Regulatory Affairs Administrative Assistant
Risch (Zug) Legal
Job description
Job Description
This position supports drug regulatory affairs matters in Switzerland, acts as a business partner within the country organization and interacts with Swissmedic in order to get new marketing authorizations, support timely product launches and secure regulatory compliance.
Within your role you are responsible for Products in different therapeutic areas.
You work in close collaboration with the Regulatory Managers to ensure together and under each one's role and responsibility, timely grant of Marketing Authorizations, timely product launches and regulatory compliance.
Desired profile
Your profile:
Pharmaceutical/technical/medical associate education or similar education
fluent in German and English, French / Italian desirable
Experience and know how in drug regulatory affairs and project management.
Knowledge on Swiss regulations and guidelines
Build know how on Quality Assurance and pharmaceutical technology.