14.04.2025 | Full-time | Oradea | CelesticaThat are consistent with the Celestica standards and the industry validation frameworks and principles (ex GAMP 5, FDA CSA). Applies regulatory requirements and standards to systems, processes, and projects (ex FDA Parts 11/, EU GMP/MDR, ISO /). Supports validation projects that use Software Development Life Cycle
Uita-te mai târziu19.03.2019 | Full-time | Oradea | SalesConsulting | Management and execution of Quality-related elements of supplier management activities, inclusive of; incoming inspection processes, supplier qualification, supplier monitoring, etc. Planning and execution of supplier audit and corrective action activities related to both initial qualification and on-going
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