11.04.24 | Vollzeit | Schaffhausen | Johnson & JohnsonAnd equipment. Quality investigation lead for major non-conformances (CAPA investigations)Review and approve Protocols, Reports, SOPs/WIs, Change requests (COCs) and other applicable documentsReview and approve GMP critical SAP master data (e.G. manufacturing instructions)Support ‚customers‘ (Production
Später ansehen19.04.24 | Vollzeit | Schaffhausen | Randstad Schweiz AGOf the leading pharmaceutical companies in Switzerland and at the same time a strategic launch and growth site. As a Quality Systems Documentation and Training Specialist you will join a diverse team and be responsible for administration of GMP documents and trainings at the Janssen Schaffhausen site and drive
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