Lead detailed mechanical design and verification for an implantable medical device, ensuring manufacturability, regulatory-compliant V&V, tooling transfer to production, risk management (FMEA), and mentoring across cross-functional teams within a 24-month program.

Develop and implement safe, scalable, stable manufacturing processes across Cochlear and suppliers, ensure QMS and regulatory compliance, support supply chain and R&D projects, relocate/duplicate processes, apply lean principles, and drive continuous improvement to meet project timelines and cost targets.