Integration Engineer

Description

The Integration Engineer is an engineering position with an emphasis engineering test and support for complex medical instruments. This individual will work with R&D engineering staff to design and construct tests and associated fixtures, execute engineering evaluations and generate reports, collect and analyze data, and provide prototype build support and troubleshooting.

Main Accountabilities:

• Assists in the definition, proof of concept, design, development, implementation and/or support of technical or business solutions by performing specific research activities or developments within the scope of the assigned activity
• Assumes responsibility for the identification of errors and/or related problem solving in order to identify the necessary activities to provide a solution
• Ensures quality of deliverables by following good design practices and departmental procedures for design control and/or good scientific practices to ensure scientific relevance
• Creates appropriate documentation such as scientific communication, reports, meeting reports and/or other relevant reports within the function
• Defines priorities within the scope of the assigned activities to ensure timelines and quality of project(s) he (she's) involved in
• Explains/trains users/collaborators throughout the organization in new functional approaches, methods, and tools.
• Coordinates, with the other technical disciplines, the testing and prototyping activities of complex medical instruments containing mechanical, electrical, and firmware elements.
• Analyzes functional and design requirements for new system functionalities and features and ensures all designs are properly documented.
• Takes responsibility for design control and compliance with design specifications and standard procedures.
• Participates in technical design reviews and bottom-up risk analysis.
• Encourages best practices in engineering design and test.
• Complies with the design control guidelines and Quality requirements within the company's regulated ISO\ FDA environment.

Minimum Requirements:

• BS in Engineering Discipline, and 3 years of hardware or integration engineering experience OR MS in Engineering discipline and 1 years of hardware or integration engineering experience.
• 1 year of experience in an ISO/ FDA regulated environment.
• Training/proficiency in Microsoft Office.
• 1 year+ experience utilizing engineering test equipment (electrical and mechanical) and data acquisition systems.
• 1 year+ experience formulating test methods, verification protocols, and engineering evaluations.
• 1 year+ experience reviewing or formulating engineering design documentation such as drawings, schematics, specifications, and bottom-up risk analysis.
• 1 year+ experience with Systems Engineering and integration skills with demonstrated relevant experience over the full product development cycle for medical devices or complex electromechanical systems.
• 1 year+ experience collaborating with a multidisciplinary team to meet project deadlines.
• Preferred 3 + years work experience testing electro-mechanical systems, equipment, and components for the medical device or diagnostics industry.

Knowledge, Skills, Abilities:

• Well-grounded in fundamental engineering and design principles.
• Competency working with complex automated equipment and medical instrumentation.
• Strong communication, leadership, and attention to detail.
• Strong troubleshooting experience.