweiz AGInfrastructure for one of our clients across dispersed sites in Switzerland; Ensuring change management processes are followed, documented and communicated; Working with Network Architecture teams to ensure the new model is in line with capacity requirements; Co-ordinating network migration activities (some
Später ansehen27.05.24 | Vollzeit | Basel (Basel-Stadt) | Randstad Schweiz AGFor our client, an international pharma company in Basel, we are looking for a QA Manager to support and oversee the end to end cGMP activities in implementation of Annex 1 requirements at the Clinical Supply Centre Basel. They take care that the Right to Operate can be maintained by ensuring
Später ansehen22.05.24 | Vollzeit | Lugano | Randstad Schweiz AGOttimizzazione dei processi produttivi e delle procedure di pulizia e di manutenzione - Stesura e revisione documentazione di reparto - Condurre il team di reparto in modo efficace e efficiente in linea con gli obiettivi aziendali. - Programmazione turni e orari di lavoro del reparto in base alla programmazione
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