Quality Control Analyst at Integrated Resources, Inc. | Cincinnati

Position: Quality Control AnalystLocation: Cincinnati, Ohio 45213Duration: 4+ months (with potential for extension)Key Responsibilities:Possess a Bachelor’s degree or higher in a science-related field; a background in chemistry is highly desirable.Have at least 1 year of relevant experience in an FDA-regulated setting.Conduct routine chemical testing of raw materials and packaging components, adhering to USP or in-house methodologies.Perform qualitative and quantitative analyses utilizing advanced analytical instrumentation.Employ electronic laboratory information systems such as LIMS for efficient data processing.Evaluate data against established specifications, promptly informing management of any out-of-specification (OOS) results or anomalies.Conduct peer reviews of laboratory test results as necessary.Maintain comprehensive laboratory records in compliance with Good Manufacturing Practices (GMP).Must be capable of standing for extended periods throughout the workday.Ability to lift up to 20 lbs on an occasional basis is required.

Hold a Bachelor’s degree or higher in a science-related field, with a preference for chemistry.Possess a minimum of 3 years of relevant experience in a pharmaceutical environment.Conduct analyses, inspections, and tests on products, raw materials, in-process materials, packaging materials, and quantitative assays on samples to guarantee that quality standards align with company policies, customer expectations, and regulatory compliance.Execute a variety of qualitative tests and assays utilizing equipment ranging from standard analytical tools to advanced automated instrumentation, while assisting in the maintenance and certification of testing apparatus to ensure compliance.Perform essential inspections, checks, analyses, and documentation of studies.Compile and oversee quality statistics and reports.Utilize analytical instrumentation such as HPLC, GC, UV/Vis, KF, and FTIR for qualitative and quantitative analyses.Employ electronic laboratory information systems such as LIMS and Empower for data acquisition and processing.Have a foundational understanding of USP, cGMP, and FDA regulations.Demonstrate knowledge and experience within the field while still acquiring advanced skills and knowledge.Address a range of straightforward problems effectively.Analyze potential solutions using established procedures.Receive moderate guidance and direction in responsibilities.

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