Principal Engineer, Pharma Recipe Authoring

Job not on LinkedIn

🕒 March 23

🇮🇳 India – Remote

⏰ Full Time

🔴 Lead

🧑‍💻 Full-stack Engineer

👻 Ghost score 45%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Nagarro

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1996

💼 Consulting

📣 Marketing

🏥 Healthcare

Consulting • Marketing • Healthcare

Nagarro is a global leader in digital engineering and technology consulting. The company helps clients become innovative, digital-first businesses by leveraging technology to drive business breakthroughs. Known for its entrepreneurial agility and CARING mindset, Nagarro offers a wide range of services, including digital engineering, intelligent enterprise solutions, and experience and design services. With over 17,900 employees across 37 countries, Nagarro collaborates with industry leaders to accelerate digitalization and technology-led innovation.

📋 Description

• 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

🎯 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.

🏖️ Benefits

• Employees can work remotely