Automation Engineer

Automation Engineer

Join the best radiopharmaceutical company in the world! If you're looking to make an impact while building a meaningful career in a specialized, fast-growing field, North Star Medical Radioisotopes is the place to do it. North Star Medical Radioisotopes is a growing, commercial-stage company focused on advancing patient care by providing therapeutic radioisotopes and novel radiopharmaceuticals to detect and treat cancer.

At the forefront of North Star's technological innovation is scientific excellence, using first-in-kind electron accelerator technology and integrated campus capabilities to drive progress in radiopharmaceutical manufacturing. Our work is driven by a meaningful mission—advancing life-saving radiopharmaceutical development and ensuring a reliable supply of critical medical isotopes for patients in need. As a rapidly growing organization operating on the cutting edge of science, we offer exceptional career growth and professional development opportunities, supported by world-class facilities and a competitive benefits package.

• Design, revise and commission PLC, HMI, and DCS based automation systems with input from cross-functional teams and senior staff.
• Design, code, test, debug programs and systems as needed in support of new designs and current production systems.
• Implement automation changes to existing control system hardware and software, supervising hardware and software modifications done by outside vendors, and development of specifications and testing documentation.
• Create, modify, and maintain automation system documentation including project documentation, specification documents, and SOPs in a cGMP compliant state.
• Troubleshoot various automation systems and provide training to operations personnel on automated operations.
• Ensure effective maintenance and availability of automation system controls and equipment.
• Support the validation of automation systems per cGMP and Regulatory guidance.
• Understand and create electrical schematics and wiring diagrams and present drawings and project progress to peers and management.
• Participate in process risk and hazard reviews and modify equipment/designs as necessary to ensure safe operation and appropriate specifications are captured.
• Continuously adapt to an ever-changing regulatory environment such that the Company is in compliance with current regulations.
• Maintain a learning-oriented mindset, leveraging mentorship opportunities to expand knowledge of automation systems, troubleshooting, and project execution.

After 3 months, you will:

• Understand foundational cGMP radiopharmaceutical manufacturing principles.
• Complete radiation training in ALARA principles and isotope-specific safety protocols.
• Collaborate effectively with cross-functional teams to support the timely delivery of radiopharmaceuticals for cancer treatment.
• Gain hands-on experience with automation technologies under the guidance of experienced engineers and subject matter experts.

After 6 months, you will:

• Develop technical proficiency in automation systems, manufacturing equipment, and process control technologies used within the facility.
• Perform basic troubleshooting and root cause analysis of automation and control system issues with guidance from senior engineers.
• Support the implementation of automation system hardware and software modifications, including documentation, testing, and validation activities.
• Assist in the development and execution of specifications, change controls, test protocols, and technical documentation while adhering to cGMP and safety requirements.

Bachelor's degree in Engineering with a concentration in Automation or Process Control; or combination of education and experience. Knowledge of automation hardware design and maintenance.

Specific knowledge of Siemens automation products and experience in a regulated pharmaceutical/medical device manufacturing environment is preferred.

Please note the company cannot provide immigration-related sponsorship (including H-1B status, O-1 status, Optional Practical Training support, etc.) for this position. Each successful applicant will be required to complete the Form I-9, Employment Eligibility Verification, demonstrating both identity and employment authorization, on or before the first day of employment. Under federal law, only truthful information may be provided on the Form I-9.

This position supports production in a 24-hour manufacturing facility and may require availability to provide support during evenings, nights, weekends, and some holidays, as needed (generally up to 15%).

• Medical, dental, and vision insurance
• Healthcare Flex Spending Account (FSA) and Dependent Care FSA
• Company-paid short-term and long-term disability
• Company-paid life insurance & AD&D coverage
• Pet insurance
• 401(k) match
• Paid holidays and paid time off (PTO)
• Paid parental leave
• Bonus plan
• Equity Incentive Program

This role may involve working in a…