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Job DescriptionQC Chemist OTC & Personal Care Contract Manufacturing Full Time • Immediate Opening • Salary: Open (please include requirements with resume) We are a growing OTC contract manufacturer serving the pharmaceutical and personal care industry. This is a hands-on QC role at the center of our quality operation — you'll own analytical testing across the full product lifecycle, from incoming raw material through finished product and stability, with the autonomy to author SOPs and drive qualification projects. Position Responsibilities • Perform QC chemistry and analytical testing on incoming raw materials, • Conduct in-process and finished product testing; review batch records, • Perform product stability studies, • Conduct microbiological testing, • Perform water system testing and monitoring controls, • Execute IQ, OQ & PQ validation on equipment, including analytical instruments (spectrometers, etc.), • Perform routine calibration of laboratory instruments, • Calculate, record, and compile assay reports, • Author and revise QC chemistry SOPs, • Maintain laboratory cleanliness and organization, • Perform all work in accordance with cGMP and applicable FDA regulations Education • BA/BS degree with a major or minor in Chemistry Experience & Requirements • Minimum 3 years of experience in the pharmaceutical, OTC, or personal care industry, • Substantial hands-on experience with QC testing of bulk, final, and stability pharmaceutical products, • Demonstrated experience with water system testing and controls (required), • Solid working knowledge of cGMPs, FDA pharmaceutical regulations, and SOPs, • Familiarity with pharmaceutical manufacturing environments and processes, • Ability to work independently and collaboratively as part of a team, • Proficiency in Microsoft Word and Excel How to Apply Please submit your resume along with your salary requirements. This position is available immediately.

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