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Regulatory Affairs and Quality Specialist - Global Pharma

Business Type: Pharmaceutical Company, Pharmaceutical Services
Job Type: Regulatory Affairs
Job Level: Experienced (non manager)
Position: Full Time
Location: Italy
Reference: PC.68104.1
Closing Date: 20/05/21
Job Details:

NonStop Pharma is looking for a Regulatory Affairs and Quality Assurance Specialist, to join a global pharmaceutical group, leader in cardiovascular and metabolic diseases, oncology and immuno-inflammatory, and neurodegenerative diseases.


  • With direction, develop and execute regulatory project plans
  • Identify and elevate key areas of regulatory risk
  • Participate as an active team member and provide regulatory advice to project teams as required
  • Respond to questions from regulatory authorities within strict time lines
  • Participate as an active team member and provide role-based regulatory advice to project teams as required

Who I am looking for:

  • Knowledge of regulations on centralised procedures EMA submissions and Product registrations
  • Scientific knowledge
  • Project management skills
  • Manage multiple projects and deadlines
  • Ability to multitask and prioritize

If you want to be part of the global development of safe and effective medical therapeutics through its scientific and disciplined approach, submit NOW your CV to Patrick Carignano -

NonStop is one of the largest and fastest growing specialised life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. We have a strong presence within Italy as well as Germany, Switzerland, France, The Nordics and Benelux. Please visit our website for a full list of the

Posted: 13/05/2021 | NPJ Ref: 270619
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