Dominique Liégeois

Global Business Owner for the SAP Document Management System (DMS) module.
Developed e-learning programs and acted as Business Project Leader for the revision project of the document management process and its supporting tool.

Pilots for migration of SAP Controlled Documents in Veeva Quality Documents.

Development of bots to automatise activities to facilitate the migration.

Managed Regulatory Inspections and Pharmacovigilance activities.

• Ensured regulatory compliance through meticulous auditing procedures.
• Successfully managed risk assessment procedures by adopting industry best practices.

Project Manager for the SAP Maintenance, Calibration & Measurements module. Led roll-out projects (version 3) at Godollo, Hamilton, and Marietta sites.
GBO Support: end-user assistance, management of change requests for system improvements.
Project Manager for the SAP Master Data module.
Led Global Operations Toll roll-outs in Singapore, Ste-Foy, Hamilton, Godollo, Dresden. Contributed to the Incoming Raw Materials project.
GBO Support: end-user assistance, change request management for system enhancements.

Global Business Owner for the SAP Document Management System (DMS) module.
Deployed SAP modules and established an implementation methodology covering all project organization aspects.
Developed e-learning programs and served as Business Project Leader for the revision of the document management process and its supporting tool.

• Organised networking events to build industry connections and partnerships.

Conducted GMP internal quality audits and equipment requalification expertise. Experience in batch record corrections and internal audits.
SAP Phase 3 + Audimat Key User: requirements writing, testing and validation, drafting manuals, training, and end-user support.
Developed multiple QA applications to streamline daily work.
KPI Representative; developed tools for simplification and automation of calculations.
Served as liaison between Customer Service, Planning, and local QA priorities.
IT expert for QA secondary manufacturing; SAP trainer for both local and global QA (QM module and Audimat).

• Regularly reviewed operating procedures, enhancing productivity and reducing waste.
• Ensured adherence to health and safety regulations at all times, promoting a safe work environment for everyone.
• Participated in regulatory audits, ensuring company's adherence to industry standards.
• Identified potential risks by performing regular audits on production lines.

Worked in Manufacturing at GSK Rixensart.
Protein purification using column chromatography and ultracentrifugation, column packing, GMP compliance,
sterile filtration and vaccine formulation, aseptic environment work,
drafting validation and production protocols, writing procedures, planning, filter integrity testing certification at Millipore, environmental monitoring.

• Prioritised tasks efficiently, met tight production deadlines on a consistent basis.
• Facilitated speedy resolution of quality control issues by appropriately escalating concerns to Production Manager.
• Maintained high production standards by following precise operating procedures.