Responsible for leading the BWI and BioPark sites for Catalent, where we offer development, clinical and commercial gene therapy CDMO services.

General Manager leading Thermo Fisher Scientific's Advanced Therapies Business, which includes our CDMO services for plasmid DNA, mRNA, and Cell Therapies. This role is responsible for many talented colleagues across multiple sites in the US and Europe. Together we enable our customers to bring life changing therapies and vaccines to patients around the globe leveraging our capable teams and leading-edge technologies.

Responsible for Thermo Fisher Scientific's Microbial Manufacturing and mRNA Manufacturing CDMO businesses with locations in the US and Europe.

Responsible for Operations at our Carlsbad, CA site and contract site in Watertown, MA offering high-quality, robust, GMP plasmid / microbial manufacturing CDMO services enabling our clients to make the world healthier.

General Manager of the Cambridge, MA Site. Part of the Viral Vector Services unit within the Pharma Services Group at Thermo Fisher Scientific.

General Manager of the Alachua Site. Part of the Viral Vector Services unit within the Pharma Services Group.

Responsible for the site operations at the Alachua campus.

Responsible for leading our German Operations towards improved profitability for our global organization while effectively collaborating with the functional leaders at corporate and other sites across our international footprint.

Coordinating and leading the organization's initiative to solidify and standardize processes across the growing and diverse global enterprise within one unified ERP platform. Responsible for developing and implementing the roadmap for system and process integration that will support the organization's strategic growth plans, while strictly adhering to budgetary and timeline requirements.

Leading the management team of our 250+ employees in Operations towards developing, executing, and continuously improving systems and processes for achieving manufacturing excellence as defined by our safe working environment, our product cost and quality, our customer service levels, and the morale and engagement of our teams.

Responsible for coordinating best practices of production activities and key performance indicators among our global Operations departments.

Led a cross-functional team-based approach to optimize corporate logistics from material procurement through processing and distribution.

Managing centralized and celluar analysis efforts performed by Operations Analysts and Material Control Planners within the different Business Units in Operations with a focus on cost and delivery.

Responsible for performing high-level capacity, constraint, resource allocation, and cost absorption analyses for the Operations group.

Developed and managed an MRP system for the Global Supply Chain business unit allowing for the cost-effective procurement and release of supplies and other consumables for manufacturing.

In addition to the responsibilities associated with the position as the Director of Global Ops, I have also been asked to directly manage the Production Planning, Standard Costing & Production Analysis, Order Processing, Product Packaging & Label Development and Finished Goods Warehouse & Shipping departments at the German facility. This position affords me the opportunity to apply and improve my experiences in fields such as Supply Chain Management, Medical Devices, Cost Accounting, and People Leadership in a non-US/non-English Speaking culture.