QA Representative (Documentation / GMP Practices) - Pharma Company - Ahmedabad

Job Title: QA Representative – Documentation / GMP Practices

Location: Jagatpur, Ahmedabad, Gujarat

Qualification: B.Pharm / M.Pharm

Experience: 3–5 Years

Industry: Pharmaceutical Manufacturing

Working Days: Monday to Saturday
Job Summary

We are seeking a QA Representative with 3–5 years of experience in the Pharmaceutical Manufacturing industry. The ideal candidate should have strong knowledge of GMP practices, quality systems, and documentation.
Key Responsibilities:
• Manage and maintain Quality Management System (QMS) documentation.
• Handle CAPA, Change Control, and Deviation processes.
• Support Process Validation (PV) and Equipment Qualification activities.
• Prepare and maintain product stability documentation for R&D and commercial batches.
• Review Batch Manufacturing Records (BMR) for accuracy and GMP compliance.
• Ensure compliance with GMP, SOPs, and regulatory requirements.
• Coordinate with cross-functional teams to maintain quality standards.

Required Skills:
• Strong knowledge of GMP and pharmaceutical quality systems.
• Experience in QMS, CAPA, Change Control, Deviations, PV, and Equipment Qualification.
• Hands-on experience in documentation and BMR review.
• Good communication and documentation skills.

Apply now if you have relevant QA documentation experience in the Pharmaceutical Manufacturing industry. - 9377165778
Pay: ₹30,000.00 - ₹50,000.00 per month
Work Location: In person