Becton Dickinson Medical Devices-posted 2 days ago
Full-time • Mid Level
Onsite • Sparks, NV
5,001-10,000 employees

We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you’ll be supported to learn, grow and become your best self. Become a maker of possible with us. Summary The ID/AST (Phoenix) QC Specialist II is a laboratory scientist, whose primary responsibility will be split between processing data generated from Quality Control testing of Phoenix disposable products and complaint investigations. The position will also be responsible for supporting the Phoenix Quality Control Lab by, but not limited to QC testing of Phoenix disposable products and all lab-related duties.

  • Upload and archive Phoenix instrument data.
  • Print Resident Panel Reports.
  • Copy, process, and import instrument data via queries.
  • Print reports, review data and analyze results for trends.
  • Completion of Phoenix Quality Control laboratory testing documentation and evaluation of test results against specifications to make pass / fail determinations.
  • Communicating results to the appropriate Plant personnel.
  • Generation of Quality Notifications upon testing failures.
  • Work closely with Product Support to evaluate and recommend proactive solutions.
  • Archive processed data and updating the MRB Database.
  • Review and release of drugs and substrates (frozen stocks) for the Solution Preparation department.
  • Perform routine Phoenix Quality Control testing, as well as any additional lab-related duties or special projects.
  • Coordination of complaint investigations including adhering to turnaround times and presenting findings during complaint meetings.
  • Additional duties and responsibilities as determined.
  • Able to handle a fast paced work environment
  • Able to adapt to rapid changes in prioritization
  • Able to take feedback and direction from the plant level Quality Engineers
  • Bachelor Degree in Biology/Microbiology or other related Life Science.
  • 3 years of relevant experience.
  • Knowledge of IVD industry regulations (FDA, GMP/QSR, ISO, CE).
  • Knowledge of spreadsheet, word processing, and database applications.
  • Good verbal and written communication skills.
  • Team oriented.
  • Must demonstrate the ability to solve problems and make independent sound decisions.
  • ASQ Certification, Medical Laboratory Technician, or Medical Technologist Certification a plus.
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