**In this role, you will have the opportunity to** ensure patient safety and regulatory compliance across the full product lifecycle 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.
**Your Job**
+ Support the timely and accurate evaluation, documentation, and reporting of adverse events from multiple sources, including post‑market surveillance, literature reviews, and real‑world data, in accordance with applicable regulatory requirements.
+ Analyze safety data from clinical trials and post‑market surveillance to identify pot...