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Use innovative regulatory approaches and provide strategic regulatory guidance for assigned projects/products. Develop and implement regulatory strategies, integrating inputs from regulatory team and cross functional partners to build globally aligned
You will act as a trusted quality and compliance advisor. You will help teams navigate complex regulatory requirements, strengthen quality processes, manage risk and continuously improve the way clinical trials are delivered. Monitor the regulatory
In this role, you will help ensure that our medical device products and quality processes meet applicable regulatory requirements and international standards. Working closely with colleagues across product development and the wider organization, you will
You will lead the development and execution of global regulatory strategies in close collaboration with co-development partners and internal and external stakeholders. Acting as regulatory lead for complex projects, you will draw upon
Ensuring the timely generation of a wide range of clinical regulatory documents required for the development of novel therapeutic agents from discovery up until and beyond marketing approval. This includes providing hands-on scientific/medical writing