Are you a person who always driving by an urge to get the best results and do you have experience within the GMP of the pharmaceutical industry? Then keep on reading!
Role DescriptionFor our quality department we are looking for a Qualified Person for a period of 5 - 7 months. As a Qualified Person your most important task will be to monitor the implementation of the quality regulations. Besides you will also be responsible for the execution and review of the quality regulations. You will work with different quality systems which have to meet the current GMP standards. In addition the job includes the implementation of internal audits, deviations, validation of the processes and complaint management.
The function is very diverse and your days will never be boring. All these tasks you will perform in a team of professionals with affinity for the pharmaceutical industry.
ResponsibilitiesYou are responsible for: - The implementation of the quality regulations - Monitoring and reviewing the execution of the quality regulations - Operating the quality systems - Streamlining the validation of the processes - Internal audits, complaint management and deviations
RequirementsWe are looking for someone who: - Has a PharmaD or BSc in pharmacy - Has at least 2 years experience as Qualified Person - Has good knowledge of current Quality regulations - Speaks both English and Dutch fluently - Is a team player and eager to learn - Having experience as an QP is a plus
Other informationWe offer you an inspiring and educational working environment and the possibility to make a difference.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Ria Bos.