Brenda M. Ferjak

Brenda M. Ferjak serves as a Contract Specialist responsible for managing the full lifecycle of federal acquisitions, from market research and solicitation development to contract award and administration. Her work supports critical procurement missions involving specialized medical and diagnostic equipment, ensuring compliance with federal acquisition regulations and promoting efficient, transparent contracting practices. She routinely handles complex procurements under FAR Part 12 and Part 15, focusing on commercial items and competitive negotiated contracts for high-precision medical technologies. While specific contractor names are not available, Ferjak maintains consistent working relationships with a broad base of suppliers in the medical device and diagnostic manufacturing sectors. Her procurement patterns reflect a preference for established commercial vendors with proven quality systems and regulatory certifications, including FDA-registered manufacturers. She engages both large-capacity producers and small businesses, fostering competitive environments that prioritize technical capability, supply chain reliability, and regulatory compliance. Ferjak’s contracting portfolio is predominantly non-set-aside, with 88.6% of awards issued under full and open competition. However, she actively supports small business participation, with over 10% of awards directed toward Total Small Business Set-Asides under FAR 19.5 and a notable 1.1% allocated to Service-Disabled Veteran-Owned Small Businesses. Her approach reflects a balanced commitment to socioeconomic goals without compromising acquisition efficiency or mission readiness. Her technical expertise centers on NAICS codes 325413 (In-Vitro Diagnostic Substance Manufacturing), 339112 (Surgical and Medical Instrument Manufacturing), and 339113 (Surgical Appliance and Supplies Manufacturing), reflecting deep specialization in diagnostic reagents, precision surgical tools, and medical disposables. She also engages with 811219 (Other Medical and Dental Equipment and Supplies Repair) for maintenance and calibration services. Ferjak’s domain knowledge spans regulatory frameworks including FDA Class I–III device classifications and ISO 13485 quality standards, enabling her to effectively evaluate technical proposals and ensure compliance with health and safety mandates.