Siv Ghaffari

Siv worked in the Salt Lake valley for over two decades in biotechnology and pharmaceutical settings that include over 6 years of quality management and regulatory affairs experience. After 12 years working in the R&D division at Myriad Genetics and Myrexis (formally Myriad Pharmaceuticals), retooled by going back to school and getting Master of Science and Technology at University of Utah, and continued the career development by obtaining Regulatory Affairs Certification (RAC) for medical devices, Project Management Professional (PMP) Certification, and Certified Manager of Quality/Organizational Excellence (CMQ/OE). As the manager of Quality Assurance and Regulatory Affairs, it is the department’s primary goal to nurture a culture to maintain an effective and efficient Quality management System, that complies with global regulatory requirements and meets the challenges of developing, manufacturing and releasing of medical devices that are safe and effective for disruptive technologies, clinically cleared and research devices.