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Job Details
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Regulatory Affairs CMC - Veneto

Business Type: Pharmaceutical Company, Pharmaceutical Services
Job Type: CMC, Regulatory Affairs
Job Level: Experienced (non manager)
Position: Full Time
Location: Italy
Reference: PC.68130.1
Closing Date: 21/05/21
Job Details:

NonStop Pharma is currently looking for an experienced Regulatory Affairs Specialist, experienced withing the CMC part, to join one of the most interesting APIs plants in North Italy.

They have an interesting and established product''s portfolio, with more than 50 products related to Corticosteroids, Hormones and Prostaglandins.

What will you do:

  • Writing and updating of EU-CTD (module 3.S);
  • Writing and updating of US DMT type II;
  • Writing and updating of J-DMF;
  • Writing and updating of documentation to obtain or maintain CoS (CEP) at EDQM;
  • Customer technical support;
  • Submission of regulatory documentation worldwide;
  • Regulatory management of changes;

Who I am looking for:

  • Strong multitasking skills, able to manage different project at the same time;
  • Ability or motivation to be in contact with Worldwide customers for regulatory technical support;
  • Fluent in English (knowledge of Portuguese is a Plus);
  • Dynamic, proactive and willing-to-do person;
  • Bachelor Degree in scientific environment;
  • 3 Years Experience as Regulatory Affairs (in API Production companies or Pharmaceutical groups) or as Quality Assurance; MOD CMC

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 niche markets we cover.

Posted: 14/05/2021 | NPJ Ref: 270702
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