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Responsible for chemical/physical analysis of raw materials, intermediates and finished products; and performing QC assays and comprehensive recording of laboratory test results. Adhering to all EPA, FDA, cGMP, cGLP DEA regulations and internal SOP's as they relate to the operation of the Quality Control lab and general operation of the chemical production facility;Following all OSHA and company safety rules and practices;Responsible for the review and documentation of all laboratory data and data entry;Performing a wide variety of chemical analyses for release of raw materials, in-process, intermediates and finished goods;Maintaining laboratory programs such as calibration/preventive maintenance, IQ/OQ/PQ (installation qualification, operational qualification, performance qualification) to test and calibrate analytical equipment; Performing in-depth laboratory investigations of non-complying test results;Writing controlled documents such as reports, test procedures, SOPs, etc;Evaluating validity of test results;Performing and document method transfer from Analytical Development;Running method evaluation experiments;Handling, analyzing and disposing of hazardous samples and waste;Maintaining laboratory solutions, inventory and notebooks;Assisting in training laboratory personnel as needed both inside and outside the department;Coordinating and communicating project status to the department manager; andServing as departmental subject matter expert (SME) to ensure comprehensive recording of test results, accuracy of laboratory data and adherence to cGMPs and all regulatory requirements. Bacheloris or equivalent in a Chemistry, Biochemistry, Pharmaceutical Sciences or a related field.3 years of experience in the job offered or in a QC role in the life sciences and/or pharmaceutical manufacturing industries.Must have:Three years of experience in a laboratory cGMP environment Working knowledge of analytical instrumentation;Strong chemistry theory;Effective verbal and written communication skills;