Curriculum Vitae

Curriculum Vitae Bert Van Peteghem (last update on 18 JUL 2025):

• June 2025 – Current: Quality Consultant (20%) @ Delta-Pharma, Pharmaceutical Wholesaler, Bilzen, Belgium
  Responsible Person (RP) for compliance with Good Distribution Practices (GDP), including update of Delta-Pharma’s Quality Management System (QMS)
• June 2024 – August 2025: Quality Consultant (60-80%) @ Andocor, Manufacturer Medical Devices (catheters open heart surgery), Hoogstraten, Belgium
  Validation (Clean Room, Sterilization), Project Manager (PM) Medical Device Regulations (MDR) Implementation, Interim QA-RA Lead
• May 2023 – May 2024: Athena (Organon’s SAP) Lead Internal Quality (Executive Director of Quality), Organon, Global
  Quality Lead for SAP implementation (Q Module – Batch Disposition Cockpit) at 6 internal manufacturing sites
• December 2016 – April 2023: Site Quality Head (Executive Director of Quality), MSD/Organon, Heist-op-den-Berg, Belgium
  Lead of the entire Quality Unit: Quality Control, Quality Assurance, Quality Systems and Compliance (~250 FTE). Principal Qualified Person (QP) of the Heist site including Steriles, Liquid/Ointments/Creams, Tablets and Packaging
• April 2016 – December 2016: Site Quality Head Ad Interim (Executive Director of Quality), MSD, Heist-op-den-Berg, Belgium 

• March 2011 – December 2016: Lab Lead (Director of Quality), MSD, Heist-op-den-Berg, Belgium
  Lead of the Quality Control Lab (~130 FTE) including Analytical, Microbiological, Incoming Inspection Labs, Stability Department, Calibration & Support, Validation & Tech Transfers
  • May 2015 – July 2015: Lab Stabilization Project, Merck Wilson facility, North Carolina, USA

• January 2007 – February 2011: Plant Qualified Person, Specialties Plant / High Value and Manual Operations (HV&MO), MSD/Schering-Plough Labo, Heist-op-den-Berg, Belgium
  Lead the Specialties Quality Unit (~10-15 FTE), including Batch Release, Batch Record Review, Deviation/Out of Spec Handling, Complaint Handling, Change Control and Annual Product Reviews
• February 2003 – December 2006: Disposition & Quality Improvement Manager (DQI) Sterile Products, Schering-Plough Labo, Heist-op-den-Berg, Belgium
  Implement and Lead the Quality Unit for Sterile Products (~10-15 FTE), including Batch Release, Batch Record Review, Deviation/Out of Spec Handling, Complaint Handling, Change Control and Annual Product Reviews
• September 2001 – February 2003: QC Specialist Sterile Products, Schering-Plough Labo, Heist-op-den-Berg, Belgium
  Certification as Qualified Person (QP) and Batch Release of Sterile Products