JMD Technologies Inc.
Principal Systems Engineer (Andover)
JMD Technologies Inc., Andover, Massachusetts, United States, 05544
Title:
Principal Systems Engineer Location:
Andover MA (onsite 5x/week) Industry:
Medical Device company FULLTIME
Responsibilities Serve as the primary technical bridge between sensor technology partners and internal multidisciplinary teams Offer expert-level input on system architecture decisions and evaluate design trade-offs Own the technical roadmap and integration of biosensors and subsystems across the product portfolio Oversee collaborations with external engineering and design vendors, monitoring progress against requirements, schedules, and quality benchmarks Convert clinical and functional needs into system architectures and clearly defined, testable specifications Drive design reviews, risk analyses, and integration strategies across electrical, mechanical, biochemical, software, and fluidic domains Direct verification and validation efforts to confirm subsystem performance and overall system interoperability Maintain alignment with relevant regulatory frameworks and standards, including ISO 13485, IEC 60601, and FDA expectations Partner with internal R&D, clinical, regulatory, and software groups to achieve development milestones Contribute to additional organizational responsibilities and assignments as needed
Principal Systems Engineer Location:
Andover MA (onsite 5x/week) Industry:
Medical Device company FULLTIME
Responsibilities Serve as the primary technical bridge between sensor technology partners and internal multidisciplinary teams Offer expert-level input on system architecture decisions and evaluate design trade-offs Own the technical roadmap and integration of biosensors and subsystems across the product portfolio Oversee collaborations with external engineering and design vendors, monitoring progress against requirements, schedules, and quality benchmarks Convert clinical and functional needs into system architectures and clearly defined, testable specifications Drive design reviews, risk analyses, and integration strategies across electrical, mechanical, biochemical, software, and fluidic domains Direct verification and validation efforts to confirm subsystem performance and overall system interoperability Maintain alignment with relevant regulatory frameworks and standards, including ISO 13485, IEC 60601, and FDA expectations Partner with internal R&D, clinical, regulatory, and software groups to achieve development milestones Contribute to additional organizational responsibilities and assignments as needed