QC

Method transfer of Pharmaceuticals Products and Materials. Analysis of In-process, Finished products and Stability study samples. Sampling and testing of Raw Materials, Packaging Materials and Water samples.

Candidate should be proficient in GLP. HPLC. GC. Instrumentation, Chemical Analysis, Raw Material Analysis, FG Analysis, UV, FTIR, In-Process Sample Analysis, and Stability Sample Analysis. 

Good analytical hand, well experienced in wet chemical analysis. Hands on experience of GC, HPLC, UV preferred. Aware of Good Manufacturing and Good Laboratory practices. Well versed with documentations related to a pharma laboratory.

M.Sc. / B.Pharma; review the latest pharmacopeial updates, supplements and amendments by evaluating the updates required in the available document to ensure the compliance with the current pharmacopoeia through consent with regulatory body

Experience in operating and cleaning a Vial Washing machine, Oepyrogenation Tunnel, Automatic Vial Filling and Sealing Machines, and Automatic PFS filling machines 

M.Pharm. QMS/AQA/IPQA/ Validation/Documentation. Candidates should have experience in Formulations regulated manufacturing company such as USFDA & MHRA. Exposure to regulatory audits like USFDA, MHRA is mandatory

B.Pharma / B.Sc; Trouble Shooter, Granulation, Compression, Coating, Machine Operators and Executives. Primary Packing, Secondary Packing. Hands on experience in HPLC, Chromatography Analyst, Trouble Shooting, and e-LIMS User, LCMS.

M.Sc, M. Pharma, B. Pharma. Analytical methods validation, verification and methods transfer. Validation of cleaning methods. Handling HPLC, GC, DR and other instruments. Preparing method validation verification protocol and report. Reviewing analytical hard copy and electronics data.

Environmental monitoring  Media fill visual inspection  Aseptic area monitoring  Handling of media fill activity  Aseptic area personal qualification