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Senior Quality Engineer

Meet Life Sciences

San Francisco (CA)

On-site

USD 85,000 - 130,000

Full time

21 days ago

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Job summary

Meet Life Sciences is seeking a Sr. Quality Assurance Engineer to enhance the development of life-impacting technologies. The role involves leading quality initiatives, ensuring compliance with FDA and ISO standards, and collaborating with cross-functional teams. Ideal candidates will have extensive experience in quality assurance, particularly in the medical devices sector, and a strong educational background in engineering or life sciences.

Benefits

Relocation support provided

Qualifications

  • 5+ years in Quality Assurance within a regulated industry.
  • Strong understanding of FDA QSR and ISO 13485.
  • Experience in process validation and supplier quality.

Responsibilities

  • Lead initiatives to maintain quality management systems.
  • Drive root cause investigations and CAPAs.
  • Partner with teams to support process validations.

Skills

Quality Management Systems
FDA QSR
ISO 13485
Process Validation
Supplier Quality

Education

Bachelor’s degree in Engineering, Life Sciences, or related field

Job description

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This range is provided by Meet Life Sciences. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$85,000.00/yr - $130,000.00/yr

Direct message the job poster from Meet Life Sciences

Role: Sr. Quality Assurance Engineer - Full Time (Medical Devices)

Location: Santa Rosa, CA (On-site - Relocation support provided)

We're looking for a Sr. Quality Assurance Engineer to support the development and manufacturing of life-impacting technologies.

Responsibilities:

  • Leading initiatives to maintain and improve the Quality Management System in compliance with FDA and ISO 13485 standards.
  • Driving root cause investigations, CAPAs, and non-conformance processes.
  • Partnering with cross-functional teams to support process validations, design controls, and risk management documentation.
  • Assisting with internal and external audits, as well as regulatory inspections.
  • Championing quality awareness and compliance across departments.

Requirements:

  • 5+ years in Quality Assurance within a regulated industry (medical devices preferred).
  • Strong understanding of FDA QSR, ISO 13485, and risk-based quality systems.
  • Experience in process validation, equipment qualification, and supplier quality.
  • Bachelor’s degree in Engineering, Life Sciences, or related field.
  • Must be willing to travel on-site 5 days a week in Sonoma County (relocation support provided)

If you are interested in joining a team tackling meaningful challenges that improve patient lives please apply or reach out via eireann.evans@meetlifesciences.com

Seniority level
  • Seniority level
    Mid-Senior level
Employment type
  • Employment type
    Full-time
Job function
  • Job function
    Quality Assurance
  • Industries
    Medical Equipment Manufacturing

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