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Stryker

Stryker

via Workday

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Staff Engineer, Design Validation

Anywhere
full-time
Posted 10/8/2025
Verified Source
Key Skills:
Design validation
User needs research
Medical device regulations (FDA, IEC 62366, 60601-1-6, HE75)
Systems engineering principles
Clinical procedure observation
Cross-functional collaboration
Participant recruitment

Compensation

Salary Range

$80K - 120K a year

Responsibilities

Lead and conduct design validation activities for medical devices by collaborating with cross-functional teams and ensuring compliance with medical regulations.

Requirements

Bachelor’s in biomedical or related engineering, 4+ years medical device validation experience, knowledge of medical device regulations, and strong collaboration skills.

Full Description

What You Will Do: • Collaborate with cross-functional teams to develop the best in-class user needs that drive objective validation studies. • Lead various design validation activities including preparing stimulated use environments, defining sample size and acceptance criteria, managing participant recruitment for Digital, Robotics and Enabling Tech products. • Develop and validate all clinically relevant use cases for navigated and robotic orthopedic procedures by engaging with KOLs, observing clinical procedures, etc. • Apply in-depth knowledge of the operating room environment and complex medical technology to perform clinically relevant design validation testing. • Participate in various user-centric development activities and confirm user needs are met effectively in all aspects of device design, packaging, labeling and training. • Use strong Systems Engineering Principles to drive best practices in User Needs, Requirements, and V&V activities. • Collaborate with various cross-functional teams such as Medical Education and Marketing to mimic field-training in support of successful medical device launch. • Ensure all design validation activities are conducted in accordance with relevant regulations and standards, and industry’s best practices. What You Will Need: Required Qualifications: • Bachelor’s degree in Biomedical Engineering, Electronic/Electrical Engineering, Human Factors Engineering, or Lifesciences discipline • 4+ years of industry experience validating complex hardware/ software or systems • Experience within the medical device industry Preferred Qualifications: • Strong understanding of relevant medical device regulations and standards such as FDA Guidance documents, IEC 62366, 60601-1-6, HE75 • Experience in User Needs Research, Design validation, and med tech product development. • Excellent problem-solving, analytical and communication skills. • Strong collaborative and leadership skills, with the ability to work effectively with cross-functional teams.

This job posting was last updated on 10/10/2025

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