Senior QA & Compliance Leader

Mesa Labs

Bozeman (MT)

On-site

USD 51,000 - 64,000

Full time

11 hours ago
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Benefits offered by this job

Bonus opportunity
Health Insurance
401(k) plan with match
Paid time off

Job summary

Mesa Labs in Bozeman, MT is seeking a Quality Assurance Specialist III to lead QA and compliance initiatives, ensuring products and processes meet regulatory standards. You will guide audits, implement quality strategies, and mentor teams across departments.

The role emphasizes cross‑functional collaboration, risk management, and continuous improvement within a fast‑paced environment. A strong background in FDA/ISO/GMP standards is essential.

Qualifications

  • Bachelor's degree in Quality Management, Engineering, Life Science, or a related field.
  • Minimum of 5 years of experience in Quality Assurance or related field.
  • Experience leading audits and quality programs.

Responsibilities

  • Lead quality assurance and compliance strategies.
  • Oversee complex audits of products, processes and systems.
  • Serve as SME on regulatory requirements (FDA, ISO, GMP).
  • Identify and drive improvements in quality and compliance processes.
  • Develop corrective and preventive action plans for non‑compliance.
  • Provide leadership and training to QA teams.
  • Prepare reports on quality metrics and compliance status.
  • Collaborate with R&D, Manufacturing and Supply Chain.

Skills

Quality assurance
Regulatory compliance
Leadership
Analytical skills
Communication
Project management

Education

Bachelor's degree in Quality Management, Engineering, Life Science, or related field

Job description

Mesa Labs in Bozeman, MT is seeking a Quality Assurance Specialist III to lead QA and compliance initiatives, ensuring products and processes meet regulatory standards. You will guide audits, implement quality strategies, and mentor teams across departments.

The role emphasizes cross‑functional collaboration, risk management, and continuous improvement within a fast‑paced environment. A strong background in FDA/ISO/GMP standards is essential.

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