We are seeking an experienced and motivated professional to join our software quality assurance team. In this key role, you will help ensure compliance with IVDR, FDA 21 CFR Part 820, and cybersecurity requirements for medical device software. - Solid knowledge of quality management systems and standards (IEC 62304, IVDR, FDA 21 CFR 820, ISO 14971) With thousands of employees across six continents, collaboration is our greatest strength. Join us, grow with us, and together, let's shape the future of biological discovery. - Partner with development teams to support compliance with internal procedures and external regulations - Review and approve software development documentation in in
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