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TransMedics

Ex-vivo organ perfusion platform

Senior Software Quality Engineer

Regulatory & Quality (Life Sciences)Posted on Nov 13
Full-timeAndover, MA, USAIn-person

About the Job

Requirements

  • At least 5 years of experience implementing or supporting enterprise software systems, such as QMS, ERP, PLM, MES, or similar platforms.
  • Strong working knowledge of quality system processes, including CAPA, complaints, audits, and change control, in a regulated environment.
  • Hands-on experience with system configuration, testing, validation, and troubleshooting.
  • Experience with software validation principles (CSV/CSA) and data integrity requirements.
  • Ability to work cross-functionally with technical (IT) and non-technical stakeholders.
  • Ability to diagnose issues and independently drive resolution.
  • Ability to manage multiple priorities and drive work forward in a fast-paced environment.

Responsibilities

  • Lead configuration, setup, and deployment of enterprise software systems supporting Quality and cross-functional processes.
  • Perform independent review and approval of software validation documentation, including plans, protocols, and reports, as the Quality representative, ensuring compliance with regulatory and internal requirements.
  • Partner with IT to support system integrations, data structures, access controls, and technical troubleshooting.
  • Translate business and quality process requirements into system configurations, workflows, and scalable solutions.
  • Lead and execute system validation activities, including IQ/OQ/PQ and UAT, ensuring compliance with applicable regulatory requirements.
  • Troubleshoot system issues, perform root cause analysis, and implement solutions; support data migration, data integrity checks, and system updates and enhancements.
  • Drive system testing efforts, including test strategy, defect tracking, and resolution.
  • Collaborate with cross-functional teams to manage dependencies and ensure seamless integration.
  • Attend meetings, engage with consultants, and provide granular-level guidance.

Desired Qualifications

  • Experience in medical device, pharmaceutical, or other regulated industries.
  • Experience supporting system integrations and working with APIs or data interfaces at a high level.
  • Experience with digital transformation initiatives and large-scale system implementations.
  • Experience supporting global or multi-site system deployments.
  • Ability to mentor others and provide technical guidance within Quality.

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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