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QC Chemist I. Job in Allentown Gr8Jobs
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What they do
A Quality Control Chemist uses chemistry analysis to test samples of manufacturing or pharmaceutical products, to ensure that products meet quality standards.
$73,421 / year median in Pennsylvania
+5% projected growth
Job Description
B. Braun is seeking a QC Chemist I to support quality control testing of pharmaceutical and infusion therapy products. In this on-site lab role, you will perform routine and non-routine analytical testing of raw materials, in-process samples, and finished products using techniques such as HPLC, GC, and wet chemistry. You will ensure accurate documentation in compliance with GMP, FDA, and USP requirements, assist in investigations and method transfers, and collaborate with cross-functional teams. B. Braun offers a collaborative, learning-focused culture with strong opportunities for professional growth. Responsibilities Perform routine and non-routine analytical testing of pharmaceutical products and raw materials following GMP and SOPs Operate, calibrate, and maintain laboratory instruments such as HPLC, GC, UV-Vis, and p H meters Document all test results accurately in laboratory notebooks and electronic systems, ensuring data integrity Conduct stability, release, and validation testing to support production and regulatory submissions Interpret analytical data, troubleshoot out-of-specification results, and participate in investigations Prepare reagents, standards, and solutions in accordance with validated methods Collaborate with production, R D, and quality teams to resolve quality issues and support continuous improvement Ensure compliance with FDA, USP, and company quality standards and safety regulations Participate in method transfers, verifications, and equipment qualifications Contribute to a culture of safety, collaboration, and continuous learning within the QC laboratory Required Skills HPLC operation and troubleshooting Gas chromatography (GC) Analytical chemistry techniques (titration, spectroscopy, wet chemistry) GMP/GLP compliance and documentation Method validation and transfer support Data analysis and interpretation Laboratory equipment calibration and maintenance Stability and release testing Electronic laboratory systems (LIMS, ERP, or similar) Root cause analysis and deviation/investigation support