Pharmaceutical Regulatory Operations Specialist

BE  ‐ Onsite
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Keywords

Description

A global pharmaceutical manufacturer is looking for a Regulatory Operations Specialist to support the technical writing of process documentation. This is a vital role supporting the Global Regulatory Operations department in Brussels.

Location: Brussels, Belgium
Duration: 6 months

Function and Responsibilities:

- Support process development and provide technical writing support
- Develop documentation (SOPs, User guides, technical guides) and training for a new content management system
- Deliver training to regulatory staff across Europe

Requirements:

- Pharmaceutical experience, preferably in R&D and Regulatory
- 2+ years` experience in delivering training to business users
- Preferably some experience with supporting content management systems
- Experience with Documentum, Firstdoc and Sharepoint
- Knowledge of Visio 2010 and Information Mapping

This is a fantastic opportunity to support the regulatory division of a leading pharmaceutical company.
Start date
ASAP
Duration
6 months
From
Quanta Consultancy Services
Published at
28.11.2012
Project ID:
454119
Contract type
Freelance
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