Pioneer regulatory strategies for medical devices, ensuring timely global approvals, compliance, and quality. Collaborate across teams, mentor peers, and tackle complex submissions for US, EU, and beyond in a hybrid work environment.

Optimize production efficiency by leading manufacturing operations across multiple areas; drive continuous improvement initiatives alongside engineering to achieve quality, cost reduction, and safety compliance, while fostering team engagement and accountability.

Drive the global controlled document lifecycle, establishing standards and governance to enhance quality. Lead cross-functional collaboration for consistent execution, ensuring compliance and continuous improvement across the organization.

Drive regulatory strategies for medical device approvals globally, ensuring compliance. Collaborate across teams to prepare submissions and lead initiatives that enhance operational efficiency while mentoring junior staff for successful delivery.

Strategize process improvements by deploying lean methodologies, coordinating cross-functional initiatives, and analyzing performance metrics to enhance operational efficiency, reduce waste, and achieve annual targets through collaborative efforts.