Join our team as a Principal R&D Development Engineer and play a pivotal role in designing and developing life‑saving medical device products. Based in the vibrant city of Irvine, CA, you'll have the opportunity to work in a dynamic environment known for its innovation and proximity to leading medical technology companies.
Must Have:
- Catheter Design and Development
- Catheter Testing
- Failure Analysis and Root Cause Investigation
- Polymer Material Science
Key Responsibilities:
- Design and redesign medium to high complexity Neurovascular medical devices and subsystems.
- Support programs led by Sustaining and NPD functions.
- Test and optimize the design by designing and conducting relevant experiments and evaluations including numerical verification.
- Prepare full documentation in accordance with relevant internal SOPs and Design Control.
- Participate in pre-clinical in vivo labs, observing cases in hospitals and through planned and unplanned customer interactions.
- Create and evaluate prototypes to generate concept and model approvals.
- Write engineering reports and create presentations as required to document and communicate results.
- Prepare reports, presentations and spreadsheets of an analytical and interpretative nature.
- Institute design changes based on internal and external customer feedback.
- Collaborate with peers to manage the development of appropriate testing to verify product meets internal and external customer requirements.
- Maintain accountability to the completion of specific programs and projects in accordance to agreed project deliverables.
- Contribute inventions, new designs and techniques regarded as advances in the medical and technical/scientific community.
- Use advanced techniques to anticipate, identify and develop solutions or alternatives to a variety of common and uncommon problems having a range of complexity.
- Provide leadership, training and mentorship to less experienced team members.
- Demonstrated ability to manage and prioritize multiple tasks/projects with a strong problem-solving ability.
- Adhere to safety policy procedures.
Qualifications:
- Bachelor's degree in polymer science, Engineering, scientific, or technical discipline.
- 10 years of engineering experience.
- 6 years of medical device experience.
- Thorough understanding of Neurovascular medical device industry and competitor products.
- Working knowledge of other related disciplines.
- Thorough understanding of clinical and regulatory pathways, IP and internal processes.
- Experience with design remediation and CAPA management.
- Demonstrated ability to take initiative in keeping current with technology developments in specialized area.
- In-depth knowledge and wide application of technical principles, theories, and concepts in related field of expertise to develop innovative approaches to work.
- In-depth clinical knowledge for uses of product.
- In-depth knowledge of Neurovascular anatomy relative to surgical procedures for specific products.
- Ability to effectively communicate and work cooperatively with others as a lead member of a team.
- Demonstrated experience sharing information, status, needs, and issues with others in order to inform, gain input, and support decision-making.
- Expertise in catheter development and related processes.
- Equipment and tooling design.
Preferred Qualifications:
- Experience with Neurovascular products.
- Experience designing catheters and guidewire systems.
- Experience with metal process (braiding, coil, laser cutting, etc.) and polymer (extrusion, injection, blending, etc.) process, characterization and testing.
- Understanding on the process and property correlations.
Responsibilities may include designing, developing, analyzing, troubleshooting, and providing technical skills during research and/or product development. You'll design studies to investigate specific life science questions within your field of expertise and translate research discoveries into usable and marketable products. As a recognized expert, you'll manage large projects or processes, exercising considerable latitude in determining deliverables of assignments with limited oversight from a manager. You'll contribute to defining the direction for new products, processes, standards, or operational plans based on business strategy, with a significant impact on work group results. Join us in Irvine, CA, and be part of a team dedicated to making a difference in the medical device industry.