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Protocol Intelligence
Data-driven signals on your job's competitivenessNiche MES and CSV expertise plus seniority limit qualified applicant density despite employer brand.
Requires pharma manufacturing MES and GxP validation experience, so background transferability is low.
Explicit 10+ years and mandatory MES (Körber/PAS‑X) plus CSV GxP experience create stringent shortlisting filters.
Job Description
Structured overview of role & requirementsAbout This Role
Translate manufacturing process requirements into global MES solutions and lead small to medium system enhancements.
Partner with global Manufacturing and Technology stakeholders on Manufacturing Execution, Material Flow, Shopfloor Control, Efficiency, and Track & Trace.
Ensure MES operational processes and GxP documentation are maintained and compliant.
Minimum Requirements
University degree in Computer Science, Management Information Systems, Engineering, or related discipline.
10+ years experience in process industry (preferably pharmaceutical manufacturing) within multinational environments.
5+ years experience in IT/OT project delivery and Computerized System Validation (CSV) in GxP-regulated environments.
Strong expertise in Manufacturing Execution Systems, specifically Körber/WERUM PAS-X, and understanding of Manufacturing IT ecosystems like OSI-PI, SAP PP/PI, SAP MII, warehouse systems, Track & Trace, and SCADA/Automation.
Ideal Candidate Profile
Experienced in delivering MES solutions in global pharmaceutical manufacturing settings with ability to handle complex stakeholder environments.
Proven ability to manage end-to-end system change delivery and drive continuous improvement within MES applications.
Able to influence senior stakeholders and communicate complex technical concepts clearly across organizational boundaries.