Quality Control Technician

Quality Control TechnicianThe Quality Control Technician performs final inspection of finished goods in accordance with established procedures, documents inspection results in the applicable quality system, and supports product release activities. This role is part of a dynamic team that interfaces closely with the product release and packaging departments to help ensure seamless product flow and timely delivery. The Quality Control Technician also contributes to problem-solving efforts, including nonconformance investigations, rework, and continuous improvement initiatives.ResponsibilitiesPerform final inspection of products in accordance with established procedures, including visual inspections and final packaging checks, to ensure labeling, packaging, inserts, and other components conform to applicable quality standards and product specifications.Accurately document final product inspection results in the applicable quality system to determine product acceptability for use or transfer to the next stage of release.Notify management of any nonconformance to product specifications and support related investigations. Ensure item or product disposition is conducted in accordance with established nonconformance and quality procedures.Properly segregate, store, and quarantine finished goods in designated quality hold areas, ensuring all items are accurately labeled to reflect their status.Document, execute, and track rework activities for nonconforming products, ensuring all associated records are complete, accurate, and maintained in accordance with established procedures and quality requirements.Support management with cross-functional projects, reporting, and performance metrics as needed to drive operational effectiveness and continuous improvement.Attend and actively participate in meetings, contribute insights, escalating issues appropriately, and supporting timely resolution of operational priorities.Maintain safety first culture by consistently following established safety practices and actively seek opportunities to improve safety.QualificationsMinimum High School graduate; Bachelor's or Associate's degree desired2+ years of overall experience in Manufacturing, Quality or EngineeringKnowledge of GMP regulations and standards affecting pharmaceutical productsGood verbal and written communication skillsDemonstrated analytical skills and attention to detailGood interpersonal relations/communications skillsMust be available to work daily overtime, including weekends, as neededPreferred1+ years experience in inspections of GMP manufactured products with in the pharmaceutical or medical device industry is highly desired5 years experience in a Manufacturing and/or Finishing and/or Packaging environment2 years experience in Batch Record ReleaseAdditional InformationThe compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.This job is eligible to participate in our short-term incentive programs.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 & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: Fraud AlertAbbVie will never request sensitive personal information (such as bank account details, social security numbers, or payment of any kind) during the recruitment process.If you suspect you have received a fraudulent offer or communication claiming to be from AbbVie, please do not respond, open any attachments, or click on any hyperlinks.If you have any questions or concerns regarding the authenticity of a communication alleged to have been made by or on behalf of AbbVie, please contact us immediately.Protect yourself by verifying job offers and communications. Your safety is important to us.Pay Range: $26.2 - 47.3 USDWhere We WorkRole is exclusively performed at a site or office and onsite presence is required. Employees who are site/office-based and can occasionally perform their role virtually work both in the office and remotely*, following the policies and regulations in place at their location. US Employees must be in the office on Tuesday, Wednesday, and Thursday with flexibility to work remotely on Mondays and Fridays. Three days in the office is the minimum; some individuals or teams may require more in-office days due to meetings, business/project needs or their role.