Job Description

Pharmaceuticals Industry is looking for an experienced QA skilled with 34 years of relevant experience in pharmaceutical manufacturing, particularly in Tablet and Liquid dosage-form units.

Key Responsibilities
Handle Quality Assurance activities for Tablet and Liquid manufacturing units.
• Review and maintain Batch Manufacturing Records (BMR) and Batch Packing Records (BPR).
• Ensure compliance with SOPs, GMP and applicable quality standards.
• Perform in-process and finished-product documentation review.
• Handle deviations, change controls, CAPA and investigations.
• Coordinate with Production, QC, Warehouse and other departments for QA-related activities.
• Ensure proper documentation and data integrity.
• Participate in internal audits and support regulatory/customer audits.
• Monitor compliance with approved procedures and manufacturing practices.
• Review and approve relevant manufacturing and quality documents.




• Support continuous improvement and quality-system activities.

Candidate Profile
34 years of relevant experience in Pharmaceutical Quality Assurance.
• Experience specifically in Tablet and Liquid dosage-form manufacturing is preferred.
• Valuable knowledge of GMP and pharmaceutical QA systems.
• Experience in documentation, BMR/BPR review, deviations, CAPA and change control.
• Valuable communication and coordination skills.
• Candidate should be willing to work at the manufacturing facility.

Qualification

B.Pharm / M.Pharm or relevant pharmaceutical qualification.

Salary

6.00 LPA to 7.20 LPA, depending on experience, skills and suitability.

Key Skills

Quality Assurance, QA, Pharmaceutical QA, GMP, Tablets, Liquid Manufacturing, BMR, BPR, SOP, CAPA, Deviation, Change Control, Audit, Documentation, Pharma Manufacturing.

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