Pharmaceutical Regulatory Affairs – Publishing specialist

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