Job Description

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