Nagarro
Pharma
AssociatePrincipalEngineer,PharmaReceiptAuthoring
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“Associate Principal Engineer, Pharma Receipt Authoring at Nagarro. Skills: Pharma MES platforms, MES implementation, Recipe Authoring, shopfloor integration, GxP compliance. Lead end-to-end Pharma MES implementation programs across the complete project lifecycle. Conduct discovery workshops, understand customer manufacturing processes, and define target operating models”
Industry & Context.
troubleshooting/resolution of complex MES and integration issues
Flexible to travel for domestic and international customer workshops as required, Ability to lead customer workshops, solution discussions, and pre-sales engagements, Participate in customer presentations, solutioning discussions, and pre-sales activities to shape opportunities and influence decisions
What They're Looking For.
Must Have
Total experience 12+ years, Experience in Pharma Manufacturing / MES consulting, hands-on experience in Pharma MES platforms such as Rockwell PharmaSuite, Siemens Opcenter, PAS-X, or Tulip, Expertise in Pharma Recipe Authoring, MBR/EBRBR setup, execution workflows, exception handling, review-by-exception, and e-signatures, understanding of Pharma 4. 0 concepts, ISA-95 / ISA-88 standards, and shopfloor digitalization, Experience in end-to-end MES implementations including Assessment, Design, Build/Configuration, Integration, Validation, Rollout, and Hypercare, Proven experience in shopfloor integration across L1 to L5 systems, including historians, automation systems, ERP, and enterprise applications, experience in process mapping (As-Is / To-Be), gap assessment, URS/FRS preparation, and solution blueprinting, Experience in compliance-driven environments with knowledge of GxP, data integrity, audit trails, validation, and electronic signatures, stakeholder management skills working with Operations, QA, IT, Automation, and Validation teams, Experience leading global MES rollouts across multiple manufacturing sites and managing multilingual deployments, Excellent communication, collaboration, presentation, and customer-facing consulting skills, Ability to lead customer workshops, solution discussions, and pre-sales engagements
Nice to Have
Exposure to manufacturing analytics, cloud/data platforms, historians, event streams, and data lakes is preferred
What You'll Do.
Lead end-to-end Pharma MES implementation programs across the complete project lifecycle
Conduct discovery workshops
understand customer manufacturing processes
and define target operating models
Translate business and shopfloor requirements into MES functional and technical solution designs
Lead recipe authoring activities including MBR/EBR configuration
and review-by-exception processes
Drive process mapping
URS/FRS documentation
and solution blueprint preparation
Architect and guide integrations between MES
and enterprise platforms across L1-L5 layers
Ensure compliance alignment with GxP
validation requirements
and data integrity standards
Lead workstreams and mentor teams across functional
and validation tracks
stakeholder communication
and delivery governance
and hypercare activities
Provide strategic recommendations and solution trade-offs aligned with customer value
and compliance objectives
Drive continuous improvement initiatives
How You'll Work.
Team & Collaboration
Collaborate with cross-functional teams including QA, Manufacturing Operations, Validation, IT, and Automation stakeholders; Mentor teams across functional, integration, and validation tracks
Communication Scope
Excellent communication; presentation; customer-facing consulting skills; stakeholder communication
Process & Methodology
Manage project scope, risks, milestones, estimations, stakeholder communication, and delivery governance, Lead end-to-end Pharma MES implementation programs
Full Job Description
* Total experience 12+ years * Experience in Pharma Manufacturing / MES consulting. * Strong hands-on experience in Pharma MES platforms such as Rockwell PharmaSuite, Siemens Opcenter, PAS-X, or Tulip. * Expertise in Pharma Recipe Authoring, MBR/EBR/EMBR setup, execution workflows, exception handling, review-by-exception, and e-signatures. * Strong understanding of Pharma 4.0 concepts, ISA-95 / ISA-88 standards, and shopfloor digitalization. * Experience in end-to-end MES implementations including Assessment, Design, Build/Configuration, Integration, Validation, Rollout, and Hypercare. * Proven experience in shopfloor integration across L1 to L5 systems, including historians, automation systems, ERP, and enterprise applications. * Strong experience in process mapping (As-Is / To-Be), gap assessment, URS/FRS preparation, and solution blueprinting. * Experience in compliance-driven environments with knowledge of GxP, data integrity, audit trails, validation, and electronic signatures. * Strong stakeholder management skills working with Operations, QA, IT, Automation, and Validation teams. * Experience leading global MES rollouts across multiple manufacturing sites and managing multilingual deployments. * Exposure to manufacturing analytics, cloud/data platforms, historians, event streams, and data lakes is preferred. * Excellent communication, collaboration, presentation, and customer-facing consulting skills. * Ability to lead customer workshops, solution discussions, and pre-sales engagements. * Flexible to travel for domestic and international customer workshops as required. RESPONSIBILITIES: * Lead end-to-end Pharma MES implementation programs across the complete project lifecycle. * Conduct discovery workshops, understand customer manufacturing processes, and define target operating models. * Translate business and shopfloor requirements into MES functional and technical solution designs. * Lead recipe authoring activities including MBR/EBR configuration, executi
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