20.06.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalInspection Process You will ensure Compliance with Takeda Quality Management System, regulations and standards, manage Compliance Risk Assessments and represnet your department during regulatory inspections. Ensure the oversite of Quality Systems Pocesses. You will lead a permanent Inspection ready status
Später ansehen19.06.24 | 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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