Supports corporate and securities matters for a Nasdaq-listed medical device company, including SEC and Section 16 filings, insider trading administration, board and stockholder meetings, contracts, legal operations, equity programs, entity management, corporate records, and healthcare compliance. The role also administers legal technology systems, coordinates with transfer agents and outside counsel, and supports employees and executives with equity and legal requirements.

Leads process development and design transfer for catheter devices from early-stage configurations to commercial manufacturing. Responsibilities include DFM/DFA, tolerance analysis, catheter and electrical assembly process optimization, validation, FMEAs, SPC, measurement studies, supplier qualification, sterilization compatibility, lean improvements, ECOs, documentation, and cross-functional collaboration. Mentors junior staff and supports production readiness in a regulated medical-device environment.