Role DescriptionYou will work within a quality team together with two other colleagues and you will report to the head of quality.
Responsibilities-transfer support of new products to Operations -contact suppliers & subcontractors: documentation, batch record reviewing, deviations & process validation -final product release -stability studies -customer complaint handling -CAPA reports
Requirements-GMP and/or ISO 13485 knowledge; -2 years experience in a similar role; -2years experience in a pharmaceutical company; -master’s degree (Pharma, Biotech, Life Sciences); -speaking and writing fluently Dutch and English; -organizational and analytical skills; -mature & assertive; -teamplayer and excellent communication skills;
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Rutger Koning.