Engineering Program Manager

Responsibilities may include the following and other duties may be assigned

• Lead planning and execution of large, cross-functional engineering programs supporting Neuromodulation and Pelvic Health therapy platforms.
• Translate therapy strategy and business priorities into integrated, executable program plans across software, systems, firmware, and hardware.
• Drive program governance, risk management, and decision-making aligned to FDA and global regulatory standards, including IEC 62304, ISO 14971, and Design Controls.
• Ensure early and sustained integration of Quality and Regulatory partners throughout the development lifecycle.
• Own complex dependency management across teams, suppliers, and global sites.
• Lead design readiness, milestone reviews, and design transfer to operations, ensuring compliance, documentation completeness, and manufacturing readiness.
• Proactively identify risks, trade-offs, and mitigation strategies; escalate with clarity and recommendations.
• Provide executive-level communication on program status, risks, and strategic implications.
• Lead and influence senior cross-functional stakeholders across R&D, Quality, Regulatory, Clinical, Operations, and Supply Chain.
• Own integrated schedules, resource strategies, and delivery commitments aligned to therapy and portfolio objectives.
• Act as a trusted execution partner to OU and MEIC leadership.
• Support portfolio prioritization through data-driven insights and lessons learned.
• Mentor program managers and technical leads, raising execution maturity across teams.
• Provide functional leadership to program teams and vendors operating with high autonomy.
• Coach and mentor peers and junior program managers to elevate delivery excellence.
• Travel up to 25%, as required.
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Required Knowledge and Experience