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3.0 - 5.0 years
3 - 3 Lacs
Hyderabad
Work from Office
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
2.0 - 3.0 years
3 - 3 Lacs
Hyderabad
Work from Office
Retrival& Issuance of documentation GDP CGMP Control Documents Dispatch verification Batch Manufacturing
Posted 1 week ago
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