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# Single Use Systems (SUS) Engineer _ Life Science

- **Company:** Capgemini
- **Location:** Diegem (Machelen), Belgium
- **Contract:** Permanent contract
- **Skills:** Databases, Data Integrity, Document Management Systems, Data Management, GXP
- **Published:** July 10, 2026
- **Apply:** https://www.capgemini.com/jobs/516047-fr_FR_SAPBTP/x/

## About the Role

* Bachelor's degree or higher in Engineering, Biotechnology, Life Sciences, Pharmaceutical Sciences, Industrial Operations, or related field.
 * Experience in a pharmaceutical, biotechnology, medical device, or other regulated manufacturing environment.
 * Strong data management and documentation skills.
 * Ability to analyze technical information and maintain structured databases.
 * Knowledge of GMP/GxP environments is highly desirable.
 * Familiarity with validation processes, quality systems, or manufacturing operations is a plus.
 * Excellent communication and stakeholder management skills.
 * Ability to work with technical specifications and engineering documentation.
 * Experience with ERP, MES, Quality Management Systems, or document management platforms is an advantage.
 * Comprehensive SUS inventory and database.Accurate and up-to-date technical documentation repository.Improved traceability of single-use components.Support for compliance, audit readiness, and validation activities.Standardized data management practices across manufacturing operations.
 * French: Fluent
 * English: Professional working proficiency.

## Description

As part of the MPU Validation Platform supporting vaccine manufacturing operations, the consultant will be responsible for developing, maintaining, and optimizing a comprehensive database covering all Single Use Systems (SUS) utilized across manufacturing processes. This role will support traceability, compliance, standardization, and continuous improvement initiatives within a highly regulated pharmaceutical environment., * Identify and map Single Use Systems (SUS) and components used across manufacturing units.

 * Collect, verify, and consolidate technical documentation related to SUS assemblies and materials.
 * Build and maintain a structured and reliable database containing:
 + Component specifications
 + Supplier information
 + Bills of Materials (BOM)
 + Certificates of Compliance (CoC)
 + Material and validation data
 * Ensure data integrity, accuracy, and consistency across all records.
 * Collaborate with Validation, Quality Assurance, Manufacturing, Engineering, and Process teams to gather and validate information.
 * Support change control, risk assessment, and regulatory compliance activities through accurate data management.
 * Contribute to standardization initiatives across manufacturing sites and processes.
 * Generate reports and dashboards to support operational and quality decision-making.
 * Participate in continuous improvement projects related to SUS lifecycle management.


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