Mathieu Van Schel

QC Manager | Business Unit Manager at Eurofins BioPharma Product Testing

Greater Paris Metropolitan Region

About

With more than 10+ years of experience in the pharmaceutical industry across France, Belgium and Germany, I have built my career from analytical R&D and Quality Control to Business Unit leadership. Today, I lead GMP laboratory operations by combining scientific expertise, operational excellence and business management to deliver high-quality services in regulated environments. As Business Unit Manager at Eurofins BioPharma Product Testing, I lead multiple Quality Control laboratories to deliver reliable, high-quality analytical services that meet our customers' needs and supporting them throughout the lifecycle of their pharmaceutical products.

Experience

  • Eurofins Biopharma Product Testing (France) (6 yrs 9 mos)
    • Business Unit Manager - QC Small molecules
      Sep 2022 - Present · 3 yrs 11 mos

      Leading the QC Small Molecules Business Unit within Eurofins BioPharma Product Testing, with full accountability for business performance, laboratory operations, quality compliance and strategic development. Business Leadership - Full P&L ownership - Management of CAPEX, budget and operational KPIs - Leadership of various GMP QC laboratories (i.e. HPLC, GC, ICP-OES/AAS, Physico-Chemistry and Packaging Testing) - Management of external laboratory partnerships Business Development & Operations - Development of new analytical services in collaboration with commercial teams - Laboratory expansion and infrastructure development - Continuous improvement through Lean Management and operational excellence - Digital transformation through ELN, eLIMS and Quality Management System deployment Quality & Compliance - Ensure GMP compliance across the Business Unit - Involved in customer audits and regulatory inspections - Drive quality culture and continuous process improvement Global Responsibilities - French Representative – Eurofins BioPharma Global Compendial Council (Raw Materials Testing) - French Representative – Eurofins BioPharma AI Council

    • Deputy Laboratory Head - QC Small molecules
      Jan 2022 - Sep 2022 · 9 mos

      Supported the Business Unit Manager in leading the BioPharma QC small molecules Business Unit, while preparing full transition Leadership - Deputy Manager of five GMP QC laboratories (60+ FTE including Laboratory Managers, Project Managers, Data Reviewers and Analysts) - Direct management of the External Partners organization - Monitoring business and laboratory performance through operational and financial KPIs - Contributing to the strategic growth of the Business Unit Operational Excellence - Coordinated daily laboratory operations across multiple analytical platforms - Led Lean Management initiatives, 5S deployment and laboratory optimization projects - Supported the implementation of new analytical services Quality - Ensured compliance with GMP, internal procedures and quality standards - Laboratory representative during customer audits and ANSM regulatory inspection (2022) Global Role - French Representative – Eurofins Global Compendial Testing Council

    • Laboratory Manager - Group Leader Wet Chemistry
      Nov 2019 - Dec 2021 · 2 yrs 2 mos

      Managed the Physico-Chemistry laboratory within the BioPharma Product Testing division, focusing on operational excellence, people development and laboratory performance. Team Leadership - Managed a multidisciplinary team of 20+ FTE - Recruitment, coaching and development of laboratory personnel - Performance management through operational and financial KPIs Laboratory Management - Responsible for the Physico-Chemistry and PSD laboratories - Coordinated laboratory activities with Metrology, Quality Assurance and IT departments - Led Lean Management, 5S deployment and laboratory organization improvements Scientific & Technical Leadership - Oversaw routine GMP testing activities - Designed analytical studies including method development, validation and transfers - Supported business development through implementation of new testing capabilities Quality - Responsible for OOS, OOT and laboratory investigations - Ownership of CAPA plans and continuous improvement actions - Active participant during customer audits and regulatory inspections _____________________________________ Group Leader (Jan2020-Dec2021) Team Manager (Nov2019-Jan2020)

  • R&D Engineer at Baxter International Inc.
    Mar 2016 - Nov 2019 · 3 yrs 9 mos

    Progressively expanded responsibilities within the Analytical Center of Excellence and Clinical Nutrition Global Business Unit, combining scientific expertise with laboratory supervision and operational improvement: Research & Technical Expertise - Designed and led analytical studies for particle characterization - Supported EMEA manufacturing sites during OOS, OOT and troubleshooting investigations - Provided technical expertise to Customer Complaint Investigation teams Laboratory Leadership - Supervised the Microscopy and Cytotoxic Drugs laboratories - Monitored laboratory performance through KPIs - Led Lean Management and 6S deployment - Member of the Site Laboratory Cohesion Committee Quality - Ensured compliance with Baxter Quality Management System - Developed studies in accordance with GMP and internal quality standards Additional Responsibilities - EHS Committee member and qualified trainer - Mentoring of interns ____ R&D Clinical Nutrition GBU (Oct. 2018 - Nov. 2019) R&D Analytical Center of Excellence (Mar. 2016 - Oct. 2018)

  • Trainee, R&D Engineer at Solvay
    Feb 2015 - Jul 2015 · 6 mos

    Conducted research projects within the Soda Ash & Derivatives Research & Innovation Center, supporting process optimization and analytical method development: - Designed experimental studies from literature review to industrial-scale implementation - Developed Process Analytical Technology (PAT) solutions for in-line monitoring - Developed analytical methods for monitoring chemical equilibria and phase transitions - Collaborated with multidisciplinary R&D teams to improve industrial processes

  • Trainee, Engineer R&D at Merck KGaA, Darmstadt, Germany
    Jul 2013 - Jun 2014 · 1 yr

    Worked within the Analytical Chemistry R&D Troubleshooting Laboratory, supporting pharmaceutical investigations related to particulate matter in drug products : - Investigated particulate contamination in pharmaceutical products - Performed advanced material characterization using Optical Microscopy, Polarized Light Microscopy (PLM), Raman Spectroscopy, FTIR and SEM/EDS - Conducted investigations in compliance with GMP and GDP requirements - Contributed to root cause analyses supporting product quality and manufacturing

  • Internship, R&D Analytical chemistry at CPE Lyon
    May 2013 - Jun 2013 · 2 mos

    Method development/validation for plasticizer and super-plasticizer additives using UV-spectroscopy