Director, Government Affairs

We are seeking a candidate local to the North American HQ office in Mahwah, NJ

A secondary location of Washington D.C. would be acceptable, with monthly visits to the NJ HQ office.

Join Mindray North America and help shape the future of patient care.

Mindray is a global leader in medical technology, delivering advanced patient monitoring systems, anesthesia machines, ventilators, and ultrasound solutions trusted in hospitals and critical care environments worldwide. Unlike many larger competitors, Mindray combines cutting‑edge innovation with unmatched value, giving healthcare providers access to reliable, feature‑rich technology without compromise. Our culture is built on collaboration, integrity, and a drive to equip caregivers with the tools they need to deliver exceptional care.

Fast facts about Mindray:

• Founded in 1991, with 14,000 employees worldwide
• 8 global R&D centers, investing ~10% of annual revenue into innovation
• North American headquarters in Mahwah, NJ, with 40+ international subsidiaries

The Director of Government Affairs will develop and implement comprehensive government relations strategies aligned with corporate priorities. This leader will monitor healthcare policy developments, assess legislative and regulatory risks, and proactively shape policy outcomes that impact medical device approval, reimbursement, trade, and healthcare innovation.

This role requires deep knowledge of the healthcare and regulatory landscape, exceptional communication skills, and the ability to navigate complex policy environments with agility and influence.

• Develop and execute federal and state government affairs strategies aligned with corporate growth objectives.
• Monitor, analyze, and interpret legislative and regulatory developments affecting medical device approval pathways, reimbursement structures, trade policy, and healthcare innovation.
• Provide strategic counsel to the President and executive leadership regarding policy risks, emerging opportunities, and regulatory shifts.
• Shape and advance advocacy priorities that support long‑term business objectives.

• Establish and maintain strong, productive relationships with key government agencies, healthcare regulatory bodies, centralized procurement entities, medical insurance organizations, and international institutions including Centers for Medicare & Medicaid Services (CMS), Adva Med, WHO, UNDP, and UNICEF.
• Cultivate and maintain relationships with Congressional offices, executive branch agencies, and key policymakers.
• Actively participate in industry coalitions and contribute to the development of policy positions that advance the medical device sector.
• Represent the organization at industry events, policy forums, conferences, and meetings with government officials and external stakeholders.

• Partner cross‑functionally with sales, marketing, regulatory affairs, and legal teams to ensure advocacy efforts align with product strategy, commercialization goals, and regulatory positioning.
• Translate complex policy developments into actionable insights for internal stakeholders.

• Track and evaluate healthcare funding mechanisms, allocations, and reimbursement models within the designated market.
• Provide regular, actionable reporting on policy changes, including regulatory updates, market access developments, and import/export controls.
• Influence legislative and regulatory outcomes affecting medical device approval pathways and market access.

• Identify, assess, and mitigate risks arising from trade disputes, policy shifts, or regulatory changes that could impact operations.
• Develop and implement proactive risk mitigation strategies.
• Ensure full compliance with lobbying disclosure requirements and ethics regulations.
• Oversee external lobbying firms and consultants where applicable.

• Bachelor's degree or higher in a relevant field such as public health, pharmacy, medical science, public policy, economics, international relations, communications, or marketing.
• Minimum of 8 years of…