Role DescriptionIn this role you will become the QP for the company and act as QP for GMP related activities. You will also help in other QA related activities (CAPA, deviations, ...) and ensuring compliance within the company.
Responsibilities- Establishment of Quality Agreements - Act as Qualified Person Deputy for GMP related activities - Ensure the release of Investigational Medicinal Products in compliance with applicable regulation - Ensure contact with Belgian Competent Authorities - Assist in internal and external Audits - Review Batch records, CAPA, Change Controls, deviations, ...
Requirements- Qualified Person (Belgian registration) - Fluent in French and English - Excellent communication and intercultural skills - Team worker and team spirit - Customer oriented
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Laura Hoekstra.