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Posted 23 July, 2026

Principal Engineer,Pharma Recipe Authoring

Nagarro
Remote,India Full Time
Reference: 74_540894_744000116101017

Company Description

We're Nagarro.

We are a Digital Product Engineering company that is scaling in a big way! We build products, services, and experiences that inspire, excite, and delight. We work at scale across all devices and digital mediums, and our people exist everywhere in the world (17700+ experts across 39 countries, to be exact). Our work culture is dynamic and non-hierarchical. We're looking for great new colleagues. That's where you come in!

Job Description

REQUIREMENTS

Total experience 11+ years in Pharma Manufacturing / MES consulting
Hands-on experience with Pharma MES platforms such as Rockwell PharmaSuite, Siemens Pharma OpCenter, Werum PAS-X, or Tulip
Strong experience in Pharma Recipe Authoring and MBR/EBR/EMBR configuration and execution
Experience leading end-to-end MES implementations across Assessment, Design, Build, Integration, Validation, and Rollout phases
Strong understanding of GxP compliance, data integrity, audit trails, electronic signatures, and validation requirements
Experience with shopfloor system integration across ISA-95 layers (L1-L5) including automation, historians, and enterprise systems
Knowledge of ISA-95 and ISA-88 standards for manufacturing operations and recipe management
Experience working with multiple MES platforms with a platform-agnostic consulting mindset
Familiarity with manufacturing analytics platforms, historians, data lakes, or event streaming architectures
Experience working with global pharma manufacturing sites, multi-language deployments, and change management initiatives
Strong communication, collaboration, and stakeholder management skills across Operations, QA, IT, Automation, and Validation teams
Strong solutioning and pre-sales experience including customer workshops, opportunity shaping, and value articulation
Ability to translate business requirements into system design and technical solution architecture

RESPONSIBILITIES

Lead end-to-end MES implementation programs for pharmaceutical manufacturing environments
Conduct discovery workshops to identify business problems, define value cases, and shape MES opportunities
Drive process mapping (As-Is / To-Be), gap assessments, and requirements documentation (URS / FRS)
Design and configure Recipe Management, MBR/EBR workflows, exception handling, and Review-by-Exception processes
Architect and guide integration between MES, automation systems, ERP, LIMS, and other enterprise systems across L1-L5 layers
Lead cross-functional teams across functional design, system integration, validation, and deployment
Manage project scope, risks, milestones, and stakeholder communication across global programs
Ensure regulatory compliance alignment including GxP, audit trails, and electronic records/signatures
Support validation deliverables including documentation, testing coordination, and regulatory readiness
Provide solution leadership during pre-sales engagements including demonstrations, workshops, and proposal development
Influence customer decisions through value-based solutioning and risk-aligned architectural recommendations
Support global rollouts, hypercare support, and continuous improvement initiatives post-implementation

Qualifications

Bachelor's or master's degree in computer science, Information Technology, or a related fields

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