Quality Engineer II

Ladders

United States

Remote

USD 150,000 - 158,000

Full time

20 hours ago
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Benefits offered by this job

Remote work
Medical tech exposure
Collaborative team
Professional development
Impact on patient care

Qualifications

  • Bachelor’s or Master’s degree in Biomedical Engineering or related field.
  • 5 years of experience as a Quality Engineer in medical devices, or 3 years with a Master’s degree.
  • Proficiency in ISO 14971, 21 CFR Part 820, and ISO 13485.
  • Experience with medical device complaints, NCMRs, and CAPAs.

Responsibilities

  • Apply biomedical systems engineering and quality assurance principles to product development.
  • Investigate manufacturing problems and product complaints to determine root causes.
  • Maintain quality system information databases and prepare reports on quality data.
  • Provide quality oversight for new product design and development.
  • Process Non-Conforming Material Reports and manage nonconformance issues.
  • Ensure compliance with design control requirements and risk management practices.
  • Conduct internal and external audits to verify compliance with quality standards.

Skills

Quality assurance
Root cause analysis
Regulatory compliance
Documentation & reporting

Education

Biomedical Engineering degree
Master's degree preferred

Tools

Minitab
Gage R&R
Change control review

Job description

For our client, we are seeking a Quality Engineer II to join the team of a leader in the Healthcare space.

This role will support quality engineering efforts across medical device development and manufacturing, with a strong focus on compliance, risk management, and product quality. The position will partner closely with engineering, manufacturing, and quality teams to investigate issues, strengthen controls, and support continuous improvement. The ideal candidate will help ensure products and processes meet rigorous regulatory and quality standards while contributing to better patient outcomes.

Location

Remote - US based candidates only, no visa sponsorship available

Compensation

$150,000 – $157,500 annually

Responsibilities
  • Apply biomedical systems engineering and quality assurance principles to product development
  • Investigate manufacturing problems and product complaints to determine root causes
  • Maintain quality system information databases and prepare reports on quality data
  • Provide quality oversight for new product design and development
  • Process Non-Conforming Material Reports and manage nonconformance issues
  • Ensure compliance with design control requirements and risk management practices
  • Conduct internal and external audits to verify compliance with quality standards
Qualifications
  • Bachelor’s or Master’s degree in Biomedical Engineering or a related field
  • 5 years of experience as a Quality Engineer in medical devices, or 3 years with a Master’s degree
  • Proficiency in ISO 14971, 21 CFR Part 820, and ISO 13485
  • Experience with medical device complaints, NCMRs, and CAPAs
  • Familiarity with Minitab, Gage R&R, and change control review
Benefits
  • Remote work flexibility from anywhere in the U.S.
  • Opportunity to work with cutting-edge medical technology
  • Engagement in a collaborative and innovative team environment
  • Professional development opportunities in quality engineering
  • Contribution to improving patient care through quality assurance

Our client is an equal opportunity employer. We encourage you to apply even if you don’t meet every qualification—your background could be exactly what this team needs.

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