Cognizant Life Science Manufacturing Group (LSMG) operates 100% in Life Sciences. We are world leaders in delivering superior software solutions that facilitate better patient outcomes. We are focused on improving our customers’ performance across the manufacturing enterprise through the application of innovative technologies. LSMG is a partner to numerous world leading Life Science multinational companies where we continue to deliver value to their manufacturing operations.
Position: MES Engineer Syncade
Location: Dublin, Ireland
Duration: Fulltime
About the role:
We are currently looking to hire Senior MES Engineers (Syncade) to join our Ireland MES Projects Team, supporting multiple projects with the worlds leading Pharmaceutical and Biotech companies.
Responsibilities:
* Create business process flow diagram for pharmaceutical product recipes based on the paper batch record or source documents.
* Gather MES Site specific requirement analysis to develop URS and FRS.
* Logically breakdown the recipes/Mfg. process to configure the recipe in to Syncade
* Develop/create MBR design elements (building blocks) and workflows in Syncade for repetitive use in MBR creation to expedite the process.
* Gather master data and configure in Syncade Development/Quality/Production Environment.
* Integrating Syncade with SAP and other automation systems using standard interface component of MBR design.
* Lead the recipe design session with business process SMEs.
* Design MBR/recipe, equipment workflow/ status diagram based on the Business process flow.
* Create solution design and configuration document.
* Prepare key user training documents and impart key user training.
* Provide assistance in business SOP creation.
Requirements:
* A Bachelor’s degree in Computer Science, Computer Engineering, Computer Information Systems, or a related field (Technology Management; Chemical Engineering)
* Senior level Syncade experience desired
* Total 5+ years of hands-on experience on MES Product, Min 2+ years in MBR designing role.
* Syncade product hands-on experience for Full application configurations including interface with SAP and automation systems.
* In-depth of knowledge of Bio Pharma processes
* Creation of business process flow diagram
* Master Batch Record creation in Syncade
* Knowledge on Industry Standards S88 and ISA S95
* Pharmaceutical validation concept
* cGMP and GDP standards and GAMP Standards
* Good verbal, written communication