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3.0 - 5.0 years

3 - 3 Lacs

Hyderabad

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Naukri logo

Responsible for maintaining and improving the Quality Management System (QMS) in compliance with ISO 13485:2016 and Local regulatory requirements (Indian Medical Device Rule). Responsible for internal audits, CAPA, change control, document control, risk management, and management review processes. Support external audits/inspections (Notified Body, regulatory, customer). Ensure compliance with applicable regulatory requirements and support quality system documentation updates. Collaborate with cross-functional teams to ensure quality and compliance across product lifecycle stages.

Posted 1 day ago

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2.0 - 3.0 years

3 - 3 Lacs

Hyderabad

Work from Office

Naukri logo

Retrival& Issuance of documentation GDP CGMP Control Documents Dispatch verification Batch Manufacturing

Posted 1 week ago

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