Kelly Science, Engineering, Technology & Telecom
Associate Scientist, Analytical Quality Control
Kelly Science, Engineering, Technology & Telecom, Cleveland, Ohio, us, 44101
Overview
Associate Scientist, Analytical Quality Control Responsibilities
Perform routine HPLC and GC analysis in a GMP API analytical laboratory Perform GMP analytical method transfers, assist in the preparation of transfer protocols and reports May also perform FTIR, IC, KF, XRD, NMR, DSC, TGA, particle size, titrations, UV-vis, optical rotation, and other analyses Coordinate release testing of raw materials, intermediates, APIs Perform investigations for out of specification data Coordinate the timely and compliant generation of data to support project timelines Review data for technical content and good documentation practices Other duties as assigned Education and Qualifications
Minimum B.S. in chemistry with 5+ years related pharmaceutical analytical laboratory experience or equivalent combination of education and experience is required. Relevant experience in good laboratory/manufacturing practices (GLP/cGMP), laboratory quality control or stability, and interaction with quality assurance is required. Specific Skills and Requirements
Experience with HPLC and GC analysis Experience with standard lab equipment (balances, pipettes, pH meter, etc.) Proficiency in Microsoft Excel and Word Possess basic chemistry knowledge and be able to handle laboratory materials safely Must be able to communicate effectively with technical, production, and quality personnel Must be able to effectively multitask Seniority level
Associate Employment type
Full-time Job function
Science, Quality Assurance, and Analyst Industries
Pharmaceutical Manufacturing
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Associate Scientist, Analytical Quality Control Responsibilities
Perform routine HPLC and GC analysis in a GMP API analytical laboratory Perform GMP analytical method transfers, assist in the preparation of transfer protocols and reports May also perform FTIR, IC, KF, XRD, NMR, DSC, TGA, particle size, titrations, UV-vis, optical rotation, and other analyses Coordinate release testing of raw materials, intermediates, APIs Perform investigations for out of specification data Coordinate the timely and compliant generation of data to support project timelines Review data for technical content and good documentation practices Other duties as assigned Education and Qualifications
Minimum B.S. in chemistry with 5+ years related pharmaceutical analytical laboratory experience or equivalent combination of education and experience is required. Relevant experience in good laboratory/manufacturing practices (GLP/cGMP), laboratory quality control or stability, and interaction with quality assurance is required. Specific Skills and Requirements
Experience with HPLC and GC analysis Experience with standard lab equipment (balances, pipettes, pH meter, etc.) Proficiency in Microsoft Excel and Word Possess basic chemistry knowledge and be able to handle laboratory materials safely Must be able to communicate effectively with technical, production, and quality personnel Must be able to effectively multitask Seniority level
Associate Employment type
Full-time Job function
Science, Quality Assurance, and Analyst Industries
Pharmaceutical Manufacturing
#J-18808-Ljbffr