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Mes Software Engineer Jobs in Wisconsin (NOW HIRING)

$90K - $115K/yr

Control systems (PLCs, SCADA, MES integration) * Smart warehouse technology (WMS, WCS, IoT sensors ... Proficiency with automation design software (AutoCAD, SolidWorks, or similar) * Strong ...

Oversee the deployment and integration of Manufacturing Execution Systems (MES), Enterprise ... Manage IT infrastructure projects, including hardware, software, and networking solutions for ...

Showing results 41-60

Mes Software Engineer information

What are the key skills and qualifications needed to thrive as an MES software engineer, and why are they important?

To thrive as an MES Software Engineer, you need a strong background in computer science, programming (such as C#, Java, or Python), and manufacturing process knowledge, often supported by a relevant degree. Familiarity with Manufacturing Execution Systems (MES) platforms like Siemens Opcenter or Rockwell FactoryTalk, as well as database management and integration tools, is typically required. Analytical thinking, problem-solving, and effective communication are crucial soft skills for collaborating with cross-functional teams and addressing production challenges. Mastering these skills ensures efficient system implementation, smooth integration with manufacturing operations, and the delivery of reliable solutions that drive productivity.

What is an MES software engineer?

A MES (Manufacturing Execution System) Software Engineer is a professional responsible for designing, developing, implementing, and maintaining software systems that manage and control manufacturing operations on the shop floor. They bridge the gap between enterprise-level business systems (like ERP) and real-time production processes, ensuring data flows smoothly and efficiently. MES Software Engineers work with technologies such as databases, PLCs, and industrial automation systems to optimize manufacturing performance, improve quality, and enable traceability. Their role often involves collaborating with production teams, IT professionals, and equipment vendors to deliver tailored MES solutions.

What are some common challenges faced by MES software engineers when integrating new manufacturing technologies?

MES Software Engineers often encounter challenges when integrating new manufacturing technologies, such as ensuring seamless data flow between legacy and modern systems, adapting to diverse machine protocols, and maintaining system reliability during upgrades. Collaboration with production and IT teams is essential to address compatibility and minimize downtime. Staying up-to-date with evolving industry standards and cybersecurity best practices is also a key part of the role.

What is the difference between Mes Software Engineer vs Manufacturing Software Engineer?

AspectMes Software EngineerManufacturing Software Engineer
Required CredentialsBachelor's in Software Engineering, Computer Science, or related field; familiarity with MES systemsBachelor's in Software Engineering, Computer Science, or related field; experience with manufacturing processes
Work EnvironmentIndustrial settings, manufacturing plants, office environmentsFactories, production lines, office settings
Employer & Industry UsageManufacturing companies implementing MES solutionsManufacturing firms focusing on production software
Common Search & ComparisonYesYes

The Mes Software Engineer primarily focuses on developing and maintaining Manufacturing Execution System (MES) software to optimize production processes. Manufacturing Software Engineers may work on broader manufacturing software solutions, including MES but also other systems like ERP or automation tools. While both roles require similar technical skills and often overlap in manufacturing environments, Mes Software Engineers specialize specifically in MES platforms, making them more targeted for companies implementing MES solutions.

What are popular job titles related to Mes Software Engineer jobs in Wisconsin? For Mes Software Engineer jobs in Wisconsin, the most frequently searched job titles are:
What job categories do people searching Mes Software Engineer jobs in Wisconsin look for? The top searched job categories for Mes Software Engineer jobs in Wisconsin are:
Infographic showing various Mes Software Engineer job openings in Wisconsin as of August 2026, with employment types broken down into 84% Full Time, and 16% Contract. Highlights an 84% In-person, 11% Hybrid, and 5% Remote job distribution.

Automation Engineer II

NorthStar Medical Radioisotopes

Beloit, WI โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 18 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 II 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 II 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 some standby support.

The Automation Engineer II will have responsibility on a project level from conception to final commissioning and validation.

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%).

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 and document 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.
  • Provide automation technical knowledge for troubleshooting, investigations and training associated with Automation software as well as integrated automation system related hardware including sensors, valves, pneumatics, conveyors, robotics, vision systems, filling systems, automatic packaging equipment, etc.
  • Support the validation of automation systems per cGMP and Regulatory guidance.
  • Provide automation system design in relation to data acquisition, integrity and retention, required for system tracking and trending, including development of data interfaces between disparate systems to include 21CFR Part 11 and Annex 11.
  • 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.
  • Understand and interpret P&ID drawings, electrical schematics and wiring diagrams; PLC based logic and system integration (Siemens TIA preferred); and NFPA, UL, CE, NEC requirements.
  • Continuously adapt to an ever-changing regulatory environment such that the Company is in compliance with current regulations.
  • Develop and strengthen team capabilities through mentoring, training, and technical oversight of less experienced engineers.
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 ensure timely delivery of radiopharmaceuticals for cancer treatment.
  • Gain hands-on experience with automation technology under the guidance of industry experts.
  • After 6 months, you will:

  • Develop advanced technical skills in handling automated processes and technologies, positioning yourself as a key player in an innovative and impactful field.
  • Troubleshoot various automation systems.
  • Implement automation changes to existing control system hardware and software, supervise hardware and software modifications done by outside vendors, and develop specification and test documentation.
  • Qualifications

    Bachelor's degree in Engineering and minimum three (3) years of experience with a concentration in Automation or Process Control; or combination of education and experience. Knowledge of automation hardware design and maintenance required.ย  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.ย  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.ย  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.ย 

    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