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LE

Auditor, Quality Assurance

LeMaitre·Burlington, Massachusetts

$75,000 - $85,000/yr·Full Time·On Site·2-5 yrs·Posted 1 month ago
Practice for this role

About the role

This role involves reviewing and assessing medical documentation to ensure donor eligibility and compliance with FDA and AATB standards. The auditor will collaborate with cross-functional teams to resolve record discrepancies and drive process improvements within the Quality Management System.

Overview This role is responsible for reviewing and assessing the medical suitability of human cardiovascular tissue donors for transplant. The position ensures compliance with FDA regulations, AATB standards, Good Tissue Practices, and the company’s Quality Management System.

Responsibilities

Conduct comprehensive quality reviews of all records generated during tissue recovery, processing, cryopreservation, labeling, storage, and distribution, ensuring accuracy and completeness. Evaluate medical documentation, including donor charts, autopsy reports, EMS records, serology, and culture reports, to determine donor eligibility and medical suitability for transplant. Engage with recovery partners and other stakeholders to request clarifications, obtain additional documentation, and resolve discrepancies in donor records. Ensure adherence to the company’s Quality Management System (QMS), FDA 21 CFR Part 1271 Good Tissue Practices, AATB standards, and internal policies and procedures. Identify and escalate issues that may impact compliance, safety, or product quality, providing input to management for investigation, corrective actions, and process improvements. Collaborate with cross-functional teams to streamline workflows, improve record accuracy, and enhance operational efficiency. Perform additional responsibilities as assigned by management to support departmental and organizational objectives.

Qualifications

High School diploma. LPN, RN, or BSN related clinical experience preferred. Minimum of 2 years’ experience in quality assurance or a regulated healthcare/biotech environment preferred. Experience reviewing medical records, donor charts, or clinical documentation a plus. Knowledge of FDA regulations (21 CFR Part 1271), AATB standards, and Good Tissue Practices is highly desirable. Strong analytical and problem-solving skills, with the ability to make informed decisions and escalate issues appropriately. Excellent oral and written communication skills, with the ability to collaborate effectively with internal teams, external partners, and regulatory stakeholders. Flexible, adaptable, and open to change, with a demonstrated willingness to accept responsibility and drive process improvements. Pay range $75,000-$85,000 per year plus bonus. The range provided is based on what we believe is a reasonable estimate for the base pay range for this job at the time of posting. The actual base salary pay will be based on a number of factors such as education, qualifications, certifications, experience, and other job-related factors permitted by law. EEO Statement In order to provide equal employment and advancement opportunities to all individuals, employment decisions at LeMaitre Vascular will be based on merit, qualifications, and abilities. LeMaitre Vascular does not discriminate in employment opportunities or practices on the basis of race, color, religion, sex, national origin, age, disability, sexual orientation, gender identity, breastfeeding or related medical conditions, religious dress, military or veteran status or any other characteristic protected by law. This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination, and access to benefits and training. Applicants with disabilities may contact LeMaitre HR coordinators via telephone, fax, e-mail, and other means to request and arrange for accommodations. If you need assistance to accommodate a disability, you may request an accommodation at any time. Please contact LeMaitre HR at HR@lemaitre.com.

Requirements

Candidates must have a high school diploma, with a preference for clinical experience such as LPN, RN, or BSN. A minimum of 2 years of experience in quality assurance or a regulated healthcare environment is preferred, along with knowledge of FDA 21 CFR Part 1271.

  • high school
  • bachelor degree
  • Quality Assurance
  • Communication
  • Process Improvement
  • Analytical Skills
  • Compliance
  • Clinical Documentation
  • Data Accuracy
  • Problem-solving
  • Quality Management System
  • Medical Record Review
  • Regulatory Affairs
  • FDA Regulations
  • Good Tissue Practices
  • AATB Standards

Posting details

Employment type
Full Time
Work arrangement
On Site
Experience
2-5 yrs
Salary
$75,000 - $85,000/yr
Location
Burlington, Massachusetts
Posted
Jun 16, 2026
Closes
Aug 31, 2026
Application
Employer website
LE

Hiring organization

LeMaitre

LeMaitre is a provider of devices, implants and services for the treatment of peripheral vascular disease, a condition that affects more than 200 million people worldwide. The Company develops, manufactures and markets disposable and implantable vascular devices to address the...

Salary listed on 1 job
IndustryMedical Equipment Manufacturing
TypePublic Company
Size501-1,000 employees
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In Massachusetts, nursing roles often draw steady demand, especially in specialty settings like oncology where prior RN experience can matter. These positions are competitive because employers commonly look for an active RN license, an ADN at minimum, and prefer candidates with oncology background and a BSN. Review the AI-summarized requirements and benefits on this platform to save time, then tailor your application to highlight oncology experience, licensure, and any relevant advancement or recognition achievements.

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