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.
- Positive communication and documentation skills.

Apply now if you have relevant QA documentation experience in the Pharmaceutical Manufacturing industry. - +91-XXXXXXXXXX

Pay: ₹30,000.00 - ₹50,000.00 per month

Work Location: In person

📌 QA Representative (Documentation / GMP Practices) - Pharma Company - Ahmedabad (India)
🏢 Gujarat Construction
📍 India