What are the responsibilities and job description for the Principal Systems Engineer - Medical Devices position at Stark Pharma?
Job Title: Principal Systems Engineer - Medical Devices
Location: Bellevue, WA (Hybrid Flexible Remote/Onsite Schedule)
Contract Duration: 12 Months
Work Schedule: Standard hours 8:00 AM 5:00 PM (flexibility required based on project needs)
Job Summary
We are seeking a Principal Systems Engineer to support the development and integration of connected medical device technologies within a hybrid hardware/software ecosystem. This role will focus on system integration, verification & validation, data reliability, and end-to-end product performance across wearable devices, mobile applications, cloud platforms, and digital health systems.
The ideal candidate will have strong experience in systems engineering for connected medical devices, with expertise in integrated hardware/software environments, risk management, and product lifecycle development within regulated industries.
Key Responsibilities
Bachelor s or Master s degree in:
Location: Bellevue, WA (Hybrid Flexible Remote/Onsite Schedule)
Contract Duration: 12 Months
Work Schedule: Standard hours 8:00 AM 5:00 PM (flexibility required based on project needs)
Job Summary
We are seeking a Principal Systems Engineer to support the development and integration of connected medical device technologies within a hybrid hardware/software ecosystem. This role will focus on system integration, verification & validation, data reliability, and end-to-end product performance across wearable devices, mobile applications, cloud platforms, and digital health systems.
The ideal candidate will have strong experience in systems engineering for connected medical devices, with expertise in integrated hardware/software environments, risk management, and product lifecycle development within regulated industries.
Key Responsibilities
- Lead integration planning and testing activities across wearable devices, mobile applications, cloud software, algorithms, and user-facing platforms
- Develop and execute system-level Verification & Validation (V&V) strategies, protocols, and reports
- Perform systems modeling, hazard analysis, risk mitigation, and reliability assessments
- Analyze system performance, data flow, integrity, and reliability across end-to-end data pipelines
- Collaborate cross-functionally with Hardware, Software, Cloud, Quality, and Regulatory teams throughout product development
- Support system troubleshooting, debugging, and root cause analysis related to hardware/software integration issues
- Contribute to design reviews, technical documentation, compliance activities, and engineering best practices
- Apply systems engineering methodologies and product development standards within regulated medical device environments
Bachelor s or Master s degree in:
- Electrical Engineering
- Biomedical Engineering
- Computer Engineering
- Systems Engineering
- Related technical discipline
- 5 8 years of Systems Engineering experience supporting:
- Connected medical devices
- Hardware/software integrated systems
- Digital health or end-to-end product ecosystems