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.
Ipca Laboratories Limited Invites experienced, dynamic, and self motivated candidates. Protocol Preparation and Compilation Report of Process Validation, ANDA, Hold Time Study
Post-Graduation in life science. Graduate degree in science with PG Diploma in Clinical Research. Experience of one year in relevant filed is desirable.