BrightOwl Loader Loading

Regulatory Affairs Assistant  Document Management Suresnes France,  

Product Life Group (company)


Posted on : 10 February 2017

Project Description



About Us:
  • Our company 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. 
  • Our company 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


 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  of work experience in a similar position  
  

Key skills 
  • Working as a team, collaborating and cooperating with others 
  • Develop positive contacts with the working environment 
  • Availability and willingness to learn 
  • Continuously seek to optimize knowledge and skills 
  • Propose alternative solutions to optimize the efficiency of the activity and the satisfaction of internal / external clients 
  • Adapt, be open to change 
  • Be rigorous 
  • Be meticulous 
  • Be organized  
  

Core competences 
  • Master of office tools (Pack Office etc &) 
  • Knowledge of Pharmaceutical Regulatory Affairs 
  • You are fluent in French and English for daily contacts with local and internationally partners.  
 

Benefits 
  • Competitive salary package 
  • Training and development 
  • International and growing company 
  • Dynamic environment  
 

Locations

Suresnes France

Find a Job Find Candidates

Similar Jobs

More jobs from Product Life Group

Other jobs in France

Other jobs in Suresnes

Other jobs from Product Life Group in Suresnes

Other similar job in Suresnes

Other Jobs

Most Recent Searches

Most Famous Searches

You might also like