Quality Control PChem Analyst I or II

Description Join Our Team We are seeking a detail-oriented and motivated Quality Control P-Chem Analyst I or II to join our Quality Control team. In this role, you will support the analysis of bioanalytical and production samples while helping ensure the quality, safety, and integrity of our products. If you enjoy working in a collaborative laboratory environment focused on scientific excellence and continuous improvement, we'd love to hear from you. Benefits include: Up to 4 weeks of paid vacation Paid holidays Medical, dental, vision, and prescription insurance for employees and eligible dependents 401(k) retirement plan with employer match Opportunities for professional growth and continued learning Requirements Position Summary The Quality Control P-Chem Analyst I/II performs analytical testing on bioanalytical and production samples received from contract research organizations, manufacturing operations, and research and development. This position supports quality assurance efforts by following current Good Manufacturing Practices (cGMP), Good Laboratory Practices (cGLP), established Standard Operating Procedures (SOPs), and validated test methods. Essential Responsibilities Perform analytical testing of bioanalytical specimens, including blood, urine, and tissue samples. Analyze production and research samples using laboratory instrumentation and analytical techniques. Operate, maintain, calibrate, and troubleshoot laboratory equipment and analytical instruments. Follow all Standard Operating Procedures (SOPs), Test Methods (TSMs), cGMP, cGLP, and internal quality processes. Assist with laboratory equipment qualification, validation, and calibration activities. Prepare, revise, and maintain test methods, SOPs, and other quality documentation. Review analytical data for accuracy and completeness. Identify and communicate issues that could affect product identity, strength, quality, purity, compliance, or laboratory efficiency. Support Research & Development projects and laboratory investigations. Maintain laboratory inventory, Safety Data Sheets (SDS), and assist with purchasing laboratory supplies. Complete all required training and maintain training records. Participate in continuous improvement initiatives. Perform other duties as assigned. Qualifications Education Bachelor's degree in Chemistry, Biology, Biochemistry, Pharmaceutical Sciences, or another related scientific discipline preferred. Equivalent combinations of education and relevant laboratory experience will be considered. Experience Quality Control Analyst I One (1) year of laboratory experience. Quality Control Analyst II Two (2) to three (3) or more years of progressively responsible laboratory experience, preferably in a regulated pharmaceutical, biotechnology, or medical device environment. Knowledge, Skills & Abilities The ideal candidate will have: Working knowledge of cGMP and cGLP requirements Strong analytical and problem-solving skills Experience operating analytical laboratory instrumentation Excellent attention to detail and organizational skills Strong written and verbal communication skills Proficiency with Microsoft Office applications Ability to work independently while collaborating effectively with a team Ability to read, interpret, and follow technical documents, SOPs, and laboratory procedures Commitment to safety, quality, accuracy, and continuous improvement Physical Requirements Ability to occasionally lift up to 20 pounds Ability to work safely in a laboratory environment Reasonable accommodations will be made to enable qualified individuals with disabilities to perform the essential functions of the position Compensation $25.00-$28.00 per hour , based on qualifications and experience. Schedule Day or Night Shift Opportunities Available #J-18808-Ljbffr Socket.dev