Pharmaceutical Regulatory Affairs – Publishing specialist
An innovating, dynamic and growing international pharmaceutical company is currently expanding their regulatory team in Switzerland, Vaud Canton.
Due to this growth they are 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
Please send your application to Jean de La Fournière: jean@axepta.com