| Description | • Perform sampling and analysis of Raw materials, and packaging materials, and analysis of bulk products. • Prepare the reagents required for analysis. • Prepare and standardize the volumetric solutions according to the specification. • Record all results of analysis in the logbook. • Perform and record calibration of instruments as required. • Cooperate with lab staff. • Prepare the SOP’s, instructions, and calibration manuals. • Perform the necessary validation if required. • Perform stability studies when required according to stability schedule. • Maintain all instruments whenever and wherever possible, with or without the aid of instrumental agent. • Prevention and precautions against, or adequate control of, exposure to hazardous substances, and danger from flammable, explosive, electrical risks. • Liaison as necessary with all relevant authorities, and assistance and cooperation concerning audits and remedial actions that may be necessary. • Develop personal skills and capability through ongoing training, as provided by the company or elsewhere subject to Company approval. • Report as necessary any changes that may affect the quality of the product |
| Qualifications | o Pharmacist. o Min 2 yrs experience in Pharma Industry, chemistry instrumental analysis (Including HPLC, UV, Dissolution, IR, Karl Fischer, etc…). o Min 2 years experience in microbiology (could be an alternate to the chemistry background). |
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