Lead a complex global development program for a regulated medical equipment platform combining console hardware, electronics, software, system integration, and launch execution. The role aligns a globally distributed cross-functional team and external partners to deliver phased releases, regulatory and operational readiness, and market expansion. The position leads a strategic medical device platform program spanning hardware, electronics, software, systems integration, regulatory readiness, manufacturing readiness, service readiness, and launch execution. It owns the integrated end-to-end program plan across phased releases, connecting development, verification and validation, documentation, supply chain readiness, field readiness, and commercial launch activities. The leader drives alignment across engineering, quality, regulatory, operations, service, marketing, finance, and leadership stakeholders, clarifying priorities, dependencies, risks, decisions, and ownership. The role partners with internal operations teams and external manufacturing partners to prepare product configurations for release, scale-up, and ongoing platform evolution. It also leads formal design, business, and readiness reviews, with disciplined follow-through and timely escalation of issues that threaten cost, quality, scope, or timing. The role brings execution rigor and improves coordination, transparency, and decision-making without unnecessary process burden. This is an office-based role in Bedford, Massachusetts. Office-based teams work in person at least three days per week. Candidates must reside in or within commuting distance of Bedford, MA. US work authorization is required; sponsorship is not available, and relocation benefits will not be provided.
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Job Type
Full-time
Career Level
Senior