If you are an experienced MES engineer 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.
We are actively helping our customers to bring products to market with efficiency through accelerated product release through deviation management, process enforcement, ensuring record completion, and real-time equipment/material verification.
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 TECHNICAL CONSULTANT YOU WILL:
Proactively develop customer relationships; anticipate and provide solutions to customer needs giving high priority to customer satisfaction
Architect and lead the implementation of MES and system integration solutions projects
Conduct workshops to analyze user requirements to define functional requirements for MES solutions through client interviews and documentation analysis
Plan and organize the work of a project team, develop the implementation strategies for projects, act as a mentor for individuals within the group, and resolve issues within project teams while leading the team
Develop detailed designs, implement, troubleshoot and test Syncade MES solutions that meet client requirements
Refine/optimize and follow Business Process Maps and/or User Cases for configuration of execution workflows
Develop and improve processes, procedures and tools used in the execution of projects
Act as a liaison between the internal project team, internal management, sales and customer project teams and management
Understand the project scope and financials, and participate in the framing and quoting of projects to ensure successful project execution
Identify change orders and justify changes to Project Management; resolve issues and establish priorities between projects
Start-up complex systems at customers’ plants
WHO YOU ARE:
You achieve and are consistently known as a top performer.
You facilitate an open dialogue with a wide variety of contributors and stakeholders.
You deliver messages in a clear, compelling, and concise manner.
You continually scan the environment for technology breakthroughs.
REQUIRED EDUCATION, EXPERIENCE & SKILLS:
Bachelor of Science Minimum of 10+ years MES project experience, and at least 5 years’ experience working on MES projects in Biotech or Pharmaceutical manufacturing
MES project leadership and implementation experience including workflows, equipment management and materials management in Biotech or Pharmaceutical manufacturing
Recognized by others as a MES expert in Biotech or Pharmaceutical manufacturing
Must have the demonstrated ability to work in a team environment as both a leader and an individual contributor
Experience with SDLC (Waterfall/Agile)
Experience in at least one computer language in a regulated environment
Experience developing user requirements, Functional Specification documents and test scripts for MES projects.
Legal authorization to work in the United States
– sponsorship will not be provided for this position.
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:
ERP or Quality Systems integration a plus.
Knowledgeable in FDA validation requirements
Experience with regulatory/compliance documentation and procedures is a plus
Experience with .NET technologies