OverviewCognizant 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 the leading Life Sciences companies globally to provide performance improvements, reduced costs and improve time to market. We are your single end to end partner for consultancy, design implementation, optimization and support for all applications in the Pharmaceutical and Biotechnology Manufacturing stack.We're looking for dedicated, innovative and driven talent to join our expanding team.ResponsibilitiesProactively resolving technical issues before they impact the business priorities and operationalAutomation support requestsOn-floor support of manufacturing activities. DCS interface to Syncade MES.Support the smooth running of the site value stream and supply by providing and being part of the AIT Automation Delta V Shift support team.Ensure supply of high-quality product through ensuring equipment and system availability maximize performance through continuous process improvement initiatives and other relevant operational support requirementsEnsure adherence implementation and execution of local SOPs and technical documentation e.g., Change Management Execution Incident Problem Management Quality Notifications SDLC documentationRequired to comply with company Global Policies Procedures and Guidelines regulatory requirements and execute current good manufacturing Practices (cGMP) and SDLC/CSV in the performance of day-to-day activities and all applicable job functionsWhile Delta V Shift support is the primary focus support and troubleshooting of supporting PLC/HMI and Scada based systems will be required.Work collaboratively to drive a safe and compliant culture in Company.May be required to perform other duties as assigned3 Year Automation Experience in a GMP environment ·Job DetailsSeniority level: AssociateEmployment type: Full-timeJob function: Information Technology and ManufacturingIndustry: Pharmaceutical Manufacturing
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