The Lead MES Designer owns the end-to-end design lifecycle for assigned workstreams, including blueprinting, PI configuration, and master data creation. They are responsible for facilitating show-and-tell sessions and defending design decisions to stakeholders such as Process Owners, QA, and Operations.
The MES Design Specialist provides independent review capacity and flex coverage across workstreams, including the execution of Design Review Checklists. They are responsible for identifying design errors, managing master data, and ensuring test case coverage for complex PI designs.
The Technical Project Manager is responsible for end-to-end delivery, including detailed schedule management, risk identification, and cross-workstream dependency oversight. They also manage validation documentation and ensure performance accountability within a complex multi-vendor governance structure.
The Business Change Manager manages the human side of system implementations by driving adoption planning and stakeholder alignment. They are responsible for owning the end-user training program and ensuring go-live readiness within a regulated pharmaceutical environment.
The role involves supporting pharmaceutical, medical device, and food manufacturing organizations through impactful projects in an agile environment. Responsibilities include solving complex equipment problems, creating concise technical documentation, and collaborating with plant operators.
