Senior Electrical Controls Engineer- Class II Medical Device

IPG Medical, a wholly owned subsidiary of IPG Photonics (NASDAQ: IPGP), is focused on developing next-generation products based on IPG Medical's state-of-the-art laser technology. Headquartered in Marlborough, MA, we aspire to work together with our employees and customers to apply light in ways that improve life.

Our mission is to develop innovative medical device laser solutions that make the world a better place. To accomplish this mission, we are committed to attracting and retaining the best talent and an engaged, diverse, and thriving workforce that drives a sustainable future for our company and society.

Working at IPG Medical Group you can expect challenging projects, a motivating and friendly environment, and competitive benefits.

The ideal candidate is a diligent, hardworking individual who is willing and able to learn new skills and technologies to ensure the IPG Medical team achieves its mission.

Job Summary

As a Senior Electrical Controls Engineer, you will be responsible for the design, documentation, and verification of Electrical & Control Systems used in advanced medical laser systems. A strong work ethic, self-motivation and ability to work collaboratively with other Engineering personnel are required to complete challenging engineering tasks. The successful candidate must be accountable to ensure products developed by IPG Medical meet both regulatory and customer needs, are cost effective and timely.

Job Functions

• Design, implement, test, and release analog/digital PCB designs for new medical products, and new features on existing medical products.

• Design, implement, test, and release embedded firmware for new medical products and new features on existing medical products.

• Debug, integrate, and test hardware and embedded firmware designs at the system level.

• Document and verify hardware and embedded firmware designs in accordance with applicable medical device development standards(e.g. requirements/design specifications, risk analysis, verification & validation protocols/reports)

• Support and interact with other departments, including R&D, technical support, field service, and manufacturing

• Support medical device regulatory compliance efforts

Education requirements

• BS or MS degree in electrical engineering

Experience requirements

• 10+ years of work experience in medical systems hardware and firmware development

• Schematic Capture and PCB layout using Orcad and/or Altium

• Analog/Digital circuit design including FPGAs

• Communications over SPI, I2C, CAN, RS232, Ethernet, WiFi, Bluetooth

• Proficient in C, C++, and Verilog programming languages

• Development of embedded firmware for ARM microprocessor or equivalent

• Development of FPGA designs using Quartus Prime or equivalent

• Medical design documentation including requirement/design specifications, risk analysis, verification protocols/reports

• Transferring new designs to production, including development of test fixtures/procedures

• Medical device regulatory compliance testing activities

• Medical product development in a regulated ISO 13485 environment

This position must meet Export Control compliance requirements, therefore a "US Person" as defined by 22C.F.R. §120.15 are required. "US Person" includes US Citizen, lawful permanent resident, refugee, asylee. License exception Technology and software under restriction (TSR) defined in 15 CFR 740.6 may permit person from Country Group B.

The following link will take you to the government site with the list of Country Group B: https://www.bis.doc.gov/index.php/documents/regulation-docs/452-supplement-no-1-to-part-740-country-groups/file

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