A2 Shift: 6pm-6:30am Sunday/Monday/Tuesday & every other Saturday (15% Differential)This role supports cGMP manufacturing operations within the biologics production facility, working with engineers on set‑up, calibration, rework, and quality testing of parts, components, and final materials. The position uses programs such as LIMS, SAP, and automated control systems to collect and evaluate operating data and may assist in developing methods and procedures to control or modify the manufacturing process.ResponsibilitiesShipping finished materials.Maintaining inventory levels.Sampling of in‑process and raw materials.Operating glass washer / autoclave.Buffer/media preparation.Equipment preparation (CIP / SIP).Cell culture (from vial thaw to production scale).Column chromatography.Tangential flow filtration.QualificationsHigh School diploma (or equivalent) with 2+ years experience; Associate's degree in science with 1+ years relevant experience; Bachelor's degree with 0+ years relevant experience.Acquires job skills and learns company policies and procedures to complete routine tasks.Works on routine assignments requiring limited judgment.Recognizes when accepted practices are deviated from.Receives detailed instructions and works under close supervision.Compensation & BenefitsThe compensation range reflects the base pay for this role, which may vary with geography. The company offers a comprehensive benefits package that includes paid time off (vacation, holidays, sick), medical/dental/vision insurance, 401(k) for eligible employees, and short‑term incentive programs.AbbVie is an equal‑opportunity employer committed to integrity, innovation, and service to our community. All qualified applicants, including veterans and people with disabilities, are encouraged to apply.#J-18808-Ljbffr