QC

Clinical batch data review, method validation, and stability study evaluations as per cGMP & regulatory norms. Routine analysis of clinical samples and stability samples. 

B.Pharm, M.Sc, B.Sc ; Hands on experience in LIMS,HPLC/FP Analysis.

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

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.

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

Biological E. Limited invites both experienced professionals and fresh diploma holders, as well as graduates and self-driven individuals.

Cadila Pharmaceuticals is an Indian multinational pharmaceutical company based in Ahmedabad.

Ipca Laboratories Limited Invites experienced, dynamic, and self motivated candidates. Protocol Preparation and Compilation Report of Process Validation, ANDA, Hold Time Study

B.Pharma, M.Pharma with 2 - 6 years of experience in Tablet, Capsule department with experience in Granulation, Compression, Coating, Inspection.