Possesses versatile skills in project management, problem-solving, and collaboration. Brings fresh perspective and strong commitment to quality and success. Recognized for adaptability and proactive approach in delivering effective solutions.
Overview
6
6
years of professional experience
Work History
Manufacturing Validations Specialist
BAMF Health
Grand Rapids, MI
01.2026 - Current
Developed and implemented process improvements to enhance operational efficiency.
Analyzed data trends to inform decision-making and optimize workflows.
Evaluated existing processes, identifying areas for enhancement and cost reduction.
Managed project timelines, ensuring deliverables were met on schedule and within scope.
Supervisor, Nuclear Manufacturing
Cardinal Health
12.2024 - 01.2026
Directed daily aseptic manufacturing operations (ISO 5/7), including vial filling, sterility testing, and bulk material production, ensuring compliance with FDA 21 CFR Part 212.
Led cross-functional collaboration with CMOs (GE Healthcare) to align production schedules, quality agreements, and validation activities.
Oversaw equipment qualification and validation (GC, HPLC, TLC, Cyclotron, HEPA), ensuring readiness for regulatory inspections.
Hired, trained, and requalified technicians in aseptic techniques, achieving a 90% increase in site efficiency and top performance metrics for FY25.
Reduced investigations by 48% through proactive CAPA implementation and process improvements.
Senior QA Specialist
Cardinal Health
06.2023 - 12.2024
Reviewed and approved all production batches (FDG, NaF, O-18 Recycling, Vizamyl, Ga-68, Zirconium-89), equipment validations and change controls.
Coordinated with pharmacy and production teams to ensure on-time delivery of radiopharmaceuticals.
Implemented tracking systems for media fills, visual inspections, and equipment maintenance, improving compliance and efficiency.
Developed and standardized QC procedures, reducing overdue maintenance and investigations.
Nuclear Lab Technician II
Cardinal Health
02.2022 - 06.2023
Produced and tested sterile radiopharmaceuticals (FDG, NaF, bulk F-18) under ISO 5 and ISO 7 conditions.
Performed QC assays (TLC, GC, pH, BET endotoxin, HPLC) and sterility testing on all products.
Qualified in media fills and obtained authorized user (cyclotrons) license.
Managed inventory and ensured uninterrupted production readiness.
Property Management Service Rep.
Ablelight/Bethesda
04.2020 - 04.2022
Managed multiple shared inboxes (maintenance, AP, leasing, real estate development).
Implemented Yardi Voyager software and generated 80+ weekly operational reports.
HR Recruiter
Ablelight/Bethesda
11.2019 - 04.2020
Managed recruitment and hiring processes, strengthening organizational and communication skills.