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AbbVie

Global biopharmaceutical company developing medicines

Laboratory Technician

Regulatory & Quality (Life Sciences)Posted on Nov 10
Full-timeBranchburg, NJ, USAIn-person

About the Job

Requirements

  • A bachelor's degree in a related science, such as Biology, Chemistry, or Biochemistry, is required.
  • 1–4 years of experience performing duties in a Good Manufacturing Practice environment, specifically in an aseptic processing facility.
  • Experience in a cleanroom setting is required.
  • Experience with routine laboratory testing and/or environmental monitoring.
  • Experience with standard laboratory equipment such as pH meters and particle monitors.
  • Ability to lift 25 pounds and wear proper personal protective equipment.

Responsibilities

  • Perform, document, and report Quality Control Laboratory testing, including packaging seal strength tests, water testing, cleanroom environmental monitoring, data entry and verification, growth promotion tests, and other required laboratory testing.
  • Perform environmental monitoring of aseptic manufacturing operations, including non-viable and viable air particulate sampling, viable surface sampling, personnel monitoring, and water sampling.
  • Conduct on-the-spot investigations and appropriate follow-up actions under environmental monitoring excursion situations, under the direction of senior technicians or management and according to procedure.
  • Complete Environmental Monitoring Requests in a timely manner to release cleanrooms to Manufacturing according to procedure.
  • Complete personnel monitoring plating of Manufacturing technicians as requested.
  • Sample and test water systems serving the manufacturing facility and laboratories.
  • Follow standard operating procedures to perform Quality Control Laboratory testing.
  • Operate standard laboratory equipment, including balances, autoclaves, CLIMETs, Instron units, a thermogravimetric analyzer, and air samplers.
  • Maintain databases and spreadsheets to accurately report test results in compliance with current Good Laboratory Practices and Good Documentation Practices.
  • Perform data verification for environmental monitoring results and data entry, and become a qualified peer reviewer.
  • Ensure records and raw data are properly recorded, reviewed, and retained.
  • Keep supervisors and upper management informed of laboratory operation status.
  • Initiate Laboratory Investigation Records in the Global Trackwise system.
  • Execute non-routine tests for study protocols and/or equipment re-qualifications.
  • Ensure adequate laboratory supplies and proper functioning of equipment.
  • Ensure solutions and media are disposed of according to standard operating procedures.
  • Monitor preventive maintenance and calibration activities of laboratory equipment.
  • Sustain 6S and maintain a safe and pleasant laboratory working environment.

About the Company

AbbVie

Global biopharmaceutical company developing medicines

AbbVie is a global biopharmaceutical company that develops and sells medicines to treat serious health conditions. Its portfolio spans immunology, oncology, virology, neuroscience, and aesthetics, with products designed to modulate the immune system, target disease pathways, or support medical aesthetics. AbbVie compounds its products through a heavy emphasis on research and development, investing billions to build a steady pipeline of new therapies. Its medicines are brought to market by selling to healthcare providers, hospitals, and clinics, and in some cases directly to patients via prescriptions. The company differentiates itself through a wide, globally distributed product line, substantial R&D investment, and a commitment to sustainability and patient care, including science-based targets. AbbVie’s goal is to improve patient outcomes by delivering effective treatments for unmet medical needs while pursuing long-term, responsible growth across healthcare markets.

Company size
10,001+
Company stage
IPO
Headquarters
North Chicago, IL
Founded
1888

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