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Piramal Pharma Solutions

Quality Control Analyst

Piramal Pharma Solutions, New York, New York, United States

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Job Overview Performs Analytical chemistry examination testing on raw materials, finished products or stability samples in accordance with approved Standard Operating Procedures (SOPs) and valid methods. This is a safety-sensitive role.

Key Roles/Responsibilities Chemical or Physical testing analysis of raw materials, finished products, stability or request samples Documenting and submitting all raw data and results in LIMS Preparation of reagents for chemical analysis including peer review Knowledgeable in compendial (USP/EU) testing requirements and ensuring compliance per FDA 21 CFR

Experience Bachelor's degree in chemistry, biology, microbiology or other related science with relevant laboratory coursework is required. 1 - 2 years laboratory experience, preferably in a GMP environment

Competencies Basic knowledge of laboratory safety practices and PPE Basic knowledge of cGMP Basic understanding of good documentation practices Understanding of compendial testing requirements Preferred experience with FTIR, dissolution, UV-VIS, Karl Fischer, pH, wet chemistry techniques, reagent preparation, volumetric solutions.

Physical Requirements Lift/move up to 10 lbs. and occasionally 25 lbs. Individual may be required to handle hazardous and non-hazardous materials. Individual may be required to wear Personal Protective Equipment. Not allergic to chemicals or biosubstances found in the laboratory or production facilities.