What are the responsibilities and job description for the Integration Engineer position at bioMérieux?
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.
