4-5

Panacea Biotec, To maintain cGLP in Quality Control Laboratory. To prepare HVAC / compressed air / effectiveness of cleaning validation planner. To ensure to do proper API calculation before dispensing as per formula.

B.Pharm / M.Pharm (Pharmaceutics / Pharmaceutical Technology) with 2-8 years of experience in technology transfer.

Compression, Coating, Granulation, Inspection, Capsule filling. Blister Packing / Bottle Packing

Perform sample preparation, extraction, and analysis using techniques such as HPLC , GC-MS, LC-MS, ICP MS , ICP OES and other relevant instrumentation.

Having Injectable Experience of Analytical Method Validation for Assay, Related Substances Content by HPLC and Residual Solvents by CC, Preparation and Review of Method Validation and Method Equivalency and Method Transfer Protocols and Reports.

Supervise production lines, including Granulation, Compression, Coating, and Packing. Good verbal and written English communication skills

Hands on Experience on, Stability Studies, Analytical Method Validation & Finished Goods.

Experience in review of HPLC, GC, LCMS calibration data & Analytical Data review &Review of Analytical Method Validations, Method Transfers, Protocols & Reports.

Able to perform Biochemical techniques, Chromatography techniques, Electrophoresis techniques, Immuno assay techniques, Cell culture techniques and Molecular techniques