We are seeking a MES Engineer to design, build, validate, and troubleshoot MES recipes in support of Make/Assess/Release in a 24x7 Goods Manufacturing Practice (GMP) environment. The ideal candidate will have experience with Manufacturing Execution Systems (MES) and be able to contribute to Manufacturing Operations Management initiatives and optimization/standardization of the global IT OT landscape.
Requirements
- Manufacturing Execution System (MES) Rockwell (PharmaSuite) recipe authoring and software development
- Troubleshooting plant floor MES execution and business system integration issues
- Compliance with corporate and site business processes, valid design principles, and quality procedures
- Qualification test plan development/review/approval and execution
- Implementing production tech transfer requirements into automation IT systems
- Contributing to development of solutions for reporting, production and operational analysis tools, recipe procedural enhancements, batch review/release, equipment automation integration, and business system integration
- Update and maintain Standard operating procedures associated with the MES systems and processes
- Present system and electronic batch record process to health authorities
- Contributing to development of supply chain network MES standards and best practices
- Provide Consulting with Business Process owners in the Value Streams
- Contribute with MES Recipe Authoring knowledge to Projects/Squads for MES Projects, process improvement initiatives or support
- Troubleshoot immediate system issues, and inquiries as they arrive during normal business hours.
- Participate in an after hours on-call support rotation
- Document system changes and incidents in ServiceNow
- Own and manage Change records and Deviation in Veeva Quality System
Benefits
- Generous Paid Time Off
- 401k Matching
- Retirement Plan
- Discretionary annual bonus