Principal Technical Program Manager

Job Description

This highly visible principal individual contributor role requires the ability to move between organizational strategy, engineering detail, and hands-on implementation. You will independently lead ambiguous, cross-functional programs, translate business and regulatory needs into technical requirements, and build tooling that reduces manual work and improves delivery.

You will work closely with Engineering, Product, Quality, Legal, and Regulatory Affairs to integrate medical device requirements into development and operational workflows. A key focus will be using automation to improve requirements tracking, documentation, evidence collection, and readiness for regulatory reviews, audits, certifications, and product releases.

As a strategic partner to the Director of Operations, you will also support organizational planning, resource allocation, and executive decision-making. Success requires technical depth, sound judgment, and the ability to influence senior stakeholders while delivering measurable improvements across teams.

Responsibilities

What You’ll Do:

• Lead Complex Technical Programs: Own cross-functional initiatives from problem definition through implementation. Establish technical requirements, milestones, dependencies, success measures, and accountability across Engineering, Product, Quality, Regulatory, and Operations.
• Build Automation and Internal Tooling: Design, prototype, implement, and maintain scripts, integrations, dashboards, and workflow applications using Oracle APEX, Python, SQL, APIs, or comparable technologies. Streamline intake, approvals, reporting, and program execution.
• Apply Codex and AI-Assisted Development: Use Codex and related tools to accelerate automation development, prototyping, testing, and documentation. Review and test generated outputs, applying appropriate controls when tooling supports regulated processes.
• Connect Automation With Medical Device Compliance: Partner with Quality and Regulatory Affairs to identify opportunities to automate requirements tracking, traceability, evidence collection, change tracking, and readiness reporting. Ensure solutions support applicable documentation, review, and validation requirements.
• Drive Medical Device Regulatory Readiness: Lead integrated plans supporting medical device certification, regulatory reviews, audits, and international expansion. Translate regulatory and quality requirements into actionable engineering and operational deliverables with clear ownership.
• Strengthen Technical Documentation: Coordinate Engineering and Product teams to produce complete, consistent, and traceable documentation supporting development, verification and validation, risk management, and product launches.
• Lead Release Readiness: Drive end-to-end release coordination, including engineering dependencies, quality and regulatory deliverables, readiness criteria, risk resolution, and stakeholder communication.
• Partner With Operations Leadership: Serve as a strategic thought partner to the Director of Operations. Support OP1/OP2 plan...

Lorem ipsum dolor sit amet, consectetur adipiscing elit. Sed do eiusmod tempor incididunt ut labore et dolore magna aliqua. Ut enim ad minim veniam, quis nostrud exercitation ullamco laboris nisi ut aliquip ex ea commodo consequat. Duis aute irure dolor in reprehenderit in voluptate velit esse cillum dolore eu fugiat nulla pariatur. Excepteur sint occaecat cupidatat non proident, sunt in culpa qui officia deserunt mollit anim id est laborum.

Sed ut perspiciatis unde omnis iste natus error sit voluptatem accusantium doloremque laudantium, totam rem aperiam, eaque ipsa quae ab illo inventore veritatis.