

New · posted Nov 15
TransMedics · Medical Devices
Quality Calibration Technician
- Andover, MA
- On-site
- Full-time
- Associate & Specialist
The role
The Equipment Quality & Controls Technician is responsible for the hands-on calibration, maintenance, control, and compliance of inspection, test, and manufacturing equipment used throughout TransMedics' operations. This role ensures equipment remains within established specifications and regulatory requirements through the execution of calibration activities, preventive maintenance, equipment troubleshooting, vendor coordination, and documentation management.
The ideal candidate possesses strong knowledge, experience with calibration systems, and a solid understanding of FDA-regulated manufacturing environments. This position works closely with Manufacturing, Engineering, Facilities, and external service providers to maintain a compliant and effective Equipment Quality & Controls management program.
What you need
Minimum Qualifications
- 2+ years of experience performing equipment calibration, metrology, preventative maintenance, or equipment management activities.
- Working knowledge of metrology principles and precision measurement techniques.
- Experience using calibration management or CMMS software systems.
- Experience working in a regulated manufacturing environment.
Knowledge, Skills & Abilities
- Strong hands-on mechanical and technical aptitude.
- Ability to use calibration standards, measurement instruments, and precision test equipment.
- Strong analytical and troubleshooting skills.
- Excellent organizational skills with the ability to manage multiple priorities simultaneously.
- Strong verbal and written communication skills.
- Ability to work independently and collaborate effectively within cross-functional teams.
- Detail-oriented with a commitment to quality, compliance, and data integrity.
Physical Requirements
- Ability to sit, stand, walk, bend, squat, kneel, reach, and lift equipment as required.
- Ability to safely move equipment and calibration standards weighing up to 30 pounds.
- Fine motor skills necessary to operate measurement devices, hand tools, and computer systems.
- Ability to work in laboratory, manufacturing, warehouse, and cleanroom environments.
- Ability to distinguish colors, read instrument displays, and interpret technical documentation.
- Ability to follow all applicable safety and environmental procedures.
TransMedics, Inc. is a commercial-stage medical technology company transforming organ transplant therapy for patients worldwide. Our mission is to help save more patients’ lives by increasing access to viable donor organs for those who are awaiting an organ transplant. To accomplish this mission, we partner closely with transplant stakeholders worldwide and help expand their access to healthy donor organs, while delivering the highest quality technology, service, clinical care and outcomes.
Driven by a passion for improving patient care, we make the impossible possible and keep our employees at the center of everything we do. Together, we strive to enhance the quality of life for transplant recipients and their families, fostering hope and healing in the journey toward better health.
Maximize your potential at TransMedics, Inc.
TransMedics is committed to equitable and transparent compensation. The expected hourly rate for this role is $35.00 - $42.00 which represents the company’s current good-faith estimate of compensation for this position. Actual hour rate will depend on factors such as, but not limited to, candidate experience, qualifications, skills, and the specific work location. Hourly roles may also be eligible for overtime, shift differentials, incentive programs, and our comprehensive benefits package (medical, dental, vision, retirement savings, paid time off, and wellness resources). We comply with all U.S. pay transparency laws and do not request or consider salary history.
Preferred Qualificationsnice to have
- 3+ years of experience in the medical device, biotechnology, pharmaceutical, or other FDA-regulated industry.
- Knowledge of FDA 21 CFR Part 820, Part 211, and ISO 13485 requirements.
- Experience investigating and documenting Out-of-Tolerance (OOT) calibration events.
- Familiarity with controlled environments, cleanroom operations, and 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.
What you'll do
Equipment Calibration & Maintenance
- Perform in-house calibrations and verification activities on inspection, monitoring, measurement, and test equipment.
- Execute routine preventative 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.
Calibration Program Administration
- 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 preventative maintenance records.
- Record calibration data and results in designated software systems.
- Generate and distribute calibration schedules, PM schedules, and overdue equipment reports.
- Establish and maintain calibration files and equipment documentation in accordance with quality system requirements.
Vendor & Cross-Functional Coordination
- 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 ensure minimal disruption to operations.
- Monitor vendor performance and confirm timely completion of calibration and maintenance activities.
Compliance & Quality Support
- Ensure compliance with FDA, ISO 13485, and internal quality system requirements.
- Investigate out-of-tolerance (OOT) 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 (GDP).
