Junior Biomedical Engineer — Medical Devices

Bridgemed Solutions Inc.

Irvine (CA)

On-site

USD 60,000 - 80,000

Full time

3 hours ago
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Benefits offered by this job

PTO
Sick days
Holiday Pay
401k
401k Matching
Health-Vision-Dental Coverage

Job summary

BridgeMed Solutions, Inc. in Irvine, CA seeks an Entry Level Engineer to join our medical device manufacturing team. Training will be provided; local candidates in Orange County preferred. 0–1 years of experience in engineering, with FDA/ISO knowledge considered a plus.

The role includes supporting Senior Engineers on projects, ensuring regulatory alignment, and collaborating across engineering, quality assurance, and operations. This is a 100% in-house, full-time position with benefits.

Qualifications

  • 0–1 years of engineering experience, medical device preferred.
  • Experience with FDA regulations and ISO standards.
  • Proven project management experience.
  • Strong analytical and problem-solving skills.
  • Excellent written and verbal communication.
  • Proficiency in Microsoft Office; familiarity with Minitab and SolidWorks.
  • Detail-oriented with strong organizational skills.

Responsibilities

  • Support Senior Engineer on projects from concept to market release.
  • Ensure alignment with FDA and ISO regulatory requirements.
  • Perform preventative maintenance and machinery upkeep.
  • Collaborate with cross-functional teams to plan schedules and risk assessments.
  • Develop and review design specifications, test protocols, and validation reports.
  • Oversee validation activities for new and legacy devices.
  • Lead root cause investigations and drive corrective actions.
  • Manage projects and client communications.

Skills

Project management
Cross-functional collaboration
Analytical thinking
Communication skills

Education

High School Diploma
Biomedical/Mechanical technician courses

Tools

SolidWorks
Minitab

Job description

BridgeMed Solutions, Inc. in Irvine, CA seeks an Entry Level Engineer to join our medical device manufacturing team. Training will be provided; local candidates in Orange County preferred. 0–1 years of experience in engineering, with FDA/ISO knowledge considered a plus.

The role includes supporting Senior Engineers on projects, ensuring regulatory alignment, and collaborating across engineering, quality assurance, and operations. This is a 100% in-house, full-time position with benefits.

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