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We are seeking a QC Chemist to join our growing team. The QC Chemist performs routine and non-routine chemical analyses of raw materials, in-process samples, and finished products to ensure product quality and regulatory compliance. This role supports production troubleshooting, laboratory operations, and continuous improvement activities within the Quality Control function. Primary Responsibilities • Perform qualitative and quantitative chemical analysis using techniques such as GC-MS, LC, FTIR, UV-Vis, Rheology, Particle Size Analysis, Spectrophotometry, titration, wet chemistry, and basic microbiological testing., • Conduct method validations, verifications, and transfers as assigned., • Execute testing of raw materials, intermediates, finished goods, and stability samples according to established methods, SOPs, and regulatory requirements., • Review, interpret, and document analytical data clearly and accurately in laboratory notebooks and electronic data systems., • Support investigations of OOS (Out-of-Specification) and OOT (Out-of-Trend) results, including root cause analysis and CAPA activities., • Make material disposition decisions (Approve / Reject / Rework) based on analytical results., • Calibrate and maintain laboratory equipment in alignment with internal procedures., • Ensure testing activities adhere to cGMP, GLP, and applicable quality standards., • Train and mentor junior laboratory staff as required., • Assist in preparing for internal and external audits, providing data and documentation., • Support preparation and revision of SOPs, test methods, and laboratory records., • Maintain a safe, organized, and compliant laboratory environment., • Perform additional related duties as needed. Minimum Requirements • 4–5+ years of experience in a Quality Control or Analytical Laboratory environment (required)., • Bachelor’s degree in Chemistry, Biochemistry, or related scientific field (required); Master’s degree preferred., • Experience in cGMP-regulated manufacturing environments (cosmetics, pharmaceuticals, chemicals, food science, or nutraceuticals)., • Solid understanding of cGMP, GLP, and regulatory documentation standards., • Experience with LIMS or other electronic laboratory data systems (preferred). Knowledge, Skills, & Abilities • Strong analytical, problem-solving, and troubleshooting skills., • Excellent documentation accuracy and attention to detail., • Clear written and verbal communication skills., • Ability to prioritize and manage multiple tasks in a fast-paced environment., • Collaborative work style with strong interpersonal skills., • Proficiency in Microsoft Office (Excel, Word, Outlook, Teams) and general data analysis.