Mankind Pharma

Person should have the worked on Peptide Manufacturing & Peptide Synthesis and Exposure to Peptide Synthesis, purification, filtration and drying processes and Peptides synthesis, Peptide purification, Lyophilization.

Hands on Experience on Various QC instrument calibration like HPIC, GC, mil, Polarimeter. UV-Viyble Spectrophotometer, Dissolution etc.

Take responsibilities as Study Director for conduct of studies as per GLP principles / GMP guidelines.

Knowledge of HPLC / GC Empower software / UV, FTIR, Polarimetry, KFT, ATT, Balances, pH, Malvern PSD, PXRD instrument. Knowledge of GLP.

The candidate must be capable of analyzing raw materials, finished products, and stability samples. Knowledge of AMV and QAMS will be given preference.

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

M.Sc Chemistry, B.Pharm, M.Pharm ; Preparation of IPQA SOPs, IPQA Checks, AQL, Line Clearance, Review of BPR, Audit & Compliance, Sampling of API & Drug Product, Document & Data Control, Control Sample Management.

Candidate should be science Graduate having good communication skills.

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