In this role, you will be responsible for local regulatory activities, including the preparation of SmPC–PIL (KÜB–KT) and coordination with internal departments.
Requirements
Graduated from Pharmacy, Chemical Engineering, Chemistry, Biology, or similar
Preferably 1 year of experience in registration
Familiar with pharmaceutical terminology
Good command of English
Responsibilities
Managing the preparation and approval of SmPC–PIL documentation
Following up on regulatory-authorization processes
Preparing responses to health authorities
Coordinating communication with relevant departments
