QA senior Laboratory Specialist

vor 4 Wochen


CorsiersurVevey, Schweiz Randstad Vollzeit

Within the scope of a challenging, ambitious and future-oriented project driven by a dynamic team in an inspiring environment, we look for a QA laboratory equipment/system specialist.

Your Role :

· Define the laboratory equipment/systems quality strategy including data integrity aspects

· Review and approval of GxP documents, including URS, traceability matrix, risk assessments, systems drawings, procedures, qualification documents...

· Collaborate with the project teams to ensure that all the deliverables meet quality specifications

· Comply with all applicable health authorities regulations

· Comply with all applicable company standards

· Participate to risk assessments

qualifications

Who you are:

Minimum bachelor's degree in scientific studies At least 5 years of experience in a pharmaceutical/biotechnology environmentKnowledge in laboratory equipment and processesKnowledge in cGMP and health authority expectationsA proactive approach to all aspects of QualityGood communicator, dealing directly and efficiently with project teams and stakeholdersOrganized and logical in defining workload and delivering projectsFluent in English (written and spoken), French is a plus

  • Corsier-sur-Vevey, Schweiz Randstad Vollzeit

    Within the scope of a challenging, ambitious and future-oriented project driven by a dynamic team in an inspiring environment, we look for a QA laboratory equipment/system specialist.Your Role :· Define the laboratory equipment/systems quality strategy including data integrity aspects· Review and approval of GxP documents, including URS, traceability...


  • Corsier-sur-Vevey, Schweiz Randstad Vollzeit

    Within the scope of a challenging, ambitious and future-oriented project driven by a dynamic team in an inspiring environment, we look for a QA laboratory equipment/system specialist.Your Role :· Define the laboratory equipment/systems quality strategy including data integrity aspects· Review and approval of GxP documents, including URS, traceability...

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