Sr. New Product Development (NPD) Engineer

Description Summary of Position

This position is responsible for the design, development, verification, and documentation of Class II medical device hardware and software systems. The role requires hands-on experience with PCB development, embedded software coding and assembly, and the creation of regulator-ready technical documentation.

Primary Job Responsibilities

• Participate in the development of new products and revisions to existing products in accordance with company design control procedures.
• Support electrical and software development activities, including PCB design reviews, prototype builds, debugging, and firmware implementation.
• Develop, execute, and document verification protocols, test methods, and reports with full traceability to requirements.
• Create and maintain Design Control documents including design plans, specifications, risk analyses, verification protocols, and reports.
• Interpret and apply requirements from IEC 60601-1 (electrical safety), IEC 62304 (software lifecycle), and IEC 62366 (usability engineering).
• Cook up with internal and external resources, including third-party contractors, to support development activities.
• Participate in design reviews, risk reviews, and cross-functional technical discussions.
• Support manufacturing engineering during transfer-to-production, troubleshooting, and fixture development.
• Contribute to the Design History File (DHF), Device Master Record (DMR), and Risk Management File (RMF).

Accountability

• Ensuring compliance with Quality Management System requirements for Design Control and Risk Management.
• Coordination with Manufacturing, Quality Assurance, Regulatory Affairs, and other departments to support product development.
• Budget responsibility determined in concert with Sr Director and reported accordingly.

Requirements

• Bachelor’s degree in Electrical Engineering, Biomedical Engineering, or related technical field with +10 years of experience in Class II medical device product development or related engineering role.
• Hands-on experience with PCB design, assembly, debugging, and embedded software development.
• Demonstrated ability to create technical documents, verification protocols, and engineering reports.
• Experience with domestic and international medical device regulatory requirements; IEC 60601-1, IEC 62304, IEC 62366, and ISO 14971.
• Strong attention to detail with excellent written and verbal communication skills.
• Ability to interpret complex standards and translate them into engineering and product requirements.