Sr Manager Global Trade Compliance - Trade Programs

It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do  a global leader in robotic-assisted surgery and minimally invasive care, our technologies-like the da Vinci surgical system and Ion-have transformed how care is delivered for millions of patients worldwide.

We're a team of engineers, clinicians, and innovators united by one purpose: to make surgery smarter, safer, and more human. Every day, our work helps care teams perform with greater precision and patients recover faster, improving outcomes around the world.

The problems we solve demand creativity, rigor, and collaboration. The work is challenging, but deeply meaningful-because every improvement we make has the potential to change a life.

If you're ready to contribute to something bigger than yourself and help transform the future of healthcare, you'll find your purpose here.

The Senior Manager Global Trade Compliance Trade Programs is responsible for the development of the strategies, policies, processes, tools and solutions that anchors our trade compliance programs, including but not limited to, global import and export classification, country of origin, trade preferential, supply chain security (C-TPAT, AEO), export control / license determination, and other trade compliance programs. The ideal candidate would be a subject matter expertise of global trade regulations and experience with customs operations with a strong track record of delivering projects that involves coordination across different functions (e.g. tax, supply chain, etc.).

• Develop, implement, and maintain the relevant trade compliance policies, procedures, manuals, and standard work documents necessary to successfully manage import and export operations and trade programs.
• Manage compliance and oversee trade programs including classification, ECCN, preferential and non-preferential origin, Customs valuation, duty suspension, duty drawback, supply chain security, ADD/CVD, etc.
• Supervise daily trade program activities, processes, and documentation requirements, setting the standard and conducting audits for accuracy and regulatory adherence.
• Monitor inquiries from Customs authorities and coordinate response timely (e.g.; CF28, CF28, Customs audits, etc.
• Responsible for the Customs reconciliation and anti-boycott programs.
• Audit and maintain data governance in SAP and global product database and applicable trade compliance records in accordance with regulatory requirements.
• Provide accurate trade data element including product classification, ECCN, country of origin, license determination to internal business units and outside service providers to ensure compliance with Customs regulations and other trade requirements.
• Work with global trade compliance operations and external partners such as customs broker, freight forwarders, to execute strategies, drive and enforce global import/ export processes, seek automation opportunities and leverage technologies.
• Provide global customs and trade compliance guidance to programs that will result in cost-saving and duty avoidance opportunities.
• Identify tariff engineering opportunities where applicable.
• Build flexible and scalable solutions across various customized technologies, business models/ supply chain arcs, and country regulatory regimes.
• Manage, mentor, and develop staff including hiring, goal setting, performance, coaching, teamwork, and projects.
• Serve as a subject matter expert on customs compliance matters, providing guidance and support to internal stakeholders on complex issues and transactions.
• Participate as core team member on new product development, new market launch, new product launch ensuring that all trade compliance requirements are met.
• Communicate risks, proposals, regulatory updates and strategies to internal and external stakeholders.
• Assist Regional Trade Compliance managers in researching Customs- and regulatory requirements for new destination markets including classification, import licenses, valuation, documentation, and import- and export restrictions and communicate back to medical device business.
• Submit and monitor import/ export permit/ license applications as needed.
• Interact with IT and