Regulatory Affairs Publishing and eCTD specialist

My client is an innovating, dynamic and growing international pharmaceutical company currently expanding their regulatory team in Switzerland, Vaud Canton.

Due to this growth my client is looking for a Regulatory Affairs Publishing and eCTD specialist to join them on a permanent contract.

Responsibilities:

Supporting Publishing and EDMS (Electronic Document Management System) users
Business Administrator for Publishing and EDMS systems
Archiving Submission Dossiers
Provide training and support for Publishing and EDMS users
Manage related training materials
Perform Business Administration activities for Publishing and EDMS
Archive Submission Dossiers and ensure their traceability across systems
Interface with Coordinators from Consumer and Aesthetic SIGs and with IT team
Support writing of procedures, instructions, user guides
Ad interim, could act as delegate of the Publishing coordinator for outsourced activities

Your profile:

BSc, MSc in scientific, IT or administrative discipline or equivalent experience
Minimum 3 years’ experience Pharmaceutical Industry
Minimum 2 years’ in similar role