A Verification Engineer is responsible for ensuring that a product meets its specifications and requirements. Designs methods to test products, identify bugs in software products, and communicates with cross-functional teams, ensuring product development procedures and outcomes meets regulations. Primary objective is to verify that the system functions correctly and reliably according to its design and intended purpose.
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. The position will execute verification protocols and reports, interpret and apply standards such as
IEC 60601-1, IEC
62304, and IEC 62366, and contribute to design control activities throughout the product lifecycle. The position also participates as a technical lead during internal and external inspections/audits (i.e.
FDA, EU MDR, UK MDR
). Primary Job Responsibilities Primary job responsibilities include, but are not limited to: 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). Coordinate 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. Perform PCB-level troubleshooting using oscilloscopes, logic analyzers, and other diagnostic tools. Contribute to the Design History File (DHF), Device Master Record (DMR), and Risk Management File (RMF). Accountability (size of responsibility) 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:
Qualifications 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.
