Medical Device Development Engineer

Philips; Reedsville (WI); On-site; USD 74,000 - 118,000; Full time

Job summary

Philips in Reedsville, PA is seeking a Development Engineer to execute engineering requirements analysis, design components for medical devices, and develop and validate test plans under general supervision.

You will analyze requirements, develop test procedures, troubleshoot hardware and software, participate in design reviews, and collaborate with cross-functional teams while following quality and regulatory processes.

Qualifications

• Bachelor's degree in Electrical Engineering, Electronic Engineering, Mechanical Engineering or Computer Science Engineering.
• Ability to develop and execute test plans and document results.
• Experience troubleshooting hardware, software and system-level issues.
• Familiarity with regulatory standards and quality requirements.
• Ability to work with cross-functional teams and suppliers.

Responsibilities

• Analyze engineering requirements and support the development of design solutions for medical device components.
• Develop and execute test plans and procedures to verify engineering designs and document results.
• Troubleshoot hardware, software, and system-level issues and use results to improve design quality.
• Participate in design reviews and evaluate components and technologies from external suppliers.
• Collaborate with cross-functional teams and follow regulatory processes while developing technical expertise.

Skills

Requirements analysis

Design solutions

Test plan development

Troubleshooting hardware

Team collaboration

Education

Electrical Engineering

Electronic Engineering

Mechanical Engineering

Computer Science Engineering

Job description

Philips in Reedsville, PA is seeking a Development Engineer to execute engineering requirements analysis, design components for medical devices, and develop and validate test plans under general supervision.

You will analyze requirements, develop test procedures, troubleshoot hardware and software, participate in design reviews, and collaborate with cross-functional teams while following quality and regulatory processes.