MES Engineer - Intermediate

MES Intermediate Engineer/Technologist
If you are an experienced MES professional looking to work with a team of MES specialists at some of the most innovative pharma manufacturing companies in the world, this position should interest you. Our Emerson Life Science global team of MES engineers currently work on projects for customers involving Cell and Gene therapies, chemical synthesis, biopharma, and other Life Science areas.
“Hi, I’m Steve Murray, and I manage the MES Projects team in North America. Our team works with many of the leading pharma/biopharma manufacturers in the world to drive efficiency and the development of solutions that helps get critical therapies and life-saving products to market including vaccines, cancer treatments, and other therapeutics (including many for COVID). We welcome innovative minds to join our team as we strive to continue to deliver innovations to the market to help our customers efficiently make cutting-edge therapeutics available to the world.”
Our teams also deliver high value system integrations to ERP, LIMS, CMMS, and control systems – including Emerson’s own, industry-leading, DeltaV DCS, as we deliver value with our Syncade MES platform.

AS AN MES INTERMEDIATE ENGINEER / TECHNOLOGIST YOU WILL:

• Work with customers to analyze/develop functional requirements for MES solutions through client interviews and documentation analysis
• Work in a team to develop detailed designs, implement, troubleshoot and test Syncade MES solutions that meet client/project requirements
• Quickly learn new skills and technologies
• Start-up complex systems at customers’ sites
• Proactively develop customer relationships; anticipate and provide solutions to customer needs giving high priority to customer satisfaction

WHO YOU ARE:
You persist in accomplishing objectives despite obstacles and setbacks. You partner with others to get work done. You adjust communication to fit the audience and the message. You follow through on commitments.

REQUIRED EDUCATION, EXPERIENCE & SKILLS:

• BS in Engineering with a minimum of 3 years experience with more than 1 year experience working with a MES system in the process or medical device industry or a 2 or 4 year degree/diploma with a minimum of 4 years of experience working with MES in the process or medical device industry
• Demonstrated interest in software development
• A minimum of 25% travel is expected with this position. Travel will be mostly domestic, but some international travel may be required

PREFERRED EDUCATION, EXPERIENCE & SKILLS:

• 3 years process operations experience in a highly automated pharmaceutical, biotechnology, or similar regulated manufacturing facility subject to Good Manufacturing Practices (GMP) regulations.
• Syncade and/or Deployment experience with plant floor/Manufacturing Execution Systems (MES) solutions (e.g. Syncade, Rockwell ProPack Data, Werum PAS-X)
• Knowledgeable in FDA validation requirements preferred, including: User Requirement and Design Specs, Business Process Procedures, Design Reviews, Requirements gathering
• Experience with .NET technologies
• Experience working with customers to create user requirements/functional specifications, test scripts