Role DescriptionThis is still a young and developing company, and your experience will determine what kind of responsibilities you can pick up in the organisation. You will be part of a young and dynamic team, which will give you the space and opportunity to grow, learn and give your own input. Together you will shape the course of this company and get to be part of the organisation (both strategically and financially). Above all this job means freedom, flexibility and independence.
Responsibilities- Batch record review and - if you are a certified QP - batch release; - Validation tasks relating to the clean room and the lab; - Optimalisation of the SOPs; - Deviations, CAPAs and change controls.
Requirements- MSc. Life Sciences; - GMP & GDP knowledge or experience; - Experience in Quality - An entrepeneurial mindset; - A hands-on mentality and wanting to contribute to the company on a strategic level.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Cees Roffelsen.