QA

Evaluate change control requests and assess their impact on product stability. Review laboratory test results (CoAs), investigate OOS/OOT findings, and prepare non¬conformity reports.

BDR Group of companies has grown steadily and become a house-hold name in the pharmaceutical Industry over the last 15 years, in both domestic and international arenas

The ideal candidate must have hands-on experience in ophthalmic formulations, along with strong expertise in autoclave handling and batch manufacturing processes. Knowledge of GMP and quality compliance is essential.

RPG LIFE SCIENCES LIMITED, ARE INVITING CANDIDATURE FROM PROFESSIONALS FOR BELOW MENTIONED POSITIONS

Responsible for development, optimization, and scale-up of tablet formulations, ensuring product quality, stability, and regulatory compliance.

B.Pharm / M.Pharm; Experience in Market Complaint / Investigation / Audit Compliance / Cleaning Validation / Process Validation. Micro Labs Limited

Preparation and control of SOPs, STPs, specifications, formats, and master documents. Review of BMR, BPR, deviations, change controls, and CAPA records. CLAPS Industries require QA Documentation professional

Akums Plant 1 specializes in the production of Oral Solid Dosage Forms, including tablets and capsules.

Oversee IPQA activities during injectable manufacturing & packaging Review and approve BMR/BPR ensuring cGMP compliance Handle deviations, CAPA, and audit readiness (QMS) Lead QA team activities and drive continuous improvement initiatives