Principal Engineer,Pharma Receipt Authoring

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 (L1L5) 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 L1L5 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 :

Bachelors or masters degree in computer science Information Technology or a related fields

Remote Work :

Yes

Employment Type :

Full-time