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Process Validation Engineer Fusion Life Sciences Technologies

8.0 - 10.0 years

9 - 11 Lacs

pune

Work from Office

Responsibilities: Ensure validation activities align with FDA 21 CFR Part 820 , ISO 13485 , ISO 14971 and Philips QMS. * Conduct risk assessments and FMEAs * Collaborate on CAPA implementation and RCA investigations. 21 CFR 820 , ISO 13485 , GMP , and QSR

Posted 20 hours ago

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