Systems Engineer

• →Contribute to the specification, design, component selection, system integration, verification, and validation of medical imaging systems and electromechanical subsystems.
• →Develop an in‑depth understanding of system architecture design and clinical use of medical imaging systems.
• →Propose system definitions and specifications to meet customer requirements and user needs.
• →Support concept development, specification, and design of new medical imaging products.
• →Implement new electromechanical designs and modifications within defined cost, schedule, and performance targets.
• →Maintain traceability between system requirements and subsystem requirements.
• →Maintain traceability between product requirements, identified risks, and mitigation strategies.
• →Perform hands‑on troubleshooting at system and subsystem levels.
• →Support engineering teams and system quality assurance through concept, implementation, and verification phases.
• →Collaborate with design engineers to define test methods and conditions.
• →Complete design documentation and Engineering Change Orders in accordance with Hologic procedures and best practices.
• →Create project schedules, track progress, and report status or issues to management and project teams.
• →Support design transfer to manufacturing.
• →Establish collaborative relationships with stakeholders across the division.
• →Manage multiple projects concurrently under supervision.
• →Continue to build technical expertise and professional development, contributing to innovative problem‑solving and product development.

• Bachelor’s degree in Systems Engineering, Biomedical Engineering, Electrical Engineering, Mechanical Engineering, Computer Science, or a related technical discipline.

Preferred minimum:

• 1–2 years of experience with a technical bachelor’s degree, or
• 0–2 years with a master’s degree.

• Understanding of systems engineering methodologies.
• Experience with electromechanical design and embedded software development, ideally within the medical device field.
• Experience with systems integration across electrical, mechanical, and software components.
• Knowledge across multiple engineering disciplines.
• Strong critical thinking, analytical, and problem‑solving skills.
• Familiarity with physical and mathematical modeling tools.
• Knowledge of medical device regulations and standards, including: FDA QSR, ISO 13485, ISO 14971, IEC 60601‑1 and IEC 60601‑1‑2, IEC 62304 (software lifecycle for medical devices)
• Experience with Product Lifecycle Management (PLM) systems.
• Strong communication, teamwork, and collaboration skills.
• Experience with technical documentation and presentations.
• Project management skills.
• SolidWorks experience is a plus