Qms Executive

Cadila Pharmaceuticals

4 - 7 years

4 - 7 Lacs

ankleshwar

Posted:2 months ago| Platform:

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Skills Required

qms system documentation sop cgmp gmp compliance

Work Mode

Work from Office

Job Type

Full Time

Job Description

Key Responsibilities:

Prepare, review, and maintain Batch Manufacturing Records (BMR) / Batch Packing Records (BPR).
Ensure compliance with QMS activities Deviations, Change Controls, CAPA, and Incident handling.
Draft, review, and implement SOPs in alignment with regulatory and cGMP requirements.
Maintain production-related documentation in compliance with audit and regulatory standards.
Coordinate with QA, QC, and other departments for documentation and compliance activities.
Support in production planning, line clearance, and shop floor compliance.
Ensure adherence to GMP/cGMP guidelines and company policies.

Key Skills Required:

Strong knowledge of QMS and Documentation practices.
Understanding of cGMP, regulatory guidelines, and compliance requirements.
Experience in SOP preparation, BMR/BPR review.
Good knowledge of audit preparation & regulatory compliance.
Attention to detail with strong documentation and commu nication skills.

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