Marc A. Flores

Marc A. Flores serves as a Contract Specialist responsible for managing the full lifecycle of federal acquisitions, from requirements definition through contract award and administration. He plays a critical role in ensuring compliance with the Federal Acquisition Regulation (FAR) while supporting mission-critical procurement needs within the health technology and medical equipment sectors. His portfolio primarily involves competitive sealed bidding and negotiated procurements for specialized medical devices, surgical supplies, and electromedical systems, requiring deep technical understanding and precise contract language to meet stringent regulatory and performance standards. While specific contractor names are not available, Flores consistently engages with a diverse base of vendors, including small businesses and manufacturers with expertise in medical device production and healthcare instrumentation. His working relationships reflect a preference for responsive, technically capable suppliers capable of meeting exacting quality and compliance standards, often through multiple-award contracts and indefinite-delivery/indefinite-quantity (IDIQ) mechanisms that support agile, long-term sourcing needs. Flores demonstrates a strong commitment to small business participation, with over 27% of his acquisitions structured as set-asides under FAR Part 19. His primary focus is on Total Small Business Set-Asides, complemented by targeted use of Service-Disabled Veteran-Owned Small Business (SDVOSB) set-asides. This pattern reflects a deliberate effort to expand economic opportunity while maintaining a robust supplier base capable of delivering specialized medical equipment and services. His procurement focus centers on NAICS codes related to surgical and medical instrument manufacturing (339112), surgical appliance and supplies manufacturing (339113), and electromedical apparatus production (334510), indicating deep expertise in the medical device supply chain. He also routinely procures related services under NAICS 811219, suggesting involvement in repair, maintenance, and calibration of clinical equipment. His technical domain expertise spans regulatory compliance, risk mitigation in medical procurement, and the unique lifecycle requirements of Class I and II medical devices under FDA oversight.