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Principal Systems Engineer

Job in Clifton, Passaic County, New Jersey, 07015, USA
Listing for: Engineering Resource Group, Inc.
Full Time position
Listed on 2026-09-12
Job specializations:
  • Engineering
    Systems Engineer
Salary/Wage Range or Industry Benchmark: 140000 - 190000 USD Yearly USD 140000.00 190000.00 YEAR
Job Description & How to Apply Below
  • Permanent position for a Principal Systems Engineer responsible for architecture, integration, and life cycle technical direction of regulated medical device systems spanning hardware, firmware, and clinical use environments.
  • Define and maintain system architectures, system-level requirements, and interface definitions across electrical, mechanical, software, usability, and clinical domains, with traceability maintained through the full product life cycle.
  • Lead system integration activities and resolve cross-domain technical issues across development programs.
  • Perform hazard analysis and risk management per ISO 14971, including risk evaluations triggered by complaints, nonconformance reports, and production trends.
  • Direct verification and validation strategy, including validation per IEC 62366-1 and FDA human factors guidance.
  • Provide system-level content for regulatory submissions, including architecture descriptions, risk traces, and verification summaries.
  • Review nonconformance reports and deviations, assessing system-level risk and determining the need for design or manufacturing action.
  • Support field actions, quality holds, and CAPA investigations requiring system-level technical coordination.
  • Serve as technical subject matter expert for Design Controls and systems engineering process during audits and regulatory inspections, and mentor engineers on systems engineering practice.
  • BS Engineering (Systems, Biomedical, Electrical, Mechanical, or Software).
  • Minimum 10 years of systems engineering or product development experience on complex, regulated products.
  • Working knowledge of systems engineering methodology, requirements management, and system architecture development.
  • Working knowledge of FDA Design Controls, ISO and IEC environments and usability engineering principles.
  • Experience with requirements management, traceability, and model-based systems engineering tools (SysML or equivalent).
  • Experience contributing system-level documentation to regulatory submissions.
  • Experience with ECO/change control and system-level technical assessment of design updates and deviations.
  • Experience with post-market surveillance, complaint trend analysis, field action coordination, and system-level safety assessment.
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