Responsibilities- Ensuring that Manufacturing quality systems are established, maintained and documented according to needs of the business, customers and applicable quality system standards & regulations; - Updating and creating training material for the Quality system; - Provide oversight of Q&R manufacturing projects ensuring timely completion of project deliverables, correcting issues delaying completion and reporting on quality system status of projects on manufacturing department or site level; - Developing and administering schedules, performance requirements; - Acting as advisor to subordinates to meet schedules and/or solve technical problems; - Following processes and operational policies in selecting methods and techniques for obtaining solutions.
Requirements- Bachelor or Master degree in Industrial Engineering, or other technical field; - Project and process management experience; - Affinity with Quality and Regulatory within medical devices or other such regulated industry; - Demonstrated ability to understand and develop processes. - Demonstrated ability to interact and communicate in Dutch and English, including demonstrable writing, speaking, and comprehension skills; ability to communicate across levels of the organization. - Analytical and great attention to detail;
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Robin Hiariej.