Job DescriptionRegulatory Affairs Consultant – Zurich
An exciting opportunity has arisen in a world renowned pharmaceutical client to be based in the Zurich area. They have a well-established portfolio and an excellent pipeline of products. Your role will be to deliver the life cycle plans for the pipeline products and ensure regulatory compliance of registered products at EU and country level.
- CMC regulatory post-approval support of commercial small molecule products in the EU over the lifecycle of each products
- Key liaison between the company with EU and individual country bodies. Build a strong working relationship with internal and external stakeholders as a representative of the company.
- Contribute to the performance led culture in the cross-functional environment.
- Active collaboration with areas of Quality, PV, Medical Affairs, Market Access and Marketing
To apply for the role, please submit your application with an updated CV in any format. If you have questions about the role, or you would be interested to discuss other regulatory affairs contract roles, get in touch with me, Kevin Kendaru.
Experience in within the EU is essential. Please note we can only accept applications from candidates who hold valid European Union passport and are able to work in Europe without visa sponsorship. Fluent English is required, German is an advantage.
It’s people that deliver projects and with over 60 offices in 33 countries, at NES Global Talent we have access to the best talent wherever it may be in the world. If you are interested to see what other roles are available in Regulatory Affairs in Switzerland, please send an updated CV in any format to email@example.com.