Live opening · Posted 3 days ago
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About the role
Description supplied by the original job listing.
We are seeking an experienced PAS-X Solution Consultant / Subject Matter Expert (SME) to support a global MES template rollout across multiple pharmaceutical manufacturing sites. This individual will play a key role in PAS-X solution design, integration, process standardization, testing, and deployment within a regulated GxP environment.
The successful candidate will bring strong expertise in Werum PAS-X, pharmaceutical manufacturing processes, SAP integration, and Electronic Batch Record (EBR) solutions.
Key Responsibilities
Act as the PAS-X SME across global manufacturing programs.
Support the design, implementation, and rollout of a global PAS-X template solution.
Collaborate with business stakeholders, manufacturing teams, and technical partners to standardize and optimize manufacturing processes.
Support process design activities using ARIS and testing activities using HP ALM.
Contribute to end-to-end testing, validation, deployment, and hypercare activities.
Ensure alignment with global manufacturing standards and governance frameworks.
Required Experience
PAS-X Functional Expertise
Strong hands-on experience with Werum PAS-X, including:
Weighing & Dispensing
Material Flow
Label Management
Master Data Management
SAP-integrated master data
Custom Attributes (CA) and Characteristics (CX)
Production Unit Maintenance
Exception Management
Rights & Roles
Electronic Signatures and Workflows
Master Batch Record (MBR) Design
Formula Design
Generic MBR (gMBR) / PVL concepts
In-Process Control (IPC)
Electronic Batch Records (EBR)
Equipment Management
State Diagrams
Machine Integration
Batch Record Review (BRR)
Integration Experience
Strong experience integrating PAS-X with SAP WM and/or SAP EWM.
Experience with PAS-X MSI and PAS-X APIs.
Ability to create and manage orders, materials, and master data to support end-to-end testing activities.
Reporting & Analytics
Experience with PAS-X reporting solutions and data extraction capabilities.
Knowledge of PAS-X PDA (Product Data Access).
Experience supporting data exports to enterprise reporting platforms and data lakes.
Familiarity with Power BI.
Experience with Crystal Reports and/or Jaspersoft is highly desirable.
Industry Experience
Pharmaceutical, Biotechnology, or Life Sciences industry background.
Strong understanding of:
ISA-95
GxP
Computer System Validation (CSV)
Preferred Qualifications
Experience supporting global template deployments and multi-site rollouts.
Strong communication and stakeholder management skills.
Ability to work effectively with global cross-functional teams.
Experience within large-scale digital manufacturing transformation programs.
Exposure to manufacturing operations across multiple international sites.
Employment type
Full-time
Work arrangement
Hybrid
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