Skillset: Emerson – Syncade MES
Experience : 3-11 years' experience profiles
- Must have experience in pharma domain more than 3+ years
- Having experience on Emerson Syncade Installation Qualification, Upgrade, Development and Configuration.
- Design, implementation, validation & support of MES solution for MES projects based on Emerson MES platform- Syncade as per standard methodologies (using ASP.Net, C#, MVC, SQL, VB Script and VB.Net) on Lifesciences Projects.
- Develop Webpart, Batch Reports and Integration with L2, L3 and L4 systems (e.g. ERP integrations- Oracle EBS, SAP, LIMS, CMMS etc)
- Develop and execute validation protocols for MES implementations, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
- Configure Syncade workflows, electronic batch records, data interface and other MES functionalities to meet client specifications and enhance process efficiency.
- Provide technical expertise and support to clients during MES system upgrades, expansions, and troubleshooting activities.
- Collaborate with project managers and cross-functional teams to ensure alignment of MES implementation and validation activities with project timelines and objectives.
- Stay current with industry trends, regulatory guidelines, and advancements in MES technology to continuously improve implementation and validation processes.
- Implement system design changes in accordance with company Quality Standards and Practices
- Strong understanding of manufacturing processes and regulatory requirements (e.g., FDA regulations, GAMP 5) related to MES implementations.
- Work closely with business management and users to strategically define the needs and design solutions that add value
- Create and maintain required documentation for the project execution.