Technologiepark-Zwijnaarde 94, Ghent, Belgium
Performing QA related and supportive activities for the GMP compliant production and quality control of Investigational Medicinal Products (IMPs).
Performing QA document review of the manufactured products and quality supportive activities/services like calibration, monitoring of clean rooms, cleaning of equipment.
Incoming quality control of raw materials and critical goods.
Support the qualification of production and test equipment.
Support the supplier qualification process.
Support the QA manager/Qualified Person in the maintenance of the Quality Management System and the CAPA system.
You will report to the QA Manager/Qualified Person.
A minimum of a Bachelor Degree preferably in life science with two (2) years of experience in a GMP pharmaceutical production environment or equivalent by experience.
You have basic knowledge of Quality Management in a regulated environment (Eudralex GMP, ICH, FDA).
You are flexible, quality minded and well-organized.
You are fluent in English (written and spoken).
Work in a fast growing organization.
A position with responsibility within a dynamic company.
Personal development through learning on the job and additional external trainings.
A market oriented compensation.
Please send us your motivation letter and CV through our career site: https://jobs.smartrecruiters.com/Eurofins/743999745633043-qa-officer