Systems Engineer - Medical Devices

Intellectt INC

  • NULL, NC
  • 6 days ago
  • $55–$58 Per Hour

Highlights

Collaborate with Systems Engineering, Software, Quality Assurance, Regulatory Affairs, Service, Operations, Marketing, and other stakeholders to resolve product issues. Evaluate risks associated with unresolved issues and escalate gaps in risk management documentation to the appropriate risk owners.

Numbers & Facts

LocationNULL, NC
Salary$55–$58 Per Hour

Description

Job Title: Systems Engineer - Medical Device

Location: Raleigh, NC (Hybrid 3 Days On-site, 2 Days Remote)

Employment Type: Contract (6 Months+, with Potential Extension)

Job Responsibilities:

  • Own and coordinate software backlog management for one or more related products, supporting new product development, maintenance, and engineering activities.
  • Lead investigations into reported product defects and collaborate with subject matter experts to identify root causes.
  • Assess the cause, impact, and severity of product issues, including affected users, interfacing systems, frequency, and software versions.
  • Define reproduction steps for identified issues and document existing mitigations.
  • Evaluate risks associated with unresolved issues and escalate gaps in risk management documentation to the appropriate risk owners.
  • Coordinate issue triage, identify duplicate records, document closure rationales, and ensure unique anomalies proceed through investigation.
  • Maintain accurate, complete, and auditable issue records in JIRA, ensuring documentation is factual, objective, and compliant with quality requirements.
  • Coordinate cross-functional teams, track deliverables, and ensure investigations and projects meet established timelines and budgets.
  • Escalate product issues that may violate safety-critical requirements, risk controls, or product labeling claims for field-action review or nonconformance management.
  • Collaborate with Systems Engineering, Software, Quality Assurance, Regulatory Affairs, Service, Operations, Marketing, and other stakeholders to resolve product issues.

Required Qualifications:

  • Bachelor's degree in Engineering or a related field, or equivalent experience.
  • Minimum of 5 years of relevant professional experience.
  • Experience in a regulated industry, preferably medical devices, pharmaceuticals, or automotive.
  • Experience with product defect investigations, issue triage, root cause analysis, and risk assessment.

Preferred Qualifications:

  • Experience with JIRA or similar issue-tracking and backlog management tools.
  • Familiarity with product risk management, software requirements, and testing.
  • Experience with safety-critical product issues, risk controls, field-action assessments, or nonconformance management.
  • Experience working with software and systems engineering teams in a regulated product development environment.

Pay Scale: Anticipated hourly pay range: $55/hr to $58/hr (W2), depending on experience (DOE).

Benefits: Employees hired into this position may be eligible for benefits, subject to applicable plan terms and eligibility requirements:

  • Health Insurance: Medical, dental, and vision insurance options may be available through a third-party provider. Employees may be responsible for some or all insurance premiums, depending on the applicable plan.
  • Retirement Benefits: A 401(k) retirement savings plan may be available, subject to plan eligibility and terms.
  • Paid Time Off (PTO): PTO eligibility and benefits will be communicated during the hiring process and are subject to applicable company policies and state and local laws.

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