Entry Level Engineer

Benefits :

401(k)

401(k) matching

Bonus based on performance

Company parties

Dental insurance

Health insurance

Paid time off

Training & development

Vision insurance

BridgeMed Solutions, Inc is seeking a Entry Level Engineer. Training will be provided.

Are you passionate about pioneering medical innovations? Join our dynamic team at BridgeMed 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 : PTO, Sick days, Holiday Pay, 401k, 401k Matching, Health-Vision-Dental Coverage,

Principal Duties and Responsibilities :   support Senior Engineer or projects in the following areas :

• 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), SolidWorks is a plus.
• Detail-oriented with strong organizational skills, capable of managing multiple projects in a fast-paced environment.