Demonstrated experience in quality, supplier or customer audits, quality systems, compliance, clinical or laboratory operations, regulatory affairs, due diligence, or cross-functional program leadership within diagnostics, medical devices, biopharma, biotechnology, CROs, or a related regulated industry, typically gained through 8+ years of progressive experience. Proven ability to lead complex, multi-site or cross-business diligence activities and coordinate accurate responses across Quality, Legal, Regulatory, Privacy, Information Security, R&D, Clinical, Operations, Finance, and commercial stakeholders.