Vetamc is seeking a Regulatory Affairs Liaison to coordinate regulatory activities across Europe and non-EU countries. The role involves managing submissions, developing regulatory strategies, and liaising with cross-functional teams, focusing on compliance and timely project execution
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.
Implement strategies for products in development with guidance and independently developing and executing strategies for registered products.
Liaise with HQ US-based cross-functional teams, effectively communicating regional requirements and ensuring compliance with all necessary regulations for assigned projects.
Matching Summary
Match Score: 85
Vetamc is seeking a Regulatory Affairs Liaison to coordinate regulatory activities across Europe and non-EU countries. The role involves managing submissions, developing regulatory strategies, and liaising with cross-functional teams, focusing on compliance and timely project execution.
Skills & Requirements
Must-have
EU regulatory requirements
product life cycle management
regulatory strategy development
regulatory documentation preparation
cross-functional team collaboration
Nice-to-have
strong organizational and planning skills
adapt to changing priorities
sound scientific knowledge
interpersonal communication skills
Key Requirements
Master's degree in pharmacy, chemistry, or equivalent
Minimum of 2 years of experience in the pharmaceutical industry