Cognizant is a world leader in delivering digital transformation solutions to Life Sciences. Through our knowledge and expertise in Automation, MES & Digital, we deliver stable manufacturing systems that are optimized to improve operational efficiencies while maintaining compliance. Our specialist engineering teams have the aptitude to deliver and support Pharma 4.0 architectures and solutions covering all IT, OT, and IoT applications, infrastructures, and services.
Job Summary: Create business process flow diagrams 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 break down the recipes/mfg. process to configure the recipe into Werum PAS-X. Develop/create MBR design elements (building blocks) and workflows in Werum PAS-X for repetitive use in MBR creation to expedite the process. Gather master data and configure it in Werum PAS-X Development/Quality/Production. Roles & Responsibilities: Integrate Werum PAS-X with SAP and other automation systems using standard interface components 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 documents. Prepare key user training documents and impart key user training. Aid in business SOP creation. The Ideal Candidate: A Bachelor's degree in Computer Science, Computer Engineering, Computer Information Systems, or a related field (Technology Management; Chemical Engineering). Senior level Werum PAS-X experience desired. Total 5+ years of hands-on experience with MES Products. Werum PAS-X product hands-on experience for full application configurations including interface with SAP and automation systems. In-depth knowledge of Bio Pharma processes. Experience in the creation of business process flow diagrams. Master Batch Record creation in Werum PAS-X. Knowledge of industry standards S88 and ISA S95. Understanding of pharmaceutical validation concepts. Familiarity with cGMP, GDP standards, and GAMP standards.
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