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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
  • PTO
  • Sick days
  • Holiday Pay
  • Health-Vision-Dental Coverage

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)

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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