- Conduct Analysis in compliance with cGMP requirements, compendia standards, and internal procedures Maintain accurate record of analysis and perform documentation to company standards
- Prepare test solutions, volumetric solutions, and samples used in analysis
- Performs assigned sampling, physical, chemical tests and assay on raw materials, active pharmaceutical ingredients, in-process, finished, and stability products analysis in an FDA regulated lab environment
- Uses a variety of analytical instruments such as HPLC, GC, Dissolution, Malvern, IR, Auto Titrator, UV Spectrophotometer, Dissolution, Karl Fisher (KF), Potentiometer etc.
- Perform analysis with a practical understanding of the test procedure and instrument operation
- Perform laboratory analysis right first time, contemporaneous documentation, analyze and document the results
- Conducts laboratory investigation under the supervision of laboratory manager.
- Performs maintenance and calibrations of laboratory instruments /equipment
- Complies with all regulatory/ in-house requirements may include but not be limited to safety, housekeeping, laboratory chemical waste, cGMP, cGLP, documentation
- Perform analysis with a practical understanding of the test procedure and instrument operation
- Maintain required level of training needed to perform a GMP task
- Prepares and/or Reviews Test Procedures, SOP's and Protocols as assigned
- Notify manager immediately of nonconforming data or unexpected occurrences
- Organize work schedule to complete assigned tasks efficiently and on schedule Work under direction provided by supervisor and Other duties as assigned
Job Type: Full-time
Pay: ₹11,481.93 - ₹25,000.00 per month
Work Location: In person
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