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Senior Regulatory Affairs Project Manager

  • Job type: Permanent
  • Location: Liège Angleur
  • Salary: £100000 per annum
  • Job reference: Jordan Veglio
  • Sector: EPM Scientific, Regulatory
  • Date posted: 20/04/2018

I am working on a regulatory affairs project manager for a huge CMO located in Belgium. The company opened the door to the biggest gene therapy manufacturer in history.  
You would actually be the only person in medical device at the site. It is a hugely exciting position, for a massive company that would open a lot of doors.



In this position, you will be:
  • Provides RA support to site and customers. Prepares, submits and maintains  necessary dossiers and import/export licenses for the site
  • Fulfills Regulatory  activities in support of the site and customer  goals including submission scheduling across the network
  • Evaluation of current processes and systems with regard to industry best practices, available resources, and evolving regulations and guidelines and propose changes targeting greater efficiency and continued compliance.
  • Co-ordinates and supports Lonza regulatory information for the Verviers site
  • Anticipation, evaluation and implementation of trends and innovations in the RA arena.
  • Contributes to the development, implementation of procedures and processes.
  • Provides technical expertise and consulting to technical and business strategies.
  • Develops and maintains high level contacts with external RA stakeholders including customers, regulatory authorities, academic institutions, scientific experts as necessary
  • Develops and maintains relationships among the Lonza worldwide RA function.
 
 
 
 
 
 
 
 
 


If interested, please send me your CV to apply.a33ho1gnv23@epmscientific.aptrack.co.uk
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