Quality Control Technician
AbbVie Inc. - Branchburg, NJ, United States
Posted Jun 10, 2026
Benefits
- Parental leave
- 12 weeks Verified - employer source source checked May 7, 2026
- Non-birth-parent leave
- 12 weeks Verified - employer source source checked May 7, 2026
- Family-building benefits
-
- Fertility benefits: Not verified
- Adoption assistance: Not verified
- Surrogacy assistance: Not verified
- Mental health support
- Not verified
- Relocation assistance
- Not verified
- Childcare support
- Not verified
- Learning budget
- Not verified
- Verification
- Source-linked checked May 7, 2026
- Salary
- Not verified
- 401(k) match
- Reported from DOL Form 5500 industry filing (not employer-specific)
Was this benefit information wrong? Tell us.
Market context
- U.S. role benchmark (BLS OEWS)
- $116,543 U.S. median for this role
- Projected growth (BLS Employment Projections)
- +9.8% - Much faster than average
Matched to SOC 15-1252 - Software Engineering aggregate by role bucket.
Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.
Schedule
- Shift type
- Not verified
- Weekend work
- Not verified
Company
- Equity
- Offered Verified - SEC 10-K source
Application
- Cover letter
- Not verified
- Assessment
- Not verified
- Deadline
- Not stated
Where they hire
State eligibility is not yet verified.
About this role
Quality Control Technician Branchburg, NJ, United States 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: 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. 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
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