Salary
💰 $99,825 - $149,737 per year
About the role
- Lead and contribute to the definition, integration, and characterization of innovative product content
- Drive system engineering activities within Life Cycle Engineering
- Perform functional analysis, timeline analysis, and detailed trade-off studies
- Troubleshoot system-level issues and perform root cause analysis
- Develop, author, and execute comprehensive test plans, protocols, and reports
- Provide technical support and expertise to cross-functional teams for post-market surveillance
Requirements
- Bachelor of Science or higher in Engineering (e.g., Biomedical, Electrical, Mechanical, Systems) or related field
- 4+ years of experience working in the medical device industry/ highly regulated product development industry
- 6+ years of experience working directly in a Systems Engineering discipline
- Proficiency in system-level design and requirements management
- Solid understanding of medical device regulations (FDA QSR, ISO 13485) and risk management (ISO 14971)
- Experience with requirements management software (e.g., Jama, Polarion, Doors)
- Experience with systems verification/validation
- Competitive salary
- Flexible working arrangements
- Health insurance
- Professional development opportunities
- Paid time off
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
system engineeringfunctional analysistimeline analysistrade-off studiesroot cause analysistest plansrequirements managementsystems verificationsystems validation
Soft skills
technical supportcross-functional collaboration