Technical Writer

AbbottScarborough, ME
Onsite

About The Position

This position works out of our Scarborough, ME location in the Infections Disease, Diagnostics Division. We’re empowering smarter medical and economic decision-making to help transform the way people manage their health at all stages of life. Every day, more than 10 million tests are run on Abbott’s diagnostics instruments, providing lab results for millions of people. The Technical Writer will provide guidance & support to the team in order to produce quality products, seek continuous improvement, and achieve established goals and targets for safety, quality, and productivity.

Requirements

  • Bachelor’s Degree or equivalent combination of education and experience.
  • 2+ years’ experience in a manufacturing environment.
  • Prior experience utilizing GMP practices/techniques.

Nice To Haves

  • Comprehensive understanding of operational excellence/lean principles and applications.
  • Comprehensive understanding of medical device manufacturing.

Responsibilities

  • Complete Quality Incident (QI) and CAPA Investigations to support Production.
  • Collaborate with QI Coordinators and Approvers and the Material Review Board to receive timely approval of QIs in support of the manufacturing plan.
  • Work closely with the Production Manager and Supervisors to ensure all production objectives are met or exceeded.
  • Adjust priorities quickly.
  • Write and execute reprocessing/rework records independently or with QA assistance.
  • Create and move material quarantine records and disposal records independently.
  • Develop and implement corrective actions to improve product and process conformance.
  • Complete Change Orders to update Production SOPs.

Benefits

  • Free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
  • An excellent retirement savings plan with a high employer contribution.
  • Tuition reimbursement
  • the Freedom 2 Save student debt program
  • FreeU education benefit
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