• Manage the implementation and maintenance of the Zutphen QMS, ensuring compliance with ISO standards.• Facilitate internal and external audits for warehouse certifications, leading to successful outcomes.• Oversee incoming inspection activities, ensuring quality standards are met.• Troubleshoot sterilization issues and provide project support, improving efficiency and quality control.

Developing a test-specific, single-use microfluidic cartridge at a diagnostic startup company. Overseeing the entire project cycle, from initial planning and design to final closure, collaborating with cross-functional teams and external partners. Implementing best practices to enhance efficiency, reduce costs, and increase productivity. Additionally, ensuring product quality and regulatory compliance, leveraging analytical skills, problem-solving abilities, and attention to detail. Driven by innovation and excellence, dedicated to delivering high-quality, diagnostic solutions for clients and patients.

Working for a service provider to biotech companies in the global IVD medical device market, providing clients with IVD tests that make state-of-the-art medical diagnostics possible. My responsibilities include overseeing the verification and validation studies from the initial planning and design stages to the final closure of the project.

Responsible for the planning and execution of the required lab activities including supervising and guiding interns and technicians, data analysis, troubleshooting and resolving issues that arise during the projects.

Perform and analyze development and validation experiments using a wide spectrum of immunoassay techniques and immunoassay devices.