Provides technical assistance for all phases of contracts within Offices/Divisions. Uses own judgment to independently write or rewrite performance work statements for solicitations, re-solicitations, and follow-on contracts. Independently designs and performs contract quality assurance for each requirement. Exercises management oversight of obligation of expenditure of funds and establishes internal controls to prevent fraud, waste, and abuse. Finalizes changes to contracts for content, format, and acceptability. Advises management and staff on all contract current and proposed policies. Recommends changes to existing policies and procedures. Determines whether contractor performed work meets standards of adequacy before authorizing payment. Finalizes contracts and solicitations to ensure appropriate quality control requirements are imposed prior to submission to FDA, Office of Acquisitions and Grants Services (OAGS).

Coordinates regulatory science research projects and activities.Participates in acquisition planning, statement of work (SOW) development, team meetings, and assures stakeholder engagement as appropriate.Contracting Officer's Representative (COR) FAC-COR Level III. Manages all actions for major contracts to include development of procurement requirements, pre-award and post award requirements to oversight and contract close-out.

Manages assigned contracts within the Office of Pharmaceutical Quality as the lead Contracting Officer’s Representative (COR).Executes a variety of actions supporting FDA’s national commitment to science education as liaison for the office’s Oak Ridge Institute for Science and Education (ORISE) Fellowship Training Program.

Coordination activities oversee administration, facilities, procurement, and operations while directly assisting the Director and Deputy Director in the financial management of key research programs.Directs the actions of the division's Safety Team, Equipment Maintenance Team, and the Facilities Infrastructure Team.

Evaluate scientific data in the area of hematology in vitro diagnostic medical devices and submits reports on a variety of regulatory actions. Interactively reviews, provides direction and guidance to medical device manufacturers regarding the scientific data used to evaluate in vitro diagnostic device 510(k) submissions.

Supervise the Hematology Department located within the clinical laboratory.Assure that blood specimens submitted for testing in the Hematology Department meet laboratory guidelines.Train personnel in the use of laboratory equipment.Oversee whole blood glucose monitoring system for hospital staff of 383 employees, generating 18,178 results annually.Detect and resolve discrepancies in patient results.Maintain special chemistry instruments located in the clinical laboratory.Produce accurate and timely results according to laboratory policy.Collect quantities of blood by venipuncture and capillary methods as appropriate for patient age and/or condition.Perform and record quality control function checks with the specified time frame.

Perform and document preventative maintenance on laboratory instrumentation.Detect and resolve discrepancies in patient results.Produce accurate and timely results according to laboratory policy.Insured that all Material Safety Data Sheets (MSDS) were current in laboratory and notified staff of any harmful chemicals contained in testing reagents.Organized continuous quality improvement effort for Colorado River Service Unit and was team leader for this committee.