Energy Jobline ZR
Job Description
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
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