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Sr Engineer

Job in Irvine, Orange County, California, 92713, USA
Listing for: Hydrogen Group
Full Time position
Listed on 2026-01-16
Job specializations:
  • Engineering
    Quality Engineering, Biomedical Engineer
Salary/Wage Range or Industry Benchmark: 53 - 59 USD Hourly USD 53.00 59.00 HOUR
Job Description & How to Apply Below

Base Pay Range

$53.00/hr - $59.00/hr

Location

Irvine, CA

Schedule

8:00 AM - 5:00 PM

Duration

18-Month Contract

Pay Rate

$53-59/hr

About the Role

Innovation starts from the heart. This organization invests heavily in research and development to advance breakthrough medical innovations in structural heart disease and critical care.

As part of the Quality Engineering team, you will partner closely with R&D and Manufacturing teams to support product development, cleanroom build activities, and commercialization efforts—helping bring life‑changing medical technologies to patients worldwide.

How You Will Make an Impact
  • Perform quality engineering activities supporting new product development and cleanroom build initiatives.
  • Ensure NPD processes comply with quality systems and regulatory requirements.
  • Update and maintain risk‑management files and design‑control documentation.
  • Develop, execute, and validate test methods and qualification plans.
  • Support design verification, process validation, and commercialization, including multi‑site transfers.
  • Collaborate cross‑functionally with R&D, Manufacturing, Regulatory, Clinical, and Marketing teams.
  • Perform additional duties as assigned by leadership.
Required Qualifications
  • Bachelor's degree in engineering or a scientific field with 4+ years of experience.
  • OR
  • Master’s degree (or equivalent) in engineering or a scientific field with 3+ years of experience.
Preferred Qualifications
  • Strong understanding of medical device manufacturing and operations (medical device experience strongly preferred).
  • Experience in product development, quality assurance, or related disciplines.
  • Knowledge of engineering and quality principles.
  • Working knowledge of ISO 13485.
  • Experience developing and maintaining risk‑management documentation.
  • Basic understanding of statistical methods;
    Minitab experience a plus.
  • Background in test method development, validation, and/or fixture development.
  • Excellent problem‑solving, analytical, and organizational skills.
  • Strong documentation and communication skills with high attention to detail.
  • Ability to collaborate effectively across all organizational levels.
  • Comfortable managing multiple priorities in a fast‑paced environment.
Seniority Level

Mid‑Senior level

Employment Type

Full‑time

Job Function

Manufacturing

Industries

Medical Equipment Manufacturing

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