QA Assistant

Assist in preparation, review, issuance, and control of SOPs and other quality documents.

Maintain and control QA documentation, including records, registers, and document logs.

Review Batch Manufacturing Records (BMR) and Batch Packing Records (BPR), as applicable.

Ensure compliance with GMP, GLP, GDP, and applicable pharmaceutical quality requirements.

Assist in handling deviations, change controls, CAPA, and incident documentation.

Maintain training records and coordinate GMP training for employees.

Support internal audits, external audits, and regulatory inspections.

Ensure proper documentation practices and compliance with data integrity requirements.

Coordinate with QC, Production, Engineering, and other departments for quality-related activities.

Pay: ₹250,000.00 - ₹400,000.00 per year

Benefits:

• Provident Fund

Work Location: In person