System Quality Assurance Consultant - ERP Validation (M/F)

Joining Meent means?

Joining an expert engineering company in Life Science, created in 2023, which values the talent and energy of its employees to carry out innovative and ambitious projects.

At Meent Life Science, we build an adventure with our employees based on:

• Mutual aid and team spirit
• Benevolence and stability
• Fulfillment and professional progression

We believe that a fulfilled employee is a high-performing employee. That is why we offer a stimulating environment, training opportunities, and long-term support in your career.

The position:

• Support quality validation activities within the framework of an ERP project in a pharmaceutical environment.
• Participate in the construction, review, and approval of validation protocols, test plans, and associated reports.
• Monitor the execution of test campaigns: SIT, UAT, E2E, FDR, while ensuring compliance with quality requirements.
• Verify requirements-tests traceability, documentary compliance, and the availability of validation evidence.
• Contribute to defect management: qualification, correction, re-test, documentation, and validation impact.
• Participate in the review of validation reports and quality closure decisions.
• Provide QA System support for the preparation of PPRs and the monitoring of associated actions.
• Lead the update of LSOPs impacted by the project, in connection with business SMEs.
• Administer quality documentation in Veeva Quality Docs: LSOP, GSOP, reports, plans, and records.
• Support users in the correct application of documentary and quality processes.

Profile sought:

• You hold a Master's degree (Bac+5) in Quality, Pharmacy, Engineering, Science, or equivalent.
• You have proven experience in a System Quality Assurance scope within the pharmaceutical industry.
• You master validation concepts: protocols, test plans, reports, requirements-tests traceability, and defect management.
• Experience on an ERP project, SAP, or other computerized system would be strongly appreciated.
• You are familiar with GSOP / LSOP documentary structures; mastery of Veeva Quality Docs is a real plus.
• You are comfortable with project and test tracking tools: ALM, Kneat, JIRA, SharePoint, or equivalents.
• You are rigorous, autonomous, methodical, and capable of working with cross-functional teams.
• You possess excellent communication and collaboration skills.
• Proficiency in English is necessary.