Quality Associate

Your role:

To provide quality support to reMYND’s activities at the DDD and CRO unit:

• Reviewing in-vivo and in-vitro studies from start to finish: documentation and data analyses

• Preparing and realizing study- and process-based quality inspections, follow-up with operators and study directors

• Managing lab and facility-related equipment: keeping databases and log books up to date; coordinating (internal and external) validation, calibration, maintenance and corrective efforts

• Managing non-conformities: active participation in and evaluation of root cause investigations; impact assessments (MEA) and corrective and preventive actions (CAPA)

• Supporting the optimization of quality-related business processes e.g. implementation of new equipment & database systems • Supporting further realization of safety and animal welfare standards including maintaining an SDS and chemical inventory

• Working in a team of equal-minded colleagues under the supervision of the Quality Manager

• Planning your own activities on a weekly basis in order to deliver committed results

Your background, skills and attitude:

• Holder of a bachelor's or master’s degree in biology, bio-medical science or biotechnology

• General knowledge of quality guidelines (GLP) with initial experience in a quality position is a plus

• A result-oriented, outgoing attitude with a high level of energy; able to work closely in a team; eager to learn

• Familiar with MS Word and an advanced MS Excel user

• Fluent in Dutch and English