Junior Regulatory Affairs Manager (m/f)

REFERENZNUMMER:

368454/11

IHRE AUFGABEN:

-Marketing authorization applications for drugs and medicinal products (e.g. new marketing authorisations, line extensions, etc.)
-Obtain and assess the marketing authorization documentation and compile and customize it to meet the local requirements of Swissmedic in collaboration with HRA and/or RAM
-Be a competent and reliable contact for representatives of Swissmedic
-Tracking Databases
-Make sure that local laws and guidelines as well as Pfizer SOPs are always met
-Guarantee the submission in time

IHRE QUALIFIKATIONEN:

-Academic degree in natural sciences (pharmacy, chemistry, biochemistry, biology or medicine)
-Knowledge of or experience in project management techniques is of advantage
-Clear verbal and written communication
-Very good knowledge of German (native speaker) and English, good knowledge of French, knowledge of Italian is an advantage
-Good computer skills
-Knowledge of the current Swiss regulatory and drug laws environment is of advantage
-Knowledge of pharmaceutical analytics technology, pharmacology, toxicology and medicine

WEITERE QUALIFIKATIONEN:

Regulatory affairs manager, Project manager