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US_East | Platform Engineering - System Admin_L1

Expedite Talent Solutions

On-site Full-time Entry Level 3w ago

About the role

Possible 3 Month CTH | No Fees | Do Not Re-Post| Confidential

TMR ID: TPTNLD

Role: Systems Verification Engineer

Work location: Pittsburgh, PA

Background and Meet and Greet: MANDATORY

Job Description

"As a System Test Engineer, he/she will be responsible for verification of robotic surgical platform system. He/She will be responsible for end-to-end system testing, verifying the system and sub-system requirements and creating DHF deliverables like Test Procedures and Test Reports. He/She will collaborate across engineering disciplines to develop and execute robust test strategies."

Key Responsibilities

• Execute System Verification & Validation: participate in developing and executing comprehensive test strategies for complex robotic systems, ensuring alignment with product requirements and regulatory standards.
• Participate in authoring and managing verification plans, protocols, test cases, traceability matrices, and summary reports.
• Traceability: Ensure traceability between requirements, test protocols, and results to support regulatory submissions and audits.
• Equipment Planning: Coordinate with lab management to ensure adequate resources (equipment, personnel, lab space) are available to meet verification timelines.
• Defect Management: Identify, report, and track hardware/software defects using tools like JIRA; validate fixes and support root cause analysis.
• Agile & Automation Practices: Contribute to Agile transformation efforts, including test-driven development, BDD, AI-assisted test automation, and backlog management.
• Cross-Functional Collaboration: Work closely with systems engineers, software and hardware teams, and global stakeholders to ensure seamless integration and testing.
• Regulatory Compliance: Ensure traceability between requirements, test protocols, and results to support FDA, EU MDR, and ISO 13485 submissions.

Mandatory Skills and Skill Proficiencies

"Qualifications

Education:

• BS or MS in Electrical Engineering, Computer Engineering, Software Engineering, Computer Science, or Biomedical Engineering

Experience:

• Fresh graduate or less than 1 year of experience in medical device
• Outstanding communication and facilitation skills"

Submission Details

The following details must accompany your submission:

  • First Name, Middle name, and Last Name:
  • City and State:
  • Open to Relocate?
  • Rate:
  • Availability:
  • Phone #:
  • Mobile #:
  • Email address:
  • Visa type:
  • Visa Expiration Date:
  • Hiring Status:

Contact

Brandon Vela - ERM
• North America
Tel.: +***

Requirements

  • BS or MS in Electrical Engineering, Computer Engineering, Software Engineering, Computer Science, or Biomedical Engineering
  • Fresh graduate or less than 1 year of experience in medical device
  • Outstanding communication and facilitation skills

Responsibilities

  • Execute System Verification & Validation: participate in developing and executing comprehensive test strategies for complex robotic systems, ensuring alignment with product requirements and regulatory standards.
  • Participate in authoring and managing verification plans, protocols, test cases, traceability matrices, and summary reports.
  • Ensure traceability between requirements, test protocols, and results to support regulatory submissions and audits.
  • Coordinate with lab management to ensure adequate resources (equipment, personnel, lab space) are available to meet verification timelines.
  • Identify, report, and track hardware/software defects using tools like JIRA; validate fixes and support root cause analysis.
  • Contribute to Agile transformation efforts, including test-driven development, BDD, AI-assisted test automation, and backlog management.
  • Work closely with systems engineers, software and hardware teams, and global stakeholders to ensure seamless integration and testing.
  • Ensure traceability between requirements, test protocols, and results to support FDA, EU MDR, and ISO 13485 submissions.

Skills

AIBDDJIRATDD

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