QC Chemist | 7pm to 7:30am

Not Ready Important Notice About the Application Process This position offers use of our AI screening tool as part of the initial candidate review. While completing the AI screening is optional, please note: Candidates who complete the AI screening are reviewed first—daily. We strongly encourage you to complete it promptly to ensure early consideration (first come, first served). Expect to receive a prompt from our AI screener shortly after applying. The AI screener helps us streamline the Candidate intake process, but rest assured— you'll still work directly with a Masis recruiter throughout the rest of your hiring journey. QC Chemist $22-$24/hr. + 10% shift differential 7:00 PM - 7:30 AM | 2-2-3 schedule 6-month contract Join a FAST growing Pharmaceutical Manufacturing site supporting the production of Critical Care drug products in a GMP lab environment.

Job Summary:

Perform analytical testing of In-Process, Bulk, Stability and Finished Product to provide information about the quality, identity, purity, and safety of the material and provide decisions into the next steps in the manufacturing process.

Key Responsibilities:

Perform sample preparation and GMP testing of raw materials, in-process, bulk, stability, and finished product Operate and maintain analytical instruments (HPLC, GC, UV, FTIR, KF, ICP/MS, or AA) Complete GMP documentation in compliance with SOPs and data integrity requirements Support OOS, deviations, and lab investigations Prepare standards, solutions, and calibration activities Maintain lab logbooks, inventory, and stability samples Review analytical data and production records, including peer review Follow all GMP, safety, and quality procedures in a 12-hour shift environment

Job Requirements:

Must have at least 1 year of experience in a GMP laboratory setting. Familiar with GMP/GLP and FDA requirements. Strong documentation skills Familiar with SAP, OpenLab, Ensur, MS Office #MPG1

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