Assess quality events and propose improvements towards Supervisor
Write and review documentation (SOP’s, Quality Instructions, protocols) related to quality control activities.
Contact person for specific projects/ tasks/ non-routine activities/ deviations. Can support complex issue's and has technical writing skills
Contribute to Quality Councils, EM excursion reports or investigation
Involved in planning activities in cooperation with the Supervisor Quality Control.
Working with contractors
Contribute cross-departmental initiatives.
Qualifications
The position requires a very precise and responsible working attitude.
Intermediate or higher vocational education in chemistry/biotechnology.
Extensive experience with GMP and good knowledge of incoming materials, EM, microbiological (gram stain, sterility) or analytical (RT-qPCR, FACS, ELISA) techniques depending on the area of interest.
Good communication skills in English.
Accuracy, tidiness, self-organized, flexible, attention to detail.
Team player
Education & qualification: Bachelor or Master within the relevant discipline 5-10 years of relevant experience. Flexibility, work must be finished. Dutch working permit
