19.06.24 | Vollzeit | Neuchâtel | NonStop Consulting | Be instrumental in the production of active pharmaceutical substances, ensuring topnotch quality and efficiency. Key Responsibilities - Adherence to Standards Ensure compliance with cGMP, BDP, and EHS guidelines. - Process Execution Perform routine and nonroutine manufacturing activities. - Problem Reporting
Später ansehen14.05.24 | Vollzeit | Neuchâtel | Randstad Schweiz AG% - Working hours standard This resource will be specifically responsible for the following tasks - Review deviations in the framework of engineering events within quality systems (i.e. Trackwise) to verify acceptability and adherence to standard procedures and regulatory requirements. This includes
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