Continuous Improvement
- 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.
Pay
$72,800 – $87,360 a year
Employer provided$35.00 – $42.00 an hour · yearly at 2,080 hours (40 a week)
How this comparesMedical with Health Reimbursement Account through Blue Cross/Blue Shield of MA
Dental
Vision
Healthcare Flexible Spending Account
Dependent Care Flexible Spending Account
Short Term Disability
Long Term Disability
401K Plan
Pet insurance
Employee Stock Purchase Plan
Where you'll work
Andover, MAOn-siteOpen in Maps (opens in a new tab)
More jobs in Andover, MAEqual opportunity, accessibility and legal noticesTransMedics's statements, word for word
TransMedics is an equal opportunity employer and does not discriminate on the basis of race, color, religion, sex, national origin, marital status, age, disability or protected veteran status, or any other characteristic protected by law. We are committed to creating an inclusive environment for all employees.
Job intelligence
The context around this role
Live data · November 15, 2026
Salary intelligence
How the pay compares
This role's midpoint is 3% below the US median for Quality Engineering roles at this level.
This roleEmployer provided
Associate & Specialist roles in Massachusetts5 roles publishing pay
Associate & Specialist roles in the US50 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $72,800 | — | $87,360 |
| Massachusetts (middle half) | $78,500 | $80,000 | $80,000 |
| All US (middle half) | $73,000 | $82,250 | $99,000 |
This role: TransMedics's own published range, converted to a year at 2,080 hours. Comparisons: the base pay employers published on open Quality Engineering roles at the same level on Regulatory Jobs, November 15, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Engineering
The general path across 214 open Quality Engineering roles on Regulatory Jobs, with the titles they carry most. Not TransMedics's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 54 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Documentation and SOPs11
- GMP and compliance6
- Lab testing and methods6
- Quality systems and risk6
- Data and digital systems6
- Collaboration and leadership4
- Investigations and CAPA3
- Validation and qualification2
- Regulatory submissions1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Quality Engineering work in medical devices, led by the three this posting names, each linked to the agency or standards body that publishes it.
- FDA21 CFR Part 820 (QMSR)(official source, opens in a new tab)FDA quality management system regulation for medical devices, aligned with ISO 13485Named in the posting
- ISOISO 13485(official source, opens in a new tab)Quality management systems for medical devicesNamed in the posting
- FDAFDA data integrity guidance(official source, opens in a new tab)Data Integrity and Compliance With Drug CGMP: Questions and AnswersNamed in the posting
- ISOISO 14971(official source, opens in a new tab)Application of risk management to medical devices
- ISOISO 2859-1(official source, opens in a new tab)Sampling procedures for inspection by attributes (AQL sampling plans)
- EUEU MDR (Regulation 2017/745)(official source, opens in a new tab)The EU Medical Device Regulation: CE marking, technical documentation, vigilance
- FDAFDA Investigations Operations Manual(official source, opens in a new tab)How FDA investigators plan and conduct inspections
- ISOISO 14644-1(official source, opens in a new tab)Cleanroom air cleanliness classification by particle concentration
- ISOISO/IEC 17025(official source, opens in a new tab)Competence of testing and calibration laboratories
- ISOISO 19011(official source, opens in a new tab)Guidelines for auditing management systems
- IECIEC 62366-1(official source, opens in a new tab)Application of usability engineering to medical devices
- ISOISO 10993-1(official source, opens in a new tab)Biological evaluation of medical devices within a risk management process
- ISOISO 11135(official source, opens in a new tab)Ethylene oxide sterilization of health care products
- ISOISO 11137-1(official source, opens in a new tab)Radiation sterilization of health care products
- ISOISO 11607-1(official source, opens in a new tab)Packaging for terminally sterilized medical devices
- ISOISO 11737-1(official source, opens in a new tab)Determination of the microbial population (bioburden) on medical devices
Company hiring pulse
TransMedics on Regulatory Jobs
- 12
- Open roles
- 12
- Distinct roles
- 1
- Locations
By discipline
- Quality10 83%
- Regulatory1 8%
- Clinical1 8%
By level
- Senior & Principal5 42%
- Associate & Specialist5 42%
- Manager2 17%
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Quality Calibration Technician at TransMedics
Open until filled. $73K–$87K a year, employer provided.


