Associate Staff Engineer,Siemens OpCenter at Nagarro1

REQUIREMENTS • Total experience: 4+ years • Strong experience in Siemens OpCenter Pharma (MES) with end-to-end implementations • Mandatory experience in Recipe Authoring / MBR (Manufacturing Batch Record) design • Good understanding of ISA S88 standards and batch process modeling • Experience in designing operations, unit procedures, and recipes aligned with MBR • Strong knowledge of pharmaceutical/biotech manufacturing processes • Hands-on experience with Electronic Batch Records (EBR) design and validation • Experience with GxP systems, CSV (Computer System Validation), and SDLC methodologies • Good understanding of 21 CFR Part 11 compliance and regulatory requirements • Exposure to quality and manufacturing impacts in MES implementations • Knowledge of MOM platform and integration capabilities • Experience in process development and manufacturing execution in pharma/biotech domain • Strong stakeholder management and ability to work with cross-functional teams • Experience in leading teams or handling complex project deliveriesRESPONSIBILITIES • Lead Siemens OpCenter MES solution design and implementation • Analyze business process flows and translate them into MES recipes and workflows • Design and develop recipes, operations, and unit procedures aligned with S88 and MBR • Collaborate with business and manufacturing teams to ensure process alignment and compliance • Drive EBR design, configuration, and validation activities • Ensure compliance with GxP, 21 CFR Part 11, and validation standards (CSV) • Conduct requirement workshops and convert them into functional and technical MES designs • Support UAT, system validation, and production deployment activities • Identify and manage quality and manufacturing risks during MES implementation • Work on integration of MES with upstream/downstream systems • Provide technical leadership, mentoring, and governance for MES projects • Drive continuous improvements and innovation within MES/MOM landscape