Eu, uk, switzerland, non-eu see regulatory coordination
Implement product development strategies
Manage submissions and interactions with eu agencies
39med is seeking a Regulatory Affairs Liaison to coordinate regulatory activities across the EU, UK, and Switzerland, focusing on product development and compliance. The role requires strong communication skills and regulatory knowledge to manage submissions and liaise with cross-functional teams
Job Summary
Coordinate regulatory activities in the EU, UK, Switzerland, and non-EU SEE countries under the supervision of the (Senior) Principal Scientist of Regulatory Affairs.
You will be responsible for implementing strategies for products in development with guidance and independently developing and executing strategies for registered products.
Additionally, you will play a crucial role in managing submissions and interactions with the EU regulatory agencies.
Matching Summary
Match Score: 85
39med is seeking a Regulatory Affairs Liaison to coordinate regulatory activities across the EU, UK, and Switzerland, focusing on product development and compliance. The role requires strong communication skills and regulatory knowledge to manage submissions and liaise with cross-functional teams.
Skills & Requirements
Must-have
EU, UK, Switzerland, non-EU SEE regulatory coordination
Implement product development strategies
Manage submissions and interactions with EU agencies
Liaise with US cross-functional teams
Coordinate regulatory documentation preparation
Nice-to-have
Build and maintain scientific knowledge
Adapt to changing priorities
Work in international environment
Key Requirements
Master's degree in pharmacy, chemistry, or equivalent
Minimum of 2 years of experience in pharmaceutical industry