Primary Responsibilities: Exposure for Analysis and documentation of tablets, capsules, Liquid/Cream. Developing and validating analytical test methods for the testing of pharmaceutical products for manufactured to GMP and ICH requirements. Developing and validation of Cleaning Method validation. Transferring and documentation new analytical techniques to the Quality Control (QC) laboratory. Controlling laboratory chemicals required for analytical activities. Planning and organizing stability testing. Writing/reviewing specifications and methods of analysis. Writing/reviewing of Standard Operating Procedures (SOPs) as per regulatory requirement. Participating in self-inspections and regulatory inspections. Sample management and Documentation of RM and PM. Preparation and review of all analytical related documents. Working standard management. Handling of QC Instrument operation and Calibration related activity. Handling of OOS / OOT and Lab related incident / Investigation. Planning of daily activities of the laboratory.Desired Skills, Qualifications & Experience: B.Pharm, M.Pharm/ M.Sc. 2-4 years of experience.Job Types: Full-time, Regular / PermanentSalary: ?10,000.00 - ?15,000.00 per monthSchedule:
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