Bachelor's degree in Computer Science, Engineering, or related field., Proven experience in software quality assurance and testing, preferably in the medical devices industry., Strong knowledge of regulatory standards such as ISO 13485 and FDA guidelines., Excellent analytical and problem-solving skills..
Key responsibilities:
Oversee the quality assurance process for software development in medical devices.
Develop and implement testing strategies to ensure compliance with industry standards.
Collaborate with cross-functional teams to identify and resolve quality issues.
Prepare and present quality reports to stakeholders and management.
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Materialise empowers sustainable 3D printing applications. We provide pioneering solutions that enable flexible industrial manufacturing and mass personalization in healthcare. We rely on more than 30 years of experience in additive technologies to provide various software and services to support your projects, make a difference, and realize your potential. We lead the way by delivering end-to-end solutions in multiple industries — innovating with companies for a better, healthier, and more sustainable world. For additional information, please visit: http://www.materialise.com/.