2nd Shift Quality Chemist (Relo Offered)

Job Description The Quality Chemist supports the quality laboratory by performing release, stability, and special request testing on finished products and raw materials in a safe and compliant environment. This role requires strong time management skills, the ability to independently execute laboratory methods and procedures, and a willingness to learn laboratory processes, instrumentation theory, and troubleshooting. The Quality Chemist works closely with laboratory management and teammates to ensure accurate, timely testing and adherence to regulatory and internal quality standards. Responsibilities Perform release, stability, and special request testing of finished products and raw material samples in accordance with SOPs, in‑house test methods, and compendial methods. Independently execute in‑house methods and procedures as written with minimal assistance, ensuring accuracy and compliance. Adapt to changes in the testing schedule and support laboratory improvements implemented by management and team members. Assist with training new laboratory personnel and document training activities in accordance with laboratory SOPs and the company training program. Maintain a strong safety‑first mindset, remaining aware of surroundings and following all laboratory safety practices. Ensure all equipment used in testing procedures is calibrated, properly maintained, and used according to established procedures. Train on the operation of laboratory instrumentation including, but not limited to, laboratory balances, HPLC, GC, automated titrators, FTIR, UV/Vis spectrophotometers, polarimeters, dissolution and disintegration instrumentation. Learn and operate additional instrumentation and new laboratory test methods as required. Execute projects assigned by management within established deadlines while effectively managing time and testing responsibilities. Stay current on publications and requirements from USP, FDA, and other relevant regulatory bodies to help ensure compliance in analytical applications, release specifications, and documentation practices. Maintain competency in ISO test methods and ensure they are current and properly applied. Assist in resolving laboratory Out‑Of‑Specification (OOS) results in accordance with laboratory investigation procedures when assigned. Perform other duties as required to meet company objectives and support overall laboratory operations. Communicate effectively with other departments and collaborate within a team environment to achieve quality and production goals. Demonstrate strong attention to detail and apply process analytical skills to support accurate and reliable testing. Maintain regular and reliable attendance. Perform physical activities required in the laboratory and production environment, including standing and bending regularly, climbing stairs, using hands and arms to lift and reach, standing and walking for a minimum of 8 hours, lifting, pulling, and pushing a minimum of 50 pounds, using both arms to push, pull, or lift, and bending and squatting as needed. Apply basic math skills, including the use of fractions, decimals, and commercial arithmetic, and demonstrate a basic knowledge of grammar, spelling, and punctuation for documentation and reporting. Essential Skills Bachelor of Science degree in Chemistry. 2–5 years of experience working in a cGMP facility. Experience with instrumentation such as HPLC, GC, and LC, including familiarity with the instruments and the ability to troubleshoot issues, ideally with a minimum of 2 years of experience. Proficiency in laboratory analytical techniques such as titrations, gravimetric methods, and sample preparation. Ability to manage time efficiently to complete assigned testing and projects within deadlines. Strong attention to detail and accuracy in performing laboratory tests and documenting results. Ability to read, understand, and follow SOPs, in‑house test methods, and compendial methods. Basic math skills, including the use of fractions, decimals, and commercial arithmetic. Basic knowledge of grammar, spelling, and punctuation for clear and accurate documentation. Commitment to working safely in a laboratory environment and maintaining a safety‑first mindset. Additional Skills & Qualifications Experience using Empower software is preferred but not required. Experience working with ISO test methods and maintaining current competency is beneficial. Ability to learn and apply instrumentation theory and troubleshooting techniques for a range of analytical equipment. Strong verbal and written communication skills to effectively collaborate with cross‑functional teams. Demonstrated flexibility in adapting to changing testing schedules and laboratory process improvements. Ability to assist in laboratory investigations, including Out‑Of‑Specification (OOS) result resolution, following established procedures. Alignment with core values such as honesty, integrity, commitment, and responsibility. Motivation to stay current with USP, FDA, and other relevant regulatory guidance related to analytical testing and documentation. Willingness to take on additional projects and duties to support laboratory and company objectives. Work Environment This role is based in a quality control laboratory environment that emphasizes safety, regulatory compliance, and collaboration. The position operates on an afternoon and evening shift schedule, with hours from Monday through Thursday, 3:30 p.m. to 11:30 p.m., and Friday, 1:30 p.m. to 9:30 p.m. The quality chemist works with a wide range of analytical instrumentation, including laboratory balances, HPLC, GC, LC, automated titrators, FTIR, UV/Vis spectrophotometers, polarimeters, and dissolution and disintegration instruments. The work involves standing and walking for extended periods, regularly bending and squatting, climbing stairs, and using both arms to lift, push, and pull up to 50 pounds. The environment requires strict adherence to laboratory safety practices, SOPs, and cGMP standards, as well as accurate documentation and communication. The organization offers a performance‑based culture with discretionary bonus potential worth up to 12% of year‑to‑date earnings, pro-rated in the first year, and places a strong emphasis on values such as honesty, integrity, commitment, and responsibility. Job Type & Location Permanent position based out of Lancaster, SC. Pay And Benefits Salary: $70,000.00 – $75,000.00 per year. Featured benefits : Medical insurance, Vision insurance, Dental insurance, 401(k), Disability insurance, Tuition assistance, Child care support. Workplace Type Fully onsite position in Lancaster, SC. Application Deadline This position is anticipated to close on Jul 16, 2026. Equal Employment Opportunity Statement The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. #J-18808-Ljbffr Actalent