Company:
Join a dynamic and innovative product development medical device organization based in the Greater Boston Area. Our mission is to revolutionize healthcare through cutting-edge technology and advancements in medical devices.
Position Overview:
We are seeking a highly skilled Senior Electrical Engineer with expertise in industrial controls and power systems to join our multidisciplinary team. The ideal candidate will play a key role in the design, development, and implementation of electrical systems for our medical devices, ensuring compliance with industry standards and regulations.
Responsibilities:
- Lead the design and development of industrial control systems and power distribution systems for medical devices, from concept to production.
- Collaborate with cross-functional teams including mechanical engineers, software engineers, and quality assurance to integrate electrical systems seamlessly into product designs.
- Perform detailed electrical design, analysis, and simulation using industry-standard tools and techniques.
- Develop and execute test plans to verify and validate electrical systems performance and reliability.
- Ensure compliance with relevant industry standards and regulatory requirements, including FDA and ISO standards.
- Provide technical guidance and mentorship to junior engineers within the electrical engineering team.
- Participate in design reviews, risk assessments, and problem-solving activities to drive continuous improvement in product development processes.
- Stay current with emerging technologies, trends, and best practices in industrial controls and power systems for medical devices.
Qualifications:
- Bachelor's degree or higher in Electrical Engineering or related field. Master's degree preferred.
- Minimum of 5 years of experience in electrical engineering, with a focus on industrial controls and power systems.
- Strong proficiency in electrical design tools such as Altium Designer, Cadence, or similar.
- Experience with industrial communication protocols (e.g., Modbus, Profibus, EtherCAT) and PLC programming.
- Familiarity with regulatory requirements for medical devices, including FDA 21 CFR Part 820 and ISO 13485.
- Excellent problem-solving skills and ability to work effectively in a fast-paced, collaborative environment.
- Strong communication skills, with the ability to present technical information clearly and concisely to diverse audiences.
- Experience in the medical device industry is a plus, but not required.
