QA Analytical Chemist I
13 days ago
Torrance
Job Description TEMP-TO-HIRE OPPORTUNITY Job Description The Quality Control Analytical Chemist I supports quality operations by performing analytical testing on raw materials, in-process samples, and finished goods within a regulated manufacturing environment. This role ensures product quality and compliance with GMP and FDA standards through accurate testing, documentation, and participation in quality systems such as CAPA, deviations, and stability programs. The position collaborates cross-functionally to support continuous improvement and regulatory compliance initiatives. Pay $25.00 - $28.00 Schedule 10:00AM - 6:30PM or 12:00PM - 8:30PM (Training on 1st shift schedule with 7:00AM/8:00AM start) Job Duties • Analyze raw materials, in-process samples, and finished goods to determine chemical and physical properties, • Perform routine review of QC test data, including in-process, finished goods, and stability samples, • Document all testing results accurately and in accordance with established procedures, • Prepare standards and specifications for processes, products, and testing methods, • Participate in daily and weekly meetings, providing updates and escalating issues as needed, • Support root cause analysis and CAPA activities related to deviations, out-of-spec results, and complaints, • Assist in managing and improving the stability program, including protocols, testing schedules, and reporting, • Perform and support analytical testing methods (pH, viscosity, moisture, titration, FTIR, etc.), • Contribute to method development, qualification, and tech transfer activities, • Assist in laboratory investigations and deviation management, • Develop, review, and implement SOPs to ensure GMP and regulatory compliance, • Monitor and trend QC data across raw materials, in-process, finished goods, and stability samples, • Support audits and ensure QC lab compliance with GMP and regulatory requirements, • Collaborate with cross-functional teams to drive continuous improvement initiatives Requirements • Bachelor’s degree in Chemistry, Biology, Pharmaceutical Sciences, or related field, • Minimum 3+ years of experience in a QC laboratory or regulated manufacturing environment preferred, • Experience in cosmetics or OTC manufacturing strongly preferred, • Working knowledge of GMP, FDA regulations, and quality systems (21 CFR Part 11, 210, 211), • Experience with analytical testing methods (organoleptic, viscosity, pH, moisture, specific gravity, titration, FTIR), • Experience with method development, validation/qualification, and tech transfer, • Strong understanding of deviations, investigations, and CAPA processes, • Proficiency in Microsoft Office (Word, Excel, PowerPoint), • Strong attention to detail and organizational skills, • Effective written and verbal communication skills