QC Analyst I- 3rd Shift Weekends (7 pm-7:30 am)

Position Summary The QC Analyst I position is responsible for all daily laboratory testing of raw materials, in-process and finished products. In addition, this position provides support for routine laboratory tasks and analysis, including but not limited to environmental monitoring, equipment calibrations/ verifications, raw material sampling, laboratory/production process testing including chromatography analysis. Essential Functions Perform chemical testing using analytical instrumentation and wet bench techniques including pH, viscometers, FTIR, UV-VIS, TOC, gas chromatography, and liquid chromatography. Perform minor troubleshooting of testing and instrumentation as necessary and write minor laboratory investigations. Assist in completing all laboratory investigations, including out of specification investigations, as required by management. Sample raw materials for QC lab testing, as well as perform the required testing for raw material release. Sample and perform analysis for site environmental monitoring. Perform routine maintenance, calibrations, and verifications of QC laboratory equipment. Be familiar with quality GMP documentation of testing results and assurance of laboratory data integrity. Maintain accurate lab notebooks and complete all related analytical reports, write summaries, and keep proper documentation in compliance with SOPs. Have experience with USP interpretation and testing. Support QC audit readiness with understanding of FDA and ISO regulations and requirements. Support on-time performance in the QC lab against the production and laboratory schedules. Maintain a safe, clean, and organized environment for all QC areas. Employ sound and compliant laboratory techniques and logic per industry standards (e.g., FDA, USP/NF, ISO, ANSI) and internal and customer requirements. Review QC lab testing and processes for adherence to lab and site SOPs. Follow all SOPs and safety guidelines to ensure compliance with a cGMP environment and safety practices. Perform any additional functions as assigned by the laboratory manager. Education Associate’s degree with 5+ years of laboratory experience (chromatography experience preferred). Bachelor’s degree in chemistry or related field with 1–2 years of experience. Experience Knowledge of analytical instrumentation (pH, viscosity, FTIR, UV-VIS, etc.). Experience working in an ISO or FDA-regulated environment preferred. Proficiency with Microsoft Office and other software. Excellent communication skills, including the ability to speak clearly, listen and gain clarification, respond well to questions, and write clearly and informatively. Skills & Abilities Computer skills and literacy. Experience with Microsoft Office, LIMS, Empower, and other software. Laboratory skills: wet bench testing, standard preparation, balance use/weighing, microbiology techniques. Work Environment Ventilated, well‑lighted laboratory with work benches, vented hoods, and tile or epoxy flooring. Temperature controlled. Benefits Medical, dental, and vision insurance. Company paid short‑term disability, long‑term disability, and AD&D. Annual anniversary cash award. Quarterly perfect attendance bonus. On‑site nurse. Company paid employee assistance plan. 401(k) with match. And much more. Ortec is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sexual orientation, gender identity, national origin, veteran or disability status. #J-18808-Ljbffr