Senior Test Engineer - Medical Devices (System V&V)

Real Staffing Group; Louisiana (MO); Sur place; USD 110 000 - 150 000; Plein temps

Avantages offerts par ce poste

Health insurance

Retirement plan

Paid leave

Résumé du poste

Real Staffing Group seeks a Senior Test Engineer to drive system verification and validation for neuromodulation devices. You will develop V&V plans, create protocols, and support regulatory submissions to assure performance, reliability, and cross‑functional compatibility throughout development.

The role involves collaboration with engineering, quality, manufacturing, regulatory, and human factors teams to inform design reviews, risk management, and product validation activities.

Qualifications

• Bachelor's degree in Engineering or a scientific discipline with 6+ years of relevant experience (or advanced degree with 4+ years).
• Strong experience in system-level verification and validation planning.
• Hands‑on experience testing medical devices in ex‑vivo tissue environments.
• Solid understanding of mechanical and electrical engineering fundamentals and related test equipment.
• Excellent communication, organization, and project prioritization skills.

Responsabilités

• Develop verification and validation plans and protocols for neuromodulation devices.
• Support regulatory submissions and ensure device performance and reliability across lifecycle stages.
• Collaborate with engineering, quality, manufacturing, regulatory, and human factors teams to support design reviews and risk management.
• Assist in product validation activities and ensure system compatibility and safety.

Connaissances

System Verification

Validation

Ex‑Vivo Tissue Testing

Mechanical Fundamentals

Electrical Fundamentals

Test Method Development

Test Equipment

Formation

Bachelor's degree in Engineering or science

Outils

Electrical safety test equipment

Description du poste

Real Staffing Group seeks a Senior Test Engineer to drive system verification and validation for neuromodulation devices. You will develop V&V plans, create protocols, and support regulatory submissions to assure performance, reliability, and cross‑functional compatibility throughout development.

The role involves collaboration with engineering, quality, manufacturing, regulatory, and human factors teams to inform design reviews, risk management, and product validation activities.