B.Sc

In-process checks, Line clearance, batch record review, GMP compliance, shop floor monitoring, process validation

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

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

1st Class Post Graduate Degree, including the integrated PG Degree in Biotechnology, Life Sciences/Applied Biology / Life Sciences OR Second Class Post Graduate degree including the integrated PG degrees in Sciences with Ph.D. in Biotechnology / Life Sciences / Applied Biology 

Strong background in Chemistry, Life Sciences, Environmental Science, Instrumentation, data acquisition systems and computers. Ability to handle repairing and maintenance work of the instruments.