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Regulatory Affairs Assistant  Document Management Suresnes France,  

Posted on : 10 February 2017

Project Description

LOCATION: Suresnes France Fixed term contract ProductLife Group is the European industry-leading specialist service provider for the Life Sciences industry, focused on delivering high quality professional services in the areas of Regulatory, Safety, Quality, Process alignment and Medical services. All ProductLife Group s services are targeting support for comprehensive compliance and safety throughout the product life cycle, therefore enabling continuity and productivity of product development and subsequent processes.   As a result of the deployment of a new project we are now seeking a Regulatory affairs assistant document management   Primary Responsibilities Contribute to the production of administrative documents in pharmaceutical regulatory Check the format of translations and modify if necessary Formatting tables and text fields Inserting data Creation of duplicated translations Compile files and regulatory documents in accordance with prerequisites Transformation of document formats Formatting media Management of the review of texts Review format of the documents Systems Management and Administration Entering metadata Importing and indexing documents Bibliographic searches   Candidate profile Education: Bachelor degree in a science related field Experience: 3 to 5 years minimum


Suresnes France

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