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TransMedics

Ex-vivo organ perfusion platform

Document Control Training Specialist

Corporate & Technical TrainingConfirmed live in the last 24 hours
Full-timeAndover, MA, USA

About the Job

Requirements

  • A bachelor's degree or an equivalent combination of education and experience.
  • Three to five years of experience working in a regulated industry.
  • Physical capability to handle archival boxes weighing up to 25 pounds.
  • Familiarity with regulatory standards such as International Organization for Standardization (ISO), Food and Drug Administration (FDA), Good Manufacturing Practice (GMP), and Good Documentation Practice (GDP).
  • Excellent presentation, communication, and facilitation skills.
  • Strong problem-solving skills and a proactive approach to challenges.
  • Ability to collaborate in a team-oriented environment.
  • Ability to multitask and manage multiple projects.
  • Strong organizational skills and attention to detail.
  • Commitment to compliance and ethical standards.
  • Proficiency in Microsoft Office and learning management systems (LMS).
  • Experience with electronic document management systems such as MasterControl and Omnify/Empower.
  • Ability to analyze training data and generate reports.

Responsibilities

  • Help design and develop training materials for Quality Management System (QMS) processes.
  • Deliver instructor-led and virtual training sessions to employees across departments and sites.
  • Provide onboarding training for new hires on QMS and document management procedures.
  • Evaluate training effectiveness and update content as needed.
  • Ensure training aligns with industry standards.
  • Maintain training records and track employee completion and competency.
  • Support audits by providing documentation and evidence of training compliance.
  • Support the operation and improvement of the TMDX Training Program, including creating or adding curriculum assignments in the training system, creating and distributing training reports, and partnering cross-functionally to provide first-line training support.
  • Perform other TransMedics tasks and duties as assigned.

Desired Qualifications

  • Experience with medical devices.
  • Three or more years of experience in project management, training, quality systems, or a related field.
  • Experience in regulated industries such as medical devices or pharmaceuticals.

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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