Principal Engineer,Pharma Recipe Authoring
Nagarro · Remote, IN
Publiée le 23 mars 2026
Postuler Ă cette offre avec Jobrona
Créez votre compte et importez votre CV. Si cette offre lui correspond, nous préparons et envoyons d'abord cette candidature et vous montrons exactement ce qui a été envoyé.
Ă propos du poste
đđŒWe'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!
REQUIREMENTS
âą Total experience 11+ years in Pharma Manufacturing / MES consulting
âą Hands-on experience with Pharma MES platforms such as Rockwell PharmaSuite, Siemens Pharma OpCenter, Werum PAS-X, or Tulip
âą Strong experience in Pharma Recipe Authoring and MBR/EBR/EMBR configuration and execution
âą Experience leading end-to-end MES implementations across Assessment, Design, Build, Integration, Validation, and Rollout phases
âą Strong understanding of GxP compliance, data integrity, audit trails, electronic signatures, and validation requirements
âą Experience with shopfloor system integration across ISA-95 layers (L1âL5) including automation, historians, and enterprise systems
âą Knowledge of ISA-95 and ISA-88 standards for manufacturing operations and recipe management
âą Experience working with multiple MES platforms with a platform-agnostic consulting mindset
âą Familiarity with manufacturing analytics platforms, historians, data lakes, or event streaming architectures
âą Experience working with global pharma manufacturing sites, multi-language deployments, and change management initiatives
âą Strong communication, collaboration, and stakeholder management skills across Operations, QA, IT, Automation, and Validation teams
âą Strong solutioning and pre-sales experience including customer workshops, opportunity shaping, and value articulation
âą Ability to translate business requirements into system design and technical solution architecture
RESPONSIBILITIES
âą Lead end-to-end MES implementation programs for pharmaceutical manufacturing environments
âą Conduct discovery workshops to identify business problems, define value cases, and shape MES opportunities
âą Drive process mapping (As-Is / To-Be), gap assessments, and requirements documentation (URS / FRS)
âą Design and configure Recipe Management, MBR/EBR workflows, exception handling, and Review-by-Exception processes
âą Architect and guide integration between MES, automation systems, ERP, LIMS, and other enterprise systems across L1âL5 layers
âą Lead cross-functional teams across functional design, system integration, validation, and deployment
âą Manage project scope, risks, milestones, and stakeholder communication across global programs
âą Ensure regulatory compliance alignment including GxP, audit trails, and electronic records/signatures
âą Support validation deliverables including documentation, testing coordination, and regulatory readiness
âą Provide solution leadership during pre-sales engagements including demonstrations, workshops, and proposal development
âą Influence customer decisions through value-based solutioning and risk-aligned architectural recommendations
âą Support global rollouts, hypercare support, and continuous improvement initiatives post-implementation
Bachelorâs or masterâs degree in computer science, Information Technology, or a related fields