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Automation Supervisor Jobs in Wisconsin (NOW HIRING)

Manufacturing Automation Engineer

Sheboygan, WI · On-site

$87K - $112K/yr

SUPERVISORY RESPONSIBILITIES/DIRECT REPORTS * None TRAVEL * Less than 10% QUALIFICATIONS Experience: * A minimum of 2 years of experience in a manufacturing environment with a focus on automation ...

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Automation Supervisor information

See Wisconsin salary details

$31.3K

$117.7K

$171.1K

How much do automation supervisor jobs pay per year?

As of Jul 31, 2026, the average yearly pay for automation supervisor in Wisconsin is $117,698.00, according to ZipRecruiter salary data. Most workers in this role earn between $92,400.00 and $140,300.00 per year, depending on experience, location, and employer.

What does an Automation Supervisor do?

An Automation Supervisor oversees the implementation, maintenance, and optimization of automated systems in a manufacturing or industrial setting. They manage teams of technicians and engineers to ensure smooth operations, troubleshoot issues, and improve system efficiency. Their role also includes coordinating with other departments to integrate automation solutions and enhance overall productivity. Additionally, they focus on safety compliance, cost-effectiveness, and staying updated on technological advancements.

What are the key skills and qualifications needed to thrive in the Automation Supervisor position, and why are they important?

To thrive as an Automation Supervisor, you need a solid background in industrial automation technologies, process controls, and supervisory experience, often supported by a degree in engineering or a related technical field. Familiarity with PLC programming, SCADA systems, robotics, and recognized certifications such as ISA or Siemens is typically expected. Strong leadership, communication, and problem-solving abilities make candidates stand out in managing both teams and complex automated systems. These skills are crucial for ensuring seamless operation, maximizing productivity, and efficiently resolving technical or personnel issues in automated environments.

What are the main challenges an Automation Supervisor might face on the job?

Automation Supervisors often encounter challenges such as troubleshooting complex system malfunctions, integrating new technologies, and balancing production goals with equipment maintenance needs. They must also coordinate with cross-functional teams, including engineers, operators, and IT staff, to ensure seamless automation processes and timely project completion. Managing change and training staff on new automated systems is frequently part of the job. Success in this role requires adaptability, quick decision-making, and a proactive approach to process improvements and safety compliance.

What are popular job titles related to Automation Supervisor jobs in Wisconsin? For Automation Supervisor jobs in Wisconsin, the most frequently searched job titles are:
What job categories do people searching Automation Supervisor jobs in Wisconsin look for? The top searched job categories for Automation Supervisor jobs in Wisconsin are:
Infographic showing various Automation Supervisor job openings in Wisconsin as of July 2026, with employment types broken down into 82% Full Time, 6% Part Time, 6% Contract, and 6% Nights. Highlights an 100% In-person job distribution, with an average salary of $117,698 per year, or $56.6 per hour.

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 14 days ago


Job description

Overview

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, NorthStar Medical Radioisotopes is the place to do it. NorthStar 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 NorthStar'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.

Position

The Automation Engineer will contribute to the development and execution of automation engineering tasks through design, planning, procurement, and execution, as well as coordinating with vendors and contractors. Some of these tasks include programming of PLC and HMI as well as associated documentation. Also included are assisting in the development and implementation of Manufacturing Execution Systems (MES) and associated networking and data management systems. This individual will be required to work with cross functional teams, including RA/QA and Process Engineering to apply efficient cGMP processes to preserve data integrity and the quality of the drug product, including the safety of all production and non-production personnel.

The Automation Engineer is responsible performing automation engineering tasks for the support of automated production systems at the Beloit campus. This includes the support of existing production system automation control software and hardware and transfer of automated equipment/systems and the associated control systems into production and providing the ongoing support of these systems to include standby support.  

The Automation Engineer will have responsibility to support actions and activities provided from senior engineering.

Responsibilities
  • 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,a nd project execution. 
Early Development

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.
Qualifications

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.

Shift Information

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%).

Benefits
  • 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
Working Conditions

This role may involve working in a controlled cleanroom environment, general office setting, or specific manufacturing areas. Conditions may include:

  • Exposure to varying temperatures, both indoors (heated/air-conditioned spaces) and outdoors
  • Noise levels range from quiet to loud, depending on the work area
  • Specific vision abilities, including near vision, visual acuity, and color discrimination

Personal Protective Equipment (PPE) is required and may include:

  • Respirators, gloves, safety glasses, and full protective clothing
  • Compliance with cleanroom gowning protocols (e.g., removal of all jewelry, including piercings)
  • Prohibition of cosmetics, fragrances (perfume, aftershave), and nail products, including polish, artificial nails, or extensions

As a radiopharmaceutical manufacturing site, radiation may be present in the laboratory and production areas. Employees in this role may be required to:

  • Follow strict radiation safety procedures
  • Participate in dosimetry monitoring and bioassay testing as part of the company protocol
  • Inform leadership of any health conditions that may affect product integrity, by cleanroom standards

In addition, all cosmetics, fragranced products (perfumes, aftershave, etc.), and nail products are prohibited, including clear nail polish, artificial nails, and nail extenders. 

The company is a radiopharmaceutical manufacturer and radiation may be present in manufacturing and laboratory areas. Employees may be required to be monitored using company provided dosimetry and bioassay testing.

Location

NorthStar Medical Radioisotopes is proud to call Beloit, Wisconsin home. Our headquarters and primary manufacturing facility are located in this vibrant, growing community that combines the charm of a small city with the advantages of a central Midwest location. Beloit features a lively, revitalized downtown filled with local restaurants, shops, and cultural events, and is just a short drive from major metropolitan areas including Madison, Milwaukee, Chicago, and Rockford.

Situated in the heart of the South Central Wisconsin and Northern Illinois region, Beloit offers a rare blend of urban amenities and scenic natural surroundings. Whether you're drawn to outdoor recreation, educational institutions, the arts, or historic landmarks, the area provides rich and diverse experiences for all interests. A variety of nearby communities, ranging from rural towns to suburban neighborhoods, offer flexible housing options and access to multiple school districts, making Beloit an excellent choice for individuals and families considering relocation.

NorthStar Medical Radioisotopes is an equal opportunity employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

Employment Type: FULL_TIME