QC

Handle, supervise the manufacturing process and related activities of Compounding, Dosing section & Packing

Centaurs USFDA and MHRA approved plant is seeking deserving candidates having experience working in Oral Solid Dosage Manufacturing facilities for regulatory markets.

B.Pharm / M.Pharm. Responsible for Review of the batch manufacturing Record & Line clearance for OSD Area. Monitoring packing stability Batches, Zenotech

M.Pharm, B.Pharm, M.Sc, B.Sc. Experience in Granulation, Compression, Coating, capsule fiiling, Liquid Manufacturing, packaging.

Hands-on experience in batch operations, GMP documentation, shift handling, and operation of equipment like reactors, centrifuges, and dryers.

M.Sc./B. Pharma Fresher Pass out 2024 and 2025 openings for reputed college with good CGPA and communication skill.

MSc / B.Pharmacy ; 9-12 years of experience in FG/ Stability/PM / GLP / Micro /D0C-QMS

Knowledge of QMS & compliance, qualification & validation, aseptic core monitoring and IPQA.

To Review, check the method validations data as per the USP 1225– Validation of Compendial methods, ICH-Q2 guidelines for validation of analytical procedures, ANVISA, ORA-LAB, SOP and method of analysis.