B.Pharm

Knowledge of Documentation, QMS, Deviation, Change Control, market Complaint, 00S, 00T, Validation Qualification, IPQA, Audit Compliance.

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.

To ensure the compliance of internal/ external audit and to ensure timely adequate response of audit finding from the department to the auditor to close the issue.

To have an oversight on CRO partners for outsourced studies by conducting oversight quality visits at sites if applicable, conduct regular meetings and seek regular updates on study progress.

Masters Degree / PG Diploma in Life Sciences / Biomedical Sciences / Pharmacy / Public Health / Clinical Research with experience in clinical project management and/or clinical trial/ study monitoring.

Concord Biotech Limited is a R&D driven biopharma Company. Fresher Having Qualification MSC / B.Pharm and M.Pharm

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

B.Pharma/M.Pharma Candidates with experience in injectable formulations and USFDA background will be given preference. Abryl Laboratories