Role & responsibilities
Robust knowledge of API manufacturing processes.
Experience in batch release management, ensuring compliance with regulatory and internal requirements.
Review of executed batch records, including audit trail review for data integrity compliance.
Preparation and review of Annual Product Reviews (APR) in line with regulatory expectations.
Preparation and review of Process Validation protocols and reports.
Review of technology transfer documents and data for completeness and compliance.
Initiation, review, and management of QMS elements such as Deviations, Change Controls, OOS, OOT, and CAPA.
Oversight of dispatch activities and line clearance to ensure compliance with GMP requirements.
Experience in cleaning validation, including protocol and report review.
Conducting internal audits and ensuring timely closure of audit observations





Preferred candidate profile
Robust experience in API manufacturing within a GMP-regulated environment
Hands-on experience in batch release, BMR/BPR review, and QMS management (Deviation, OOS, CAPA, Change Control)
Proven exposure to regulatory and customer audits (WHO/GMP, preferred) (USFDA/EMA)
Experience in validation, APR/PQR, stability studies, and technology transfer activities
Solid understanding of data integrity and risk assessment practices

Education UG: B.Pharma in Pharmaceutical, Pharmaceutical Chemistry

PG: M.Pharma in Pharmacy, MS/M.Sc(Science) in Chemistry

Job Type: Full-time

Pay: ₹45,000.00 - ₹80,000.00 per month

Work Location: In person

📌 Manager Quality Assurance / Reliance Rasayan Api Who Gmp Facility Gidc Naroda
🏢 Reliance Rasayan
📍 GIDC Naroda