15.09.24 | Vollzeit | Corsier-sur-Vevey | JobLeads GmbH | CHF 80’000 - CHF 100’000 Change initiatives to enhance safety protocols - Conduct EHS investigations and deliver effective EHS training programs - Maintain and monitor EHS permitting and regulatory compliance, ensuring all necessary documentation is up to date - Conduct and track workplace safety and compliance inspections
Später ansehen20.09.24 | Vollzeit | Corsier-sur-Vevey | Randstad Schweiz AGAnd/or approve qualification/validation documents, risk assessment, SOPs and take quality decisions according to company standards The activities of the QA Expert cover all qualification/validation phases from Basic Design until 1st use of equipment/raw material.10. You ensure GMP compliance during all phases
Später ansehen19.09.24 | Vollzeit | Corsier-sur-Vevey | Randstad Schweiz AGAnd reporting, to ensure the delivery of our specialty innovator Biotech pipeline to patients. Your Rôle - Contribute to the startup of high-tech analytical laboratories in the BDC by supporting procedure/document writing and analytical equipment for at least one of the following areas (e.g., for liquid
Später ansehen09.09.24 | Vollzeit | Corsier-sur-Vevey | Randstad Schweiz AGAnd documentation of project activities as required. Your Profile - Strong knowledge in biotechnological processes, detailed manufacturing operations (including automated & execution systems, engineering designs, P&ID, etc.), and new technologies. - Pragmatic, solution-oriented, and resilient with the ability
Später ansehen26.08.24 | Vollzeit | Corsier-sur-Vevey | Randstad Schweiz AGSampling, aliquoting, utility sampling, HVAC, Gases, corrections of working papers, ) - Perform support activities (autoclave and part washer) - Carrying out the documentation related to your function (e.g. writing working instructions) - Supporting compliance activities (batch review, deviations
Später ansehen23.08.24 | Vollzeit | Corsier-sur-Vevey | Randstad Schweiz AGPractices, registration product files and site quality standards. - To ensure that the documentation linked to the validation is done according to defined planning to support the establishment of the APR for the commercial and clinical molecule. - To highlight the potential project's issue from a pro-active
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