Meet our Quality Assurance Team

After completing my Master of Pharmacy degree in 2008, I began my career in pharmaceutical manufacturing, where I quickly developed a strong interest in Quality Assurance. Today, I am registered as a Qualified Person (QP) in the European Union in accordance with Article 48 of Directive 2001/83/EC.

I have extensive experience in quality systems, regulatory compliance, and quality leadership, with a proven track record of implementing effective QA frameworks and driving continuous improvement initiatives. My expertise includes problem-solving, auditing, risk management, and regulatory compliance across GMP and GDP environments.

As a QA consultant, I enjoy working collaboratively with clients and stakeholders to strengthen quality systems, optimize processes, and deliver practical, risk-based solutions that support business and compliance objectives.

After earning my Master’s degree in Medical Biology from Radboud University in Nijmegen, I gained more than 7 years of experience in GMP-regulated environments in the cell and gene therapy industry. My background includes both manufacturing operations and leading Quality Management System (QMS) activities as a QA Officer and Team Lead. Since joining Interdos as a Senior QA Officer in March 2024, I have further expanded my expertise in Good Distribution Practice (GDP) and currently serve as Responsible Person (RP) for multiple clients. I am a structured and detail-oriented professional who remains calm under pressure and values open collaboration. I enjoy supporting clients and partners in achieving excellence in quality and compliance.

After completing my vocational Bachelor’s degree as a Medical Laboratory Technologist in Belgium, I started working in the pharmaceutical industry in 2012 as a live viral vaccines production technician in a GMP-regulated environment. I later gained experience in quality management systems and people management as a cell therapy manufacturing team leader within a contract development and manufacturing organisation (CDMO), before further developing my Quality Assurance experience as a QA Associate. 

I joined Interdos as a Senior QA Officer in August 2024 and currently serve as Responsible Person (RP) for several clients. I am a thorough and open professional with a continuous improvement mindset. I enjoy supporting clients and contributing to partnerships while maintaining a strong focus on quality and compliance.

I am a quality professional with a background in Molecular Biotechnology and broad experience in pharmaceutical GMP environments. Over the years, I have worked across Quality Control and Quality Assurance, combining hands-on laboratory knowledge with experience in quality systems, investigations, compliance and continuous improvement. 

In my role as Senior QA Officer at Interdos, I support clients with practical QA solutions, always keeping both GMP requirements and day-to-day operations in mind. I enjoy working closely with people, understanding their specific challenges and finding clear, workable solutions. Having worked in international and fast-changing environments, I am comfortable adapting quickly while maintaining a strong focus on quality and compliance.

After completing my Bachelor’s and Master’s degrees in Biomedical Sciences at Maastricht University, I gained several years of experience in the biotech industry before transitioning to Regulatory Affairs in the medical device industry. This provided me with a strong foundation in regulatory compliance, Quality Management Systems (QMS), change control, and auditing.

Since joining Interdos as a QA Officer in April 2025, I have further developed my expertise in Quality Assurance, Good Manufacturing Practice (GMP), and Good Distribution Practice (GDP). I currently work as a Senior QA Officer and serve as Responsible Person (RP), supporting clients with quality and compliance activities in pharmaceutical distribution.

I am a calm, reliable, and detail-oriented professional with a structured approach to my work. I enjoy collaborating with colleagues, clients, and partners and supporting organisations in maintaining and continuously improving their quality systems.