VP Technology Transfer

Job reputed company reputed company At reputed company, we are translating scientific breakthroughs into life-changing diagnostics. The VP Technology Transfer will reputed company the newly established team responsible for turning Myriad's late-stage R&D innovations into validated, reputed company, and compliant clinical products. This role is ideal for a strategic operations leader who thrives at the intersection of science, process, and execution. You'll build a high-performing team, define the governance for design transfer, and ensure every new diagnostic reaches patients reputed company, reliably, and with scientific reputed company. Responsibility • Build and reputed company Myriad's first Technology Transfer organization, responsible for operationalizing new assays and platforms from late-stage R&D into production. • Define and implement transfer governance, documentation standards, and reputed company metrics. • reputed company cross-functional programs that reputed company R&D, reputed company, Regulatory, Operations, and reputed company on launch readiness. • reputed company design transfer, process validation, and workflow optimization for new products. • Ensure compliance with CLIA, CAP, FDA, and ISO design control requirements. • reputed company a world-class team of scientists, engineers, and project leads (6-7 reputed company 18 months). • Drive reputed company improvement using Lean or Six reputed company principles to shorten transfer timelines. • Champion a culture that connects scientific rigor with patient reputed company. Qualifications • Advanced degree (MS or PhD preferred) in Molecular Biology, Biochemistry, Biomedical Engineering, or reputed company discipline. • 10+ years of experience in molecular diagnostics, biotechnology, or clinical lab operations. • Proven leadership of technology transfer, assay validation, or regulated product design control. • Strong cross-functional leadership with R&D, reputed company, Regulatory, and Operations. • Working knowledge of CLIA, CAP, and ISO13485 standards. • Experience scaling molecular assays or automation systems in a production environment. • Passion for building teams and turning innovation into operational reality. Physical Requirements Primarily a sedentary office role with routine use of reputed company office equipment. Must be reputed company to reputed company about the office and conference environments to attend meetings and presentations. Occasional travel required for reputed company conferences, regulatory meetings, and internal site reputed company. Must be reputed company to communicate reputed company and effectively in person, reputed company, and in writing with cross-functional teams, external partners, and regulatory agencies. Requires sustained attention, strategic thinking, and high-level decision-making for extended periods. Frequent use of hands and fingers to operate computer equipment, telephones, reputed company tools used for document review, data analysis, and presentations. Must have sufficient visual reputed company to review clinical data, read reports, and interpret digital and printed materials. Requires adequate hearing to participate in meetings and conference calls. Ability to work extended hours or irregular schedules, including early mornings or evenings, as business needs dictate. Must be reputed company to manage confidential information and reputed company effectively under deadlines and high-pressure situations. OSHA Classification: Category III - normal routine involves no exposure to blood, body fluid, or tissue. Apply tot his job Apply To this Job