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Job Description

In this role, you will have the opportunity to ensure patient safety and regulatory compliance across the full product lifecycle for Hospital Patient Monitoring Portfolio by supporting medical product safety surveillance, adverse event reporting, and proactive risk management activities. You will contribute to timely and accurate safety reporting to regulatory authorities and internal stakeholders, analyze safety data from clinical and post‑market sources, and collaborate cross‑functionally to identify, assess, and mitigate potential safety risks. Your work will play a key role in safeguarding patient well‑being and maintaining compliance with global regulatory standards.

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