This is a great opportunity for you to work as a Quality Director for an innovative brand within the medical industry.
As the Quality Director you will be responsible for compliance, quality and regulations across the business. You will lead the quality management and regulatory affairs team in the continuous development and implementation of ISO13485 and 21 CFR 820.
As well as having experience with the above you will also need to have the following;
Must have previous experience working as a Quality Director or Senior Quality Manager
Experience with standards such as ISO 13485, 21 CFR Part 820 and ISO 14971
Experience auditing to ISO 13485
Experience managing a team of people
Must speak fluent German and English
If you wish to apply please contact Emily wright
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