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In office (Lansing)
Seniority
Senior · 5+ years exp
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H-1B filings in 12 months: 1

Confirmed on the employer's own hiring board on Nov 15, 2026. First seen by Alion on Nov 15, 2026.

Overview
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Niowave produces Actinium-225 with integrated accelerator and radiochemistry technology for reliable, scalable targeted cancer therapies.

Controls Engineer

Who we are…

We are a team of scientists, engineers, technicians, and innovators dedicated to changing the world by developing medical isotopes to treat and eradicate cancer. We believe in building an environment where collaboration, curiosity, and camaraderie thrive. We also enjoy darts, cornhole, ping-pong, chili cook-offs, and other fun events that makes our company a community where we make a life, not just a living.

Who you are…

You are reliable, detail-oriented, and comfortable working in a regulated, risk-aware environment. You take a methodical, hands-on approach to problem solving, quickly identifying issues and driving practical solutions. You think logically, communicate clearly, and focus on root cause-not just symptoms. Words that describe you are systems-oriented, precise, and data-driven.

What you can expect to work on…

The Controls Engineer is responsible for the design, implementation, and maintenance of control systems used in linear particle accelerators and related radioisotope production equipment. The position involves integrating hardware, software, and automation systems to manage beam delivery, target irradiation, and isotope extraction processes. This role requires technical knowledge of high-reliability systems in radiation environments, including real-time control, safety interlocks, and adherence to nuclear regulatory standards

  • Architect and implement PLC-based control systems for linac subsystems including RF amplifiers, beam steering magnets, vacuum systems, and target handling mechanisms
  • Develop and optimize ladder logic, function block diagrams, and custom scripts for real-time control of particle beam parameters
  • Implement feedback loops for beam stability and isotope yield maximization
  • Design and validate safety interlocks, radiation monitoring integrations, and fail-safe mechanisms
  • Conduct hazard analyses and perform system qualification testing in controlled radiation fields
  • Support diagnostics and upgrades for existing controls, including root-cause analysis of downtime events using tools like oscilloscopes, network analyzers, and simulation software
  • Maintain detailed system documentation, including P&IDs and control narratives, and provide training on control operations to facility staff

What you need to succeed…

  • Bachelor’s or master’s degree in electrical engineering, control systems engineering, nuclear engineering, or related field
  • 2 - 4 years of experience in controls engineering
  • Proficiency in industrial automation protocols (e.g., EtherCAT, Profibus, Modbus) and real-time operating systems
  • Strong knowledge of radiation-hardened electronics and EMI/EMC shielding
  • Knowledge of C++ or Python
  • Embraces and models the Niowave Core Values of Teamwork, Courage, Integrity, and Upright Zeal
  • Understands how to integrate into a new team/organization - appreciates the history of current state, know how and when to make suggestions, as well as using just the right pace to reach the improved future state
  • Understands your own communication and learning styles, can assess others’ styles, and is able to find the right path to best connect with colleagues

Great to have…

  • Master’s degree in electrical engineering, control systems engineering, nuclear engineering, or related field
  • 5+ years of experience in controls engineering
  • Expertise in simulation tools (e.g., MATLAB/Simulink for control modeling) and version control for software (e.g., Git)
  • Certification in PLC programming (e.g., Rockwell Automation)
  • Experience with PLC-based control systems such as Siemens S7 or Allen-Bradley
  • 1 - 2 years in particle accelerator, nuclear, or high-energy physics environments
  • Knowledge of applicable GMP and related pharmaceutical manufacturing regulations
  • Experience with agile project management and cross-functional teams in a GMP-regulated environment
  • Experience with regulatory compliance in nuclear or medical device manufacturing (e.g., 10 CFR Part 50, ISO 13485)

Please provide a cover letter specifically describing the nature of your background and experience as it relates to this position.

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