QA Medical Devices Specialist

Develop and maintain a quality management system which complies with ISO 13485, MDR, MDD and other applicable medical device standards and regulations.

Contribute to the maintenance of the Otsuka Europe quality system in order to ensure that quality assurance and regulatory compliance activities are fully adequate, and that Otsuka Europe fully complies with all relevant medical device legislation and industry recommended practice.

Quality Assurance - Develop and maintain the quality management …