Elissa P Jones

Elissa P. Jones serves as a Contract Specialist responsible for managing the full lifecycle of procurement actions for specialized medical equipment, ensuring compliance with federal acquisition regulations and agency mission objectives. She plays a pivotal role in executing competitive acquisitions, evaluating technical proposals, negotiating contract terms, and administering performance obligations for electromedical and electrotherapeutic devices. Her work directly supports the delivery of critical healthcare technologies by aligning procurement strategy with clinical and operational requirements, often coordinating with technical evaluators, legal counsel, and program managers to ensure acquisition integrity and mission readiness. While no specific contractor relationships are currently identifiable in the dataset, Jones engages with a broad spectrum of manufacturers and suppliers specializing in advanced medical device technologies. Her procurement approach emphasizes competitive bidding, full and open competition, and rigorous source selection under FAR Part 15 procedures. She maintains professional relationships with industry partners who demonstrate technical expertise, quality assurance certifications, and reliable delivery capabilities in the electromedical space. Jones demonstrates a clear preference for full and open competition, with 100% of her acquisitions classified as “No Set-Aside.” This reflects a strategic focus on maximizing market competition and selecting the most technically capable offerors, regardless of socioeconomic status, while still ensuring compliance with all small business programs where applicable. Her approach prioritizes performance outcomes over socioeconomic preferences, aligning with mission-critical procurement needs. Her primary procurement focus is exclusively under NAICS 334510, which encompasses the manufacturing of electromedical and electrotherapeutic apparatuses such as TENS units, neuromuscular stimulators, and diagnostic therapeutic devices. She possesses deep domain expertise in the technical specifications, regulatory standards (including FDA clearance pathways), and clinical applications of these devices, ensuring acquisitions meet stringent safety, efficacy, and interoperability requirements.