QA

Experience to perform analysis on HPLC instrument for raw material, Finished Products, In Process Sample.

Experience in QC Planning, Trackwise, AMV, Review, OOS, OOT, QMS, LIMS, CAPA, QMS and Risk Assessment QC Analyst (Micro)

Strong understanding of regulatory guidelines and documentation practices. Detail-oriented with excellent analytical and communication skills.

B. Sc / M. Sc. (Organic Chemistry I Analytical Chemistry) B.Pharmacy / M. Pharmacy 

Invite passionate professionals to join India's No. 1 pharmaceutical company and help deliver medicines that change lives worldwide.

MPharm, M.Sc, BPharm, B.Tech. DPharma, Diploma Candidates with regulatory plant exposure may apply.

Responsible for managing QMS activities including deviations, change control, CAPA, and OOS/OOT, ensuring timely closure and compliance with GMP and data integrity standards.

CIRO Pharma Private Limited plant at Biotech Park Phase III is aimed at manufacturing of Anti-Cancer Drugs for regulatory markets like the U.S.A, U.K, Europe, Canada, and South America.

INTERVIEW for M.Pharm, B.Pharm, M.Sc, B.Sc. Knowledge of Injectable plant in IPQA, GLR QMS, Validation, Vendor qualification, Audit Compliance