1 - 3 years
1 - 4 Lacs
Posted:2 months ago|
Platform:
Work from Office
Full Time
Roles and Responsibilities Ensure compliance with cGMP guidelines during documentation, cleaning validation, equipment qualification, process validation, and OSD operations. Conduct BMR reviews, BPR reviews, change controls, deviation management, CAPA implementation, and market complaint handling. Perform QMS activities such as document issuance, master planning, batch manufacturing record review, stability analysis reports preparation. Maintain accurate records of quality systems including logbooks and protocols. Collaborate with cross-functional teams to resolve quality issues and implement corrective actions.
Finecure Pharmaceuticals
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My Connections Finecure Pharmaceuticals
1.5 - 4.25 Lacs P.A.