We're looking for a Principal Engineer,Pharma Recipe Authoring to lead end-to-end MES implementation programs for pharmaceutical manufacturing environments and ensure regulatory compliance alignment.
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
