Overview
On Site
Depends on Experience
Contract - W2
Contract - Independent
Contract - 12 Month(s)
Skills
MES
Manufacturing Execution Systems
MES Recipe Development
Troubleshooting
Werum PAS-X
Syncade
FactoryTalk
Opcenter
GxP
FDA
21 CFR Part 11 Compliance
SQL
System Integration
Validation
Integration Testing
Manufacturing
Development Testing
Documentation
Enterprise Resource Planning
Estimating
Collaboration
Communication
Computerized System Validation
Data Flow
Database
Scripting
Siemens
Software Design
Systems Design
Training
User Guides
Pharmaceutics
Programmable Logic Controller
Regulatory Compliance
SCADA
GMP
Manufacturing Execution System
Manufacturing Operations
Medical Devices
SAP
Workflow
Job Details
We are seeking a Manufacturing Execution Systems (MES) Engineer to join our client s global manufacturing technology team based in Dublin, Ohio. The ideal candidate will be responsible for solutioning, documentation, administration, deployment, and maintenance of MES environments across global production sites.
You will collaborate with cross-functional teams including Manufacturing, Technology, Engineering, and Quality to ensure seamless integration, support, and enhancement of MES applications critical to manufacturing operations.Key Responsibilities:
You will collaborate with cross-functional teams including Manufacturing, Technology, Engineering, and Quality to ensure seamless integration, support, and enhancement of MES applications critical to manufacturing operations.Key Responsibilities:
- Provide MES solution design, configuration, and deployment support for development, test, and production environments.
- Collaborate with site functional teams to gather user requirements and convert them into system and process specifications.
- Support and troubleshoot MES recipes, workflows, and application components that support day-to-day manufacturing operations.
- Track and resolve technical issues and customer complaints, coordinating with vendors as needed.
- Develop and maintain user guides, training resources, and documentation for MES users and stakeholders.
- Lead and execute manual unit and integration testing, ensuring quality and compliance.
- Conduct peer reviews of system design and source code, providing actionable feedback.
- Deliver accurate effort estimates, project updates, and adhere to deadlines in a dynamic work environment.
- Ensure all work complies with industry regulations, GMP standards, and internal quality guidelines.
- 5+ years of hands-on experience with Manufacturing Execution Systems (MES), preferably in a regulated industry (pharma, biotech, medical devices, or automotive).
- Strong knowledge of MES configuration, deployment, and integration with enterprise systems.
- Experience with troubleshooting MES recipes, process workflows, and production data flows.
- Familiarity with SQL databases, scripting, and automation for MES administration.
- Proven ability to translate business requirements into technical solutions.
- Excellent documentation, communication, and cross-functional collaboration skills.
- Understanding of GxP, FDA, or other regulatory frameworks for manufacturing systems.
- Experience with MES tools such as Werum PAS-X, Rockwell FactoryTalk PharmaSuite, Siemens Opcenter, or Emerson Syncade.
- Exposure to automation systems (PLC/SCADA), ERP integration (SAP), and data historians.
- Background in Computer Systems Validation (CSV) and 21 CFR Part 11 compliance.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.