Quality Control Technician

Responsibilities

• Responsible to enter test results in manufacturing systems such SAP, POMS, and LIMS.
• Interprets experimental data for conformance with product and material specifications.
• Perform in-process laboratory tests such as Karl Fischer and Torque removal testing, as written per procedure
• Responsible for correct documentation and compliance with GDP requirements of the tasks performed.
• Performs visual inspection of finished and in-process materials, classifies defects, and determines test disposition
• Performs test methods as written to support product/material release.
• Reviews and verifies manufacturing operating settings.
• Makes suggestions for improvement based upon scientific and good manufacturing practices understanding.
• Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements.
• Accepts responsibility for acquiring knowledge and experience to support continual personal development.
• Budget time effectively to carry out assigned tasks and takes initiative to be involved in team activities and decision making.
• Works with others to maintain a positive atmosphere to accomplish business objectives and is an active participant in the work structure and fosters positive working relationships with all levels of the organization
• High School Diploma required
• Technical Degree preferred.
• 1 to 2 years of experience conducting quality inspections in a pharmaceutical setting is required.
• 1-2 years of experience working in a laboratory setting is preferred.
• Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
• 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 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

Benefits

Additional Information

Performs functions associated with cGMP manufacturing operations within the drug product manufacturing and packaging facility, including performing visual inspection of both finished and in-process materials, verifying manufacturing data in the batch record system, and conducting testing on in-process materials. Uses sophisticated programs (such as POMS and SAP) to evaluate operating data, which can be used to determine acceptable quality limits and product release requirements.

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