Our customer is a Multinational company leader in the production and distribution of equivalent drugs (ethical and hospital) and consumer products , we have been charged to recruit for the italian branch  active in the distribution of its products to the Pharmacies and Hospitals channel, the following professional figure:


 The position will be inserted in the Regulatory Affairs team and reporting to the Regulatory, Pharmacovigilance and Quality Manager will take care of the following activities:

  • Preparation and submission of marketing authorization applications (national procedures)
  • Preparation and management of activities related to requests for changes / renewals through MRP / DCP procedures
  • Preparation of technical documentation to support type I, II changes, renewal and MAH transfers
  • technical