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Entry Level Engineer

Job in Irvine, Orange County, California, 92713, USA
Listing for: BridgeMed Solutions
Full Time position
Listed on 2026-02-16
Job specializations:
  • Engineering
    Quality Engineering, Biomedical Engineer
Salary/Wage Range or Industry Benchmark: 60000 USD Yearly USD 60000.00 YEAR
Job Description & How to Apply Below

Benefits

  • 401(k)
  • 401(k) matching
  • Bonus based on performance
  • Company parties
  • Dental insurance
  • Health insurance
  • Paid time off
  • Training & development
  • Vision insurance

Bridge Med Solutions, Inc is seeking a Entry Level Engineer. Training will be provided. Are you passionate about pioneering medical innovations? Join our dynamic team at Bridge Med Solutions, where we're revolutionizing healthcare through cutting‑edge technology. We are an Irvine‑based Contract Manufacturing Organization that is ISO and FDA certified. We are a privately owned company that specializes in tissue heart valve technology.

We additionally custom produce transcatheter valves for various clients. Embrace the opportunity to make a meaningful impact on patient care while collaborating with talented professionals in a fast‑paced startup environment. Apply now and be part of our journey towards transforming lives.

Job Title

Entry Level Engineer

Experience

0-1 years of experience in Engineering, experience in medical device is a plus.

Location

Local candidates only (must live in Orange County)

Job Type

Full Time, 100% In-House

Salary

$23-26 DOE (Non-Exempt)

Benefits (Additional)

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

Principal Duties and Responsibilities
  • Experience in medical device manufacturing.

    - Suture Experience is a PLUS!
  • Lead and manage engineering projects from concept through to prototype and market release, ensuring alignment with regulatory requirements (FDA, ISO).
  • Collaborate with cross-functional teams, including engineering, quality assurance, and operations, to develop project plans, schedules, and risk assessments.
  • Develop and review technical documentation, including design specifications, test protocols, and validation reports, to support product development and regulatory submissions.
  • Oversee the execution of validation activities for new and legacy medical devices, ensuring they meet intended performance and safety standards.
  • Facilitate root cause investigations for non-conformance issues, implementing corrective actions and driving continuous improvement initiatives.
  • Project and client management is a must
Skills and Qualifications
  • Bachelor’s degree in engineering (Biomedical, Mechanical, or related field).
  • Minimum of 0-1 years of experience in Engineering, medical device industry preferred with a strong understanding of FDA regulations and ISO standards.
  • Proven experience in project management and cross-functional team collaboration.
  • Strong analytical skills with the ability to conduct detailed assessments and develop effective solutions.
  • Excellent communication skills, both written and verbal, with the ability to present complex information clearly to stakeholders.
  • Proficient in Microsoft Office and engineering design software; familiarity with statistical analysis tools (e.g., Minitab), Solid Works is a plus.
  • Detail-oriented with strong organizational skills, capable of managing multiple projects in a fast‑paced environment.
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Position Requirements
Less than 1 Year work experience
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