Guide the operations of the Non-Profit through Board advisory and hands-on volunteering. Manage the email communications and web site (interim). Act as "Swamper" to clear the trails of fallen trees and storm damage. Adopted several trails to trim back the vegetation growth to keep the trails open and accessible to the public.

As a member of Veeva's Medical Device & Diagnostics service team, optimize client quality, regulatory & clinical data and documentation processes. Actively listen to client global needs, translate requirements into solution design, and define global strategies for deploying Veeva could-based solutions for managing quality, regulatory & clinical information across the enterprise.

Led programs and projects for the Life Sciences industry, providing business continuity during M&A activity, compliance in response to regulatory authority demands, and achieving efficiencies at every opportunity.

Develop and execute regulatory risk strategies for pharmaceutical and medical device companies. • Assessed quality management system for medical device manufacturer, prioritizing remediation recommendations.• Led the development of a quality analytics dashboard, enabling leadership to manage in near-real time the health of the organization.• Established a contract conversion process for divested biopharma and med device company, resulting in 60 IT Commercial contracts signed before separation day 1.

Specialist Master, Life SciencesProvide supply chain standards adoption support within the commercial and federal healthcare space. Subject matter expertise on regulations such as UDI, DSCSA, pedigree & serialization, and GS1 / HIBCC data standards.• Led teams to develop strategy and implement global UDI and GS1 solution at medical device manufacturer accounting for all three classes of devices and several hundred thousand products.• Developed business case for Veterans Affairs’ data standards office, GS1 as core standards, enabling effective operations and patient safety through centralized and standardized data practices.Specialist Master, Supply ChainPlan and execute contract separation as a result of spinoffs and divestitures.• Gathered and catalogued 800K contracts using automation and manual QC for one of the world’s largest investment banks in response to the SR14 regulation of Dodd-Frank act.• Executed IT RFP process and contract separation project to position $6B flour milling business for start-up.

Business development driving supply chain standards adoption within the U.S. foodservice and healthcare industries. • Developed business process impact map for product ID (GTIN) and data synch (GDSN) implementation.• Drafted comments in response to regulations such as FDA UDI proposed rule and Electronic Health Record (EHR) Meaningful Use, serving as both author and subject matter expert on regulations.• Instituted SLAs, integrated project plans, knowledge base support practices, and dashboards in program management of commercial software, resulting in stable infrastructure and repeatable processes.

Managed IS portfolio for and partnership with Global Clinical Supplies operation through alignment of business, regulatory & IT strategies. Oversaw up to 25 internal and contracted staff with annual budget of $7.5MM. • Reduced projected annual spend by $10MM by leading delivery of supply chain management ERP system with forecasting capability, operational automation, and master data inventory, earning two Merck Awards.

Director Data Operations, QA & Regulatory Systems Manager Directed staff, processes, data quality, and P&L for IT operations, including data center and company-wide infrastructure. • Established strategic goals and positioned company for 21CFR11 and ISO9001 compliance to ensure competitive advantage in marketing GCP applications to pharma/biotech industry.