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TransMedics

Ex-vivo organ perfusion platform

Quality Calibration Technician

Manufacturing Quality & TestPosted on Nov 13
Full-timeAndover, MA, USAIn-person

About the Job

Requirements

  • At least 2 years of experience performing equipment calibration, metrology, preventive maintenance, or equipment management activities.
  • Working knowledge of metrology principles and precision measurement techniques.
  • Experience using calibration management or computerized maintenance management system (CMMS) software.
  • Experience working in a regulated manufacturing environment.
  • Ability to use calibration standards, measurement instruments, and precision test equipment.
  • Ability to perform the physical activities required, including moving equipment and calibration standards weighing up to 30 pounds.
  • Ability to work in laboratory, manufacturing, warehouse, and cleanroom environments.
  • Ability to follow applicable safety and environmental procedures.

Responsibilities

  • Perform in-house calibrations and verification activities on inspection, monitoring, measurement, and test equipment.
  • Execute routine preventive maintenance activities on production, engineering, and facility-related equipment.
  • Troubleshoot basic equipment issues and coordinate repairs with equipment owners, Engineering, Facilities, and external vendors.
  • Ensure equipment remains calibrated and maintained within established frequencies and specifications.
  • Maintain proper equipment identification, calibration status labeling, and traceability.
  • Maintain the electronic calibration and maintenance management system.
  • Create, issue, and maintain equipment asset records, calibration histories, and maintenance documentation.
  • Review, approve, and archive calibration and preventive maintenance records.
  • Record calibration data and results in designated software systems.
  • Generate and distribute calibration schedules, preventive maintenance schedules, and overdue equipment reports.
  • Establish and maintain calibration files and equipment documentation in accordance with quality system requirements.
  • Schedule and coordinate on-site and off-site calibration and maintenance activities with approved vendors.
  • Collaborate with equipment owners, Facilities, Manufacturing, Engineering, and Quality personnel to minimize operational disruption.
  • Monitor vendor performance and confirm timely completion of calibration and maintenance activities.
  • Ensure compliance with FDA, ISO 13485, and internal quality system requirements.
  • Investigate out-of-tolerance calibration events and support root cause investigations and corrective actions.
  • Assist with equipment qualification, validation, and change control activities as required.
  • Support internal audits, external audits, and regulatory inspections involving equipment management records.
  • Maintain data integrity and documentation accuracy in accordance with Good Documentation Practices.
  • Identify opportunities to improve calibration processes, preventive maintenance programs, and equipment reliability.
  • Participate in equipment lifecycle management initiatives and calibration program optimization efforts.
  • Support implementation and continuous improvement of electronic calibration management systems.
  • Perform other duties and projects as assigned.

Desired Qualifications

  • At least 3 years of experience in the medical device, biotechnology, pharmaceutical, or another FDA-regulated industry.
  • Knowledge of FDA 21 CFR Part 820, Part 211, and ISO 13485 requirements.
  • Experience investigating and documenting out-of-tolerance calibration events.
  • Familiarity with controlled environments, cleanroom operations, and electrostatic discharge (ESD) controls.
  • Experience supporting equipment qualification and validation activities.
  • Strong proficiency with Microsoft Office Suite and electronic quality management systems.
  • Understanding of basic statistical concepts, including averages, standard deviation, and measurement uncertainty.

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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