Serialization Validation Specialist / Engineer
W skrócie
Validation Specialist for pharmaceutical serialization systems. Responsibilities include test case design/execution, integration validation (ERP, WMS, packaging lines), and documentation. EU-based, travel to France/Belgium required. Project until end of 2026.
Słowa kluczowe
Skrót przygotowany przez AI na podstawie treści ogłoszenia.
We are looking for an experienced Validation / Testing Specialist to support a pharmaceutical manufacturing project focused on the validation of serialization processes and their integration across packaging lines, ERP, warehouse management, and manufacturing IT systems.
The project includes on-site line testing in France or Belgium, therefore the successful candidate must be based within the EU and available for travel to the project site. The validation activities are planned to be completed by the end of 2026.
Key Responsibilities
Design, prepare, and execute Functional, System Integration, User Acceptance, and Regression Test Cases.
Validate serialization hierarchy and aggregation processes, including Unit → Case → Pallet.
Perform end-to-end verification of serialization transactions across:
Packaging line equipmentERP systems
Warehouse Management SystemsL4/L5 manufacturing and serialization systems
Test and validate integrations between:
SAP ATTPSAP ECC / S/4HANAWarehouse Management Systems (WMS)
Packaging line equipment
Perform manual testing directly on production/packaging lines and support on-site validation activities.
Investigate, document, and follow up on defects and testing issues.
Maintain complete validation documentation, test evidence, execution records, and traceability in accordance with project and quality requirements.
Collaborate closely with IT, automation, manufacturing, QA, and business stakeholders to ensure successful validation and system readiness.
| Opublikowana | 2026-08-31 |
| Wygasa | 2026-11-29 |
| Źródło |
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