QC

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

Responsible for BET, MLT, and sterility testing with method validation and investigations, ensuring GLP/GMP compliance, accurate documentation, and equipment adherence.

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

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

Capsule filling / Compression / Coating process area Supervision, Documentation, USFDA Compliance.

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

Must have knowledge of preparation and execution of SOP, manufacturing. Packing and qualification document of SCADA based equipment.

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