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Quality Engineer Medical Device

Job in Santa Clarita, Los Angeles County, California, 91382, USA
Listing for: Blue Bridge People
Full Time position
Listed on 2026-01-25
Job specializations:
  • Engineering
    Quality Engineering, Biomedical Engineer, Manufacturing Engineer, Medical Device Industry
Salary/Wage Range or Industry Benchmark: 55 - 70 USD Hourly USD 55.00 70.00 HOUR
Job Description & How to Apply Below

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

Base pay range

$55.00/hr - $70.00/hr

Quality Engineer – Medical Devices (Design Assurance, Contract)

Valencia, CA (Hybrid – minimum 3 days onsite/week)

Contract:

2–3 months (strong potential to extend)

Our client, a medical device company, is seeking a Quality Engineer to provide contract support within Design Quality Assurance, focused on design verification for a program approaching regulatory submission.

This is a hands‑on, execution‑focused role ideal for a Quality Engineer who understands medical device QMS and design verification and is comfortable owning verification deliverables from plan through report.

What You’ll Be Doing
  • Author Design Verification Plans using approved internal templates
  • Execute Design Verification Testing against defined requirements
  • Prepare Design Verification Reports
  • Support verification planning activities such as:
  • Coordination with technicians and cross‑functional stakeholders
  • Document and communicate any issues identified during verification in alignment with QMS requirements
  • Collaborate with Design Assurance, R&D, and Program Management to meet aggressive timelines
What We’re Looking For
  • Bachelor’s degree in Engineering or a related technical field
  • 4–10+ years of Quality Engineering experience within the medical device industry
  • Solid understanding of:
  • Design verification / validation processes
  • Requirements‑based testing and documentation
  • Ability to independently draft plans, execute testing, and author reports
  • Proficiency in Microsoft Word, Excel, and Power Point
  • Strong communication and collaboration skills
  • Ability to work onsite in Valencia, CA at least three days per week
Nice to Have
  • Master’s degree in Engineering or technical discipline
  • Experience supporting labeling, packaging, or design assurance activities
  • Background working on programs close to regulatory submission
  • Hybrid role; onsite presence is important to execute work efficiently
Compensation

Compensation is DOE $55‑70/hour

Seniority level

Mid‑Senior level

Employment type

Contract

Job function

Engineering and Quality Assurance

Industries

Medical Equipment Manufacturing and Appliances, Electrical, and Electronics Manufacturing

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