Tonia Washington

Tonia Washington serves as an Acquisition Specialist responsible for managing the full lifecycle of procurement activities related to surgical and medical instrument manufacturing. In this role, she ensures compliance with federal acquisition regulations while aligning purchasing decisions with operational needs and mission objectives. She typically handles complex, high-precision solicitations for Class II and Class III medical devices, including surgical tools, diagnostic instrumentation, and sterile-reusable equipment, often requiring adherence to FDA regulatory frameworks and ISO 13485 quality standards. Her work supports critical healthcare delivery systems through strategic sourcing and risk-mitigated contract execution. While specific contractor relationships are not currently documented, Tonia engages with a broad spectrum of manufacturers and suppliers qualified under federal procurement standards, including both large-scale OEMs and specialized niche vendors with expertise in medical-grade materials and sterile packaging. Her contracting approach emphasizes technical evaluation, performance-based requirements, and supplier qualification through rigorous pre-solicitation market research and vendor capability assessments. Tonia’s procurement patterns reflect a strong preference for open competition, with 100% of her acquisitions classified as “No Set-Aside.” This indicates a focus on technical merit and product performance over socioeconomic preferences, though she remains fully compliant with all small business outreach and reporting obligations under FAR Part 19. Her approach prioritizes capability and compliance, ensuring the highest standards of safety and efficacy in medical instrumentation. Her primary NAICS focus—339112 (Surgical and Medical Instrument Manufacturing)—demonstrates deep specialization in the design, production, and procurement of precision medical devices. She routinely evaluates technical specifications for sterility, biocompatibility, and regulatory certification, making her a subject matter expert in the intersection of manufacturing standards and clinical requirements within the federal healthcare supply chain.