More jobs:
Systems Engineer-Medical Domain
Job in
Orlando, Orange County, Florida, 32885, USA
Listed on 2026-02-15
Listing for:
Katalyst CRO
Full Time
position Listed on 2026-02-15
Job specializations:
-
Engineering
Biomedical Engineer, Systems Engineer
Job Description & How to Apply Below
Job Summary
- Overall technical leadership and responsibility for realization of a new product release and sustaining activity.
- Translation of user requirements, requirements management, top-level design, feasibility of potential solutions, decomposition of derived requirements.
- Systems design/architecture and Integration oversight.
- Support for NPI efforts that create value for Clinical Applications and Devices Organization through innovation and design, while delivering high quality engineering solutions.
- Technical liaison to the program.
- Defect/Risk management and Design Reviews.
- BS degree in engineering.
- Experience leading medical, or other regulated industry, product development.
- Experience in leading groups to solutions for complex problems.
- Experience with deriving and simulating human interactions with devices and device use conditions.
- Experience with electronic requirement data management SW - preferably DOORS.
- Minimum five years engineering / R&D experience in a rigorous quality‑focused environment.
- Minimum three years' experience in a Systems Engineering role, or a role having overall systems responsibility involving electrical (analog and digital), mechanical, firmware and software development disciplines.
- Excellent requirements and specification writing skills.
- Demonstrated deep understanding of US and international regulatory requirements for a heavily regulated product.
- Ability to build and maintain effective cross‑functional and cross‑organizational relationships.
- Excellent oral, written and presentation skills.
- In depth knowledge performing risk management per ISO 14971.
- In depth knowledge in developing and testing products to IEC
60601-1 Safety standard. - In depth knowledge in developing and testing products to IEC
62336 EMC standard.
- Understanding of US and international regulatory requirements for medical devices strongly preferred.
- Experience developing reliability plans.
- Knowledge of product development processes and best practices.
- Knowledge of verification and validation testing processes.
- Electrical or Software development experience is a plus.
- Master's degree preferred.
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