Donna W Raday

Donna W. Raday serves as a Contracting Officer responsible for managing complex procurements within the federal acquisition system, with a primary focus on medical and surgical equipment manufacturing and distribution. She executes full and open competitions and set-aside acquisitions in accordance with FAR Part 19, ensuring compliance with statutory requirements while delivering mission-critical supplies to support healthcare operations. Her portfolio encompasses the full lifecycle of contract actions—from market research and solicitation development to award and administration—emphasizing technical precision, regulatory adherence, and efficient resource allocation to meet agency needs. While specific contractor names are not available, Raday’s contracting patterns indicate consistent engagement with manufacturers and wholesale distributors specializing in precision medical devices, analytical laboratory instruments, and surgical supplies. Her procurement approach favors established industry suppliers with demonstrated technical capability and quality assurance systems, fostering long-term vendor partnerships grounded in performance reliability and regulatory compliance. She maintains a balanced procurement strategy that supports both large-capacity manufacturers and qualified small businesses. Raday exhibits a strong preference for full and open competition, with 85.6% of her awards issued without set-asides. However, she actively promotes small business participation, allocating 12.8% of awards to total small business set-asides under FAR 19.5 and an additional 1.6% to 8(a) competed contracts. This reflects a deliberate effort to integrate socioeconomic goals into routine acquisitions without compromising mission readiness or technical requirements. Her industry focus centers on NAICS codes 339112 (Surgical and Medical Instrument Manufacturing), 332322 (Sheet Metal Work Manufacturing), and 334516 (Analytical Laboratory Instrument Manufacturing), indicating deep expertise in procuring high-precision, regulated medical hardware and supporting components. She routinely acquires specialized equipment requiring stringent quality controls, including sterilization compliance, ISO certifications, and FDA-regulated manufacturing processes, demonstrating technical fluency in the medical device supply chain.