We are looking for a QA Officer for our QA department in Leiden, The Netherlands. The QA team is responsible for the quality support in our vaccine development programs and performs all relevant activities related to product development and production of clinical trial material. As a QA Officer you will be responsible for:
- Maintain and support the quality management system
- Document, Change, Quality Incident and CAPA Control
- Review manufacturing and assay batch records
- Execute internal audits; follow up on audit observations during internal and customer audits
- Support the supplier qualification program
- Together with your QA colleagues you will ensure proper quality in customer projects.
You will join a stimulating group of international researchers in a very collaborative environment. This QA officer position reports to the Director QA / QP.
Your letter of motivation and CV should show that you have:
- A Bachelor / Master degree in life science, biotechnology or related subject;
- At least two years’ experience in a biotechnology or biopharmaceutical industry environment as QA Officer;
- Experience with viral vectors and/or viral vaccines is a plus;
- Experience with performing audits of facilities, systems or suppliers is a plus.
- Good command of the English language (written and spoken).
In the interviews it will be clear that:
You are enthusiastic and comfortable in a dynamic environment. You can work both in a team and individually. You communicate clearly at all levels; you can get your thoughts, ideas and knowledge across in a helpful way. You enjoy to train manufacturing personnel in quality aspects. Your planning and organization skills allow you to have an overview of the necessary work and you are able to meet deadlines.
You can send your motivation letter and resume to Mrs. Ingrid van Aarle, HR Manager firstname.lastname@example.org
Application by agency or recruiters is not appreciated and will be rejected.
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