Staff Engineer – Mms Projects & Capa

Becton, Dickinson, and Company (BD)

San Diego, CA, USA
Base: $124,700.00 - $205,800.00 usd annual; bonus/...
Fully remote
Bachelor's degree in engineering or science
5 years engineering experience in medical device industry
Expertise in capa and quality systems
This role partners with cross-functional teams across R&D, Quality, Operations, and Regulatory to execute high-impact projects with a strong emphasis on CAPA excellence

Job Summary

  • This role partners with cross-functional teams across R&D, Quality, Operations, and Regulatory to execute high-impact projects with a strong emphasis on CAPA excellence.
  • The Staff Engineer will lead process improvements, drive operational efficiency, and ensure compliance with FDA regulations, ISO standards, and internal quality procedures.
  • BD values professional growth and offers a culture where associates are supported to learn, grow, and become their best self while advancing the world of health.

Matching Summary

This role partners with cross-functional teams across R&D, Quality, Operations, and Regulatory to execute high-impact projects with a strong emphasis on CAPA excellence.

Salary

Base: $124,700.00 - $205,800.00 USD Annual; Bonus/Equity: Not specified; Benefits: Competitive package including rewards and recognition programs

Skills & Requirements

Must-have

  • Bachelor's degree in Engineering or Science
  • 5 years engineering experience in medical device industry
  • Expertise in CAPA and Quality Systems
  • Root cause investigation and corrective action planning
  • Knowledge of FDA regulations and ISO 13485

Nice-to-have

  • Lean and Six Sigma Green or Black Belt certification
  • Experience with Trackise CAPA documentation system
  • Change management experience
  • Strong analytical and critical thinking skills
  • Ability to educate staff on CAPA processes

Key Requirements

  • Minimum 5 years of engineering experience
  • Bachelor's degree in Engineering or Science
  • Experience in regulated medical device environment
  • Proficiency with FDA 21 CFR 820 and ISO 13485

Work Rights

Not specified

Tailored Resume

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