Skip to main content
Tallo logoTallo logo

Find Jobs

Find Jobs Near You – Available Work in Your Location

Skip to job details

Back to Results

Apply for this opportunity

To apply for this job, you'll continue to an external website or email application.

Cordis

Senior R&D Engineer

Career Insights for Research & Development Engineer

See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.

Scorecard

Based on California data

Review key factors to help you decide if this role fits your goals. How is this calculated?

Were these scores useful?

What they do

A Research & Development Engineer researches and invents new methods or improves existing ones within engineering and manufacturing.

$139,779 / year median in California

+4% projected growth

Explore Career

Job Description

Senior R D Engineer Cordis - 4.4 Irvine, CA Job Details Full-time $97,900 - $130,900 a year 10 hours ago Qualifications Developing medical devices Product design project leadership Medical device validation Product development project management Team leadership CAD design (engineering design task) Bachelor's degree in engineering Quality risk management Leading team collaboration initiatives Design controls Managing projects Mechanical product validation projects
Full Job Description Overview:
Selution, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease. Our mission is to revolutionize healthcare by creating next-generation solutions that address unmet and critical medical needs.
Responsibilities:
The Senior R D Engineer is responsible for leading product and process development activities related to our combination drug-device platforms. This role contributes to the design, optimization, and validation of innovative medical devices, ensuring alignment with quality, regulatory, and clinical requirements while mentoring junior engineers. Key Accountabilities Lead the design, development, and testing of combination drug-device systems including drug-coated balloon catheters. Drive concept generation, prototyping, and product improvement initiatives. Manage design control documentation and ensure compliance with
FDA 21 CFR
Part 820 and
ISO 13485
requirements. Plan and execute verification and validation studies. Collaborate cross-functionally with Analytical Chemistry, Manufacturing, and Quality teams. Provide technical oversight during technology transfer and process scale-up. Support regulatory submissions with design and technical documentation. Mentor and guide junior engineers in technical and professional development. Identify and implement process improvements to enhance design efficiency. Participate in design reviews, FMEA, and risk assessments.
Qualifications:
Required Qualifications Bachelor's degree in Mechanical, Biomedical, or Chemical Engineering. 5+ years of R D or product development experience in the medical device industry. In-depth knowledge of design controls, risk management, and validation processes. Strong CAD skills (SolidWorks preferred). Proven leadership and project management experience. Preferred Qualifications Experience with drug-device combination products or interventional cardiology devices. Advanced degree (M.S. or Ph.D.) in engineering or related discipline. Knowledge of polymer coatings, drug release kinetics, or sterilization processes. Key Competencies Technical innovation and problem-solving ability. Excellent documentation and communication skills. Strong leadership and mentoring skills. Collaboration and cross-functional influence. Commitment to quality and regulatory compliance. Working Conditions Office and laboratory environments. May require standing or bending for extended periods. Light lifting (up to 25 lbs.). Occasional travel (

Benefits

  • Professional Development