Nagarro

Pharma

AssociatePrincipalEngineer,PharmaReceiptAuthoring

India FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for not-applicable candidates.

The Brief

“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.

Pharma
Problems you'll solve

troubleshooting/resolution of complex MES and integration issues

Eligibility Requirements

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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