4-5

Exposure of analysis for Finished Products, Stability Samples and Raw Materials. Having Knowledge of Analytical Method Validation, Verification and Method Transfer. Having skill for data interpretation, troubleshooting. Pharma knowledge of Solid orals and Quality process.

Walk-in Drive in pharmaceutical Production for B.Pharmacy, M.Pharmacy / M. Sc

Hands-on experience of different chromatography modes like RP, H1C IEX, SEC, etc is required. 

Understanding of Analytical Techniques, Review skills of BAR Batch analytical record. Incidents, Change control, OOS and CAPA.

M.Pharm, B.Pharm, M.Sc ; 2 to 8 Years of Experience in Analytical Compliance, Cleaning Sampling, RA Co-Ordination, Process Validation, QMS, Training Co-Ordination.

Perform line clearance, in-process checks, and timely documentation. Responsibilities also include analytical QA oversight, GMP monitoring. APQR and CVP execution, and maintaining data integrity and compliance across all functions.

Line clearance activity for Washing, Filling, Sealing, Visual inspection. Performing Environmental monitoring activity in Grade A, B, C and D clean room area. In process activity.

Knowledge of production activities. Verification of area, maintaining the record. Verification and dispensing of Raw material

Preparation, review and submission of Dossiers. Good exposure on Life Cycle Management. Handling Post approval & Pre approval