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$58.3K

$109.3K

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How much do syncade mes engineer jobs pay per year?

As of Aug 24, 2026, the average yearly pay for syncade mes engineer in Minnesota is $109,333.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,800.00 and $129,800.00 per year, depending on experience, location, and employer.

What is a Syncade MES Engineer?

A Syncade MES Engineer is responsible for implementing, configuring, and maintaining Emerson Syncade Manufacturing Execution System (MES) solutions in pharmaceutical, biotech, or manufacturing environments. They work to optimize production workflows, ensure system integration with other enterprise applications, and support process automation. Their role involves troubleshooting, validation, and compliance with industry regulations such as FDA 21 CFR Part 11. They collaborate with cross-functional teams to enhance operational efficiency and ensure seamless production execution.

What are the key skills and qualifications needed to thrive as a Syncade MES Engineer?

To thrive as a Syncade MES Engineer, you need a strong background in process automation, manufacturing execution systems (MES), and a degree in engineering or a related technical field. Proficiency with Emerson Syncade software, databases (SQL), and familiarity with industry standards such as GMP and 21 CFR Part 11 is highly valuable, as are certifications in automation or MES platforms. Strong troubleshooting, project management, and cross-functional communication skills help candidates excel in dynamic manufacturing environments. These competencies ensure successful MES deployments, ongoing system optimization, and seamless integration with broader production and IT teams.

What does a typical workday look like for a Syncade MES Engineer?

A typical workday for a Syncade MES Engineer involves configuring and maintaining the Emerson Syncade platform, collaborating with production teams to ensure smooth operation of manufacturing processes, and troubleshooting any system issues that arise. You’ll participate in project meetings, work closely with IT and automation departments, and write or update documentation to support GMP compliance. The role often includes supporting go-live activities for new functionality or upgrades and training end-users on best practices. This mix of hands-on technical work and cross-team collaboration provides variety and challenges, making every day different and engaging.

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Syncade Mes Engineer jobs near you

MES Consultant in Life Sciences - Intermediate to Principal

Enhanced Information Solutions

Stillwater, MN • Remote

Full-time

Re-posted 6 days ago

Job description

As a full-time MES consultant, you will provide consulting services to the biotech and pharmaceutical industries. You will work on project teams to assist with the implementation of manufacturing software and is expected to perform various roles in the software development life cycle, including programming, project management, software validation and unit testing. In addition, this role requires close interaction with clients and the ability to work and communicate with both team members and external stakeholders. When not at a client, the position provides the opportunity to perform development or validation activities for our OpsTrakker mobile app.

Project activities typically require a lot of personal interaction between EIS, vendors and our customers. Different projects typically require us to fill different roles, but there are three basic characteristics we are seeking: (1) very personable, (2) integrity/strong work ethic, (3) ability to quickly learn various skills. Additionally, we need people who have excellent communication skills, are great problem-solvers and can accurately analyze information to make proper decisions.

Occasional travel to customer sites is typically required. Frequency of travel varies greatly, depending on the project needs and the specific customer but likely will average 30-65%, when it is safe to travel.

EIS is a successful and very well-respected consulting company based in Stillwater, MN. With over 25 years in business, we are well positioned in a niche market within the pharmaceutical / biotech industries. Because demands for our services are rapidly increasing, we are entering an exciting period of growth, looking to add several resources.

Requirements:

  • Understanding of the software development life cycle and familiarity with the various phases such as gathering user requirements, developing software code and/or executing test protocol
  • Experience in Biotech/Pharmaceutical Manufacturing Systems required.
  • Bachelors degree in a relevant area such as Operations, Computer Science, Engineering, IT, or Business Administration
  • Authoring and/or Implementation experience with MES software packages such as POMS/POMSnet, PharmaSuite, Emerson Syncade, Korber PAS-X, OpsCenter, Tulip, Tempo, or other MES tool used in Life Sciences
  • Ability to travel to client sites when necessary.
  • Openness to career development and feedback to promote future job advancement.

Location: Remote within the United States, Puerto Rico, Ireland, France, Germany, and Trkiye. You must be authorized to work in one of these countries.

Travel: 30-65% based on client requirements

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