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, whilst 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.
Operating across 5 continents and with over 300,000 skilled employees, Cognizant partners with leading Life Sciences companies globally to provide performance improvements, reduced costs, and faster time to market. We are your end-to-end partner for consultancy, design, implementation, optimization, and support for all applications in the Pharmaceutical and Biotechnology Manufacturing stack.
We are seeking dedicated, innovative, and driven talent to join our expanding team.
Requirements
* Create business process flow diagrams for pharmaceutical product recipes based on paper batch records or source documents.
* Gather MES site-specific requirement analysis to develop URS and FRS.
* Logically break down recipes and manufacturing processes to configure recipes in Syncade.
* Develop/create MBR design elements (building blocks) and workflows in Syncade for repetitive use to expedite MBR creation.
* Gather master data and configure it in Syncade Development, Quality, and Production environments.
* Integrate Syncade with SAP and other automation systems using standard interface components of MBR design.
* Lead recipe design sessions with business process SMEs.
* Design MBR/recipe equipment workflows and status diagrams.
Responsibilities
* Develop, implement, and support MES recipes.
* Produce high-quality, well-documented, and maintainable configurations.
* Work with site teams to configure and support interfaces to other systems such as ERP, automation, and lab systems.
* Investigate and troubleshoot issues, providing solutions or recommendations for improvements.
* Implement system design changes following company quality standards and practices.
* Translate business requirements into design and perform testing of MES recipes and changes.
* Generate validation documentation in accordance with site procedures and GMP guidelines.
* Maintain a high level of integrity and quality in all work related to pharmaceutical production.
* Relate well to colleagues and stakeholders within and outside the MES team.
* The role may evolve to include out-of-hours support in the future.
Additional Details
* Seniority level: Entry level
* Employment type: Full-time
* Job function: Engineering and Information Technology
* Industries: IT Services, IT Consulting, Business Consulting and Services
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