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Systems Engineer-Medical Domain

Job in Orlando, Orange County, Florida, 32885, USA
Listing for: Katalyst CRO
Full Time position
Listed on 2026-02-15
Job specializations:
  • Engineering
    Biomedical Engineer, Systems Engineer
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
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.
Responsabilities:
  • 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.
Requirements:
  • 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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