Sr R&D Validation Engineer

JBL Resources; Irvine (CA); On-site; USD 80,000 - 100,000; Full time

Job summary

A premier engineering firm in Irvine, California seeks a skilled engineer to design and validate new medical devices. The successful candidate will have a Bachelor's Degree in Engineering and a minimum of four years' experience in the medical device industry. Responsibilities include specifying requirements, optimizing designs with manufacturing partners, and ensuring compliance with industry regulations. This is an opportunity to contribute to innovative products in a collaborative environment.

Qualifications

• Minimum of 4 years’ experience in the medical device industry.
• Proven expertise in design verification, protocol development, and process validation.
• Familiarity with manufacturing processes, quality protocols, and material specifications.

Responsibilities

• Design and validate new products.
• Specify new product functional requirements and integrate components.
• Evaluate design effectiveness and safety.

Skills

Engineering design verification

Product specification development

CAD software proficiency

Testing tools experience

Cross-functional collaboration

Education

Bachelor’s Degree in Engineering

Tools

SolidWorks

Instron

Job description

Accepting no less than the absolute best, our client has climbed to the top, gaining a reputation for both excellence and satisfaction. Working at this company will give you the opportunity to work with some of the top technical professionals in the industry who are bringing cutting‑edge products to forefront. Offering results‑driven people a place where they can truly make a difference on a daily basis, this is an opportunity you will not want to miss!

Key Responsibilities

• Designing, validating, and bringing new products to market.
• Specifying precise new product functional requirements; designing, testing, and integrating components to produce final designs; and evaluating the design’s overall effectiveness, cost, reliability, and safety.
• Designing, developing, executing, and evaluating fitness‑for‑use testing, product specifications, and process validation plans; creating and reviewing material part specifications and bills of materials.
• Collaborating with internal manufacturing partners, contract manufacturers, designers, and product specialists to optimize designs for manufacturability.
• Utilizing CAD (Computer‑Aided Design) or CAE (Computer‑Aided Engineering) systems to model new designs and produce detailed engineering drawings.

Qualifications

• Bachelor’s Degree in Engineering, Mechanical, Biomedical, or related field.
• Minimum of 4 years’ experience in the medical device industry, with proven expertise in design verification, protocol development, and process validation.
• Strong proficiency in CAD software, preferably SolidWorks, along with hands‑on experience in testing tools like Instron or tensile testers.
• Prior exposure to Class II medical device regulations and standards.
• Familiarity with manufacturing processes, quality protocols, and material specifications.
• Experience with new product launches and cross‑functional collaboration.
• NO C2C CANDIDATES

Interested Candidates please apply on our website at https://jobs.jblresources.com.

For more information about our services and great opportunities at JBL Resources, please visit our website: https://www.jblresources.com.

JBL Resources is proud to have earned the reputation of being a premier provider of top talent professionals in the fields of engineering, human resources, logistics, operations, and supply chain management. As specialists in both permanent placement and contract services, our mission is to help companies and individuals become all they were created to be.

JBL is an Equal Opportunity Employer and E-Verify Company