We are looking for a QA Executive / Sr. Executive (2–5 years) to manage Quality Assurance, QMS, batch documentation, and customer/production quality coordination for our pharmaceutical third-party manufacturing operations.

Key Responsibilities

- Review BMR & BPR for completeness, accuracy, compliance, and GDP.
- Review MFR, specifications, COA, analytical reports, and other batch-related documents.
- Ensure compliance with GMP, GDP, WHO-GMP & Schedule M requirements.
- Manage and maintain export documentation and records.
- Coordinate with marketing partners regarding quality documents, specifications, COA, complaints, and other QA requirements.
- Support customer audits, regulatory audits, vendor qualification, and quality documentation.
- Coordinate and support domestic and export customer audits/visits, ensuring readiness, compliance, documentation, and timely closure of audit observations.




- Ensure timely closure and proper documentation of quality observations and discrepancies.
- Maintain strong control over product-wise, batch-wise, and customer-wise documentation.

Requirements

- 2–5 years of experience in Pharmaceutical QA / QMS / Documentation.
- B.Pharm / M.Pharm / M.Sc.
- Strong hands-on experience in BMR/BPR review and pharmaceutical documentation
- Solid documentation, communication, coordination, and follow-up skills.
- Experience in third-party pharmaceutical manufacturing will be preferred.

Pay: ₹15,551.84 - ₹30,305.26 per month

Benefits:

- Flexible schedule
- Health insurance
- Leave encashment
- Provident Fund

Experience:

- QA Executive: 2 years (Required)

Work Location: In person

📌 QA Officer-Quality Assurance & Third-Party Operations (India)
🏢 MGA DRUGS
📍 India