Join Baxter’s Regulatory Affairs team and make a direct impact on how innovative medical devices reach patients safely across Greater Asia. In this role, you’ll design and implement regulatory strategies, secure product approvals, and ensure compliance with evolving requirements. You’ll be hands‑on in shaping Baxter’s portfolio, working across new product development, post‑market activities, and regional projects—all while building your expertise and influence in a dynamic healthcare environment.

• Apply your medical device experience to drive regulatory success.
• Develop and execute project plans that keep approvals on track.
• Identify and escalate regulatory risks early, ensuring proactive solutions.
• Stay ahead of international regulatory requirements and translate them into clear, actionable steps.
• Be an active contributor on project teams, offering practical regulatory advice.
• Respond to re...