Senior Technician, Stability - North Chicago Illinois

Company: AbbVie
Location: North Chicago, Illinois
Posted On: 03/20/2026

Company Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description The Senior QC Technician is responsible for the timely and accurate management of retain, stability, and reference standard samples in compliance with established policies and procedures for multiple global AbbVie sites and third-party partners. This role demonstrates proficiency in operating multiple systems to execute activities such as receipt, storage, inspection, dispensing, and shipping with minimal error. The Senior QC Technician actively implements new technologies and processes, assumes ownership of assigned tasks and objectives, and independently prioritizes their work schedule to ensure all goals are met. Responsibilities Independently works in multiple systems as assigned and can effectively perform a multitude of tasks for which they are trained on with minimal error, while adjusting to unforeseen obstacles to accomplish assignments. Budgets their time effectively to carry out assigned tasks and makes recommendations for improvement. Takes initiative to be involved in team activities and decision making. Accepts responsibility to complete assigned tasks as committed and proactively identifies and performs new tasks outside area of responsibility. Maintain stability chambers, dispensing laboratory, and samples in an orderly audit-ready state Receive, store, inspect, dispense, ship and purge samples according to procedures. Maintain accurate and thorough documentation. Communicate with multiple functional groups. Responsible for compliance with cGMP guidelines, DEA controlled substance regulations and maintenance of training requirements. Responsible for compliance with applicable shipping requirements and record retention for international, domestic, dangerous goods, Occupational Safety and Health Administration, and Corporate and Functional policies. These responsibilities will sometimes require walking over one mile per day and will routinely require standing in place for prolonged periods of 2 hours or more per day. Lifting heavy objects up to 50 lbs. will be required when occasionally handling large shipments of samples. In addition, handling of hazardous materials will be required with proper use of personal protective equipment. Qualifications Bachelors degree, with 2 years experience in a government regulated pharmaceutical industry, or a high school diploma with 5 years of experience in government regulated pharmaceutical industry. General knowledge of cGMP for documentation and laboratory practices. Strong attention to detail and organizational skills. Good interpersonal relations skills, verbal and written communication skills. Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law: The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at the timeofthis posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographic location,andwemay ultimatelypay more or less than the posted range. This range may be modified in thefuture. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees. This job is eligible to participate in our short-term incentiveprograms. Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.The amount and availability of anybonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employee remains in the Company's soleandabsolutediscretion unless and until paid andmay be modified at the Companys sole and absolute discretion, consistent withapplicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html More...

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