**QC Analyst** Quality Control Albany, NY, US Pay Rate Low: 25.00 | Pay Rate High: 25.00 + Added - 27/06/2025 Apply for Job **Quality Control Analyst** Astrix is proud to partner with a globally recognized contract research, development, and manufacturing organization (CDMO) serving the pharmaceutical and biotech industries. We are seeking a motivated and detail-oriented **Quality Control (QC) Analyst** to join the team. If you're passionate about laboratory science, quality assurance, and contributing to life-saving innovations, this is your chance to work in a high-impact environment with room to grow. **Pay** : 25/hr. **Schedule** : 6pm-6am, Monday-Friday **Key Responsibilities:** + Perform analytical testing on raw materials, in-process and final products, and stability samples using balances, pipettes, pH meters, UV/Vis spectrophotometers, TOC analyzers, and more. + Conduct chromatography (HPLC, GC) testing following comprehensive training and qualification. + Execute wet chemistry assays and routine water sample collections. + Maintain and calibrate QC analytical instruments and general lab equipment. + Support QC laboratory housekeeping and audit readiness efforts. + Assist in reviewing QC data and summarizing findings for management. + Participate in deviation investigations, CAPAs, and out-of-specification (OOS) documentation under guidance from QC Management. + Serve as backup for sample receipt, shipment, result distribution, and external lab coordination. **Qualifications:** **Required:** + Bachelor’s degree in Chemistry or a related scientific field. + 0–3 years of experience in a pharmaceutical QC or analytical laboratory role (entry-level candidates encouraged to apply). **Preferred:** + Experience working in a cGMP, GLP, or FDA-regulated environment. **Key Competencies & Skills:** + Strong understanding of analytical chemistry principles and lab techniques. + Excellent written and verbal communication skills. + Ability to manage time effectively and work independently in a fast-paced environment. + Proficiency with Microsoft Office and laboratory data systems. + Working knowledge of FDA regulations (21 CFR 211, 820, 600) and ISO standards (9001, 13485) is a plus. + Familiarity with statistical analysis, report writing, and documentation best practices. **Physical Requirements:** + Must be able to sit, stand, walk, kneel, or crouch for extended periods. + Ability to lift up to 50 lbs as needed. + Requires fine motor skills, visual focus, and manual dexterity for laboratory work. **Why Join Us?** + Be part of a company with a national and global impact in pharmaceutical development. + Gain valuable experience in an FDA-regulated environment with career advancement opportunities. + Work alongside a collaborative team that values innovation, quality, and continuous learning. _This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!_ \#LIDNPINDBH We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.