The Quality Expert Medical Device Software will support the review and maintenance of assigned processes of the Quality Management System and will as well support the development and commercialization of assigned Medical Device Software Projects are conducted in accordance with Quality System requirements, ensuring high product quality, regulatory compliance and operational efficiency. The responsibility includes ensuring that new medical device software products including web-based and mobile applications are developed, commercialized and maintained through ist lifetime in compliance with medical device, software and data security regulations and standards.
Quality Assurance - Medical Device
Global pharma company
Are you looking to work in a global growth company where you can make a real difference? Then you are right with us!
Relevant Educational Degree
As per Industry
Practical experience in managing projects in compliance with ISO 13485, 21 CFR part 820 / part 4, IEC 62304, IEC 82304, ISO 14971, IEC 62366, MDD/MDR, GDPR and other relevant standards and guidances related to medical device software with atleast 3 years of experience. Good knowledge of medical device software development and life-cycle management is required
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If you are interested then kindly send your resume to email@example.com