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TransMedics

Ex-vivo organ perfusion platform

Test Engineer

Validation, Compliance & Quality SystemsConfirmed live in the last 24 hours
Full-timeAndover, MA, USANo salary listed

About the Job

Requirements

  • A Bachelor of Science degree in Engineering and four years of experience working in an FDA- or ISO-regulated medical device or medical equipment industry, or an equivalent combination of education and experience.

Responsibilities

  • Develop hardware and software solutions for PCBA-level and system-level functional tests, including LabView PCBA testing, leak and flow testing, electrical testing, and system functional testing.
  • Work with Design and Manufacturing Engineering to develop test parameters and requirements that evaluate all design requirements and minimize or remove gaps in test coverage.
  • Write and perform validation activities for new and existing production tests related to implementing and validating production test equipment and fixtures.
  • Create, implement, and maintain test software in the LabView environment for existing and new programs.
  • Implement and maintain existing and new leak and flow test equipment.
  • Create, revise, release, and maintain test procedures through controlled document change order procedures.
  • Transition board-level functional tests to contract assembly suppliers where applicable.
  • Support Engineering and Production team efforts to identify opportunities to streamline production through process, test, and product design changes.
  • Support Technical Service activities, including OCS system troubleshooting and upgrades.
  • Work with Quality Assurance to maintain an approved internal Quality System that meets cGMP, QSR, and ISO requirements.
  • Provide training in testing, troubleshooting, and inspection methods as required.
  • Perform other TransMedics tasks and duties as required.

Desired Qualifications

  • Proven experience fabricating and validating test equipment and procedures for electro-mechanical and functional test equipment in an FDA- or ISO-regulated medical device or medical equipment industry.
  • Expertise in electronic testing, troubleshooting, and repair of printed circuit boards.
  • Experience with IPC standards, including J-STD-001 soldering of electrical and electronic components, IPC-A-610/620 PCB and wire harness inspection, and IPC-7711/7721 rework and repair of electronic assemblies; formal training or certification is a plus.
  • Knowledge of LabView programming; formal training is a plus.
  • Formal Six Sigma training is a plus.

About the Company

TransMedics

Ex-vivo organ perfusion platform

TransMedics develops the Organ Care System (OCS), a portable device that keeps donor organs alive outside the body using warm, oxygenated perfusion, allowing continuous viability monitoring and assessment. It makes money by selling the OCS consoles, selling disposable sets per transplant, and offering the National OCS Program, which provides trained procurement surgeons, clinical support, and dedicated organ transport logistics. The company stands apart by having FDA-approved preservation and assessment for hearts, lungs, and livers, including DBD and DCD indications, and by offering an integrated hardware, disposables, and logistics platform. Its goal is to increase viable transplants and donor organ utilization by improving preservation, assessment, and logistics across transplant centers.

Company size
501-1,000
Company stage
IPO
Headquarters
Andover, MA
Founded
1998

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