Your tasks
PAION Pharma is a specialized pharmaceutical company headquartered in Aachen, Germany and part of the Humanwell Healthcare Group. Our focus lies on products in anesthesiology, intensive care and infectious diseases, primarily for use in hospital environments, supporting healthcare professionals in clinical practice.
For our growing team in Aachen we are looking for an experienced Associate Director Regulatory Affairs.
In your role you will ensure the marketability of our products and contribute to our commercial success.
You will be responsibble for the
For our growing team in Aachen we are looking for an experienced Associate Director Regulatory Affairs.
In your role you will ensure the marketability of our products and contribute to our commercial success.
You will be responsibble for the
- Management of Marketing Authorizations in various countries (EU, UK, US, JP, etc.)
- RA management of license partners
- CTD submission management (e.g. variations, extensions, renewal, etc.)
- Strong support for Clinical Development
- Responsible for regulatory interactions with authorities (e.g. pre-submission meetings, scientific advice meetings, authority questions etc.) including documentation management
- Establishing and implementing regulatory strategies with respect to company goals
- Leadership for the maintenance of IB, PBRER, DSUR, CCDS and other documents
- SOP management