Role DescriptionIn this role you will be responsible you will be cooperating with several departments in order to achieve continuous improvenent
ResponsibilitiesCollaborating with the technical team, the IT teams and project managers Working closely with Operations Communicating with local and international customers, leading customers audits and providing support on quality control and quality assurance matters. Implementing a new Quality Management System (QMS), including improvement of quality reporting.
RequirementsMaster in a pharmaceutical-related subject. A minimum of a year of experience as a Qualified Person Experience with GMP en GDP. Demonstrable ability to communicate fluently (orally and in writing) and to present complex information Demonstrable experience with investigating, defining and resolving complex issues. Full professional prophecy in both Dutch and English. Demonstrable experience with planning, scheduling and monitoring work
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Greg Silberstein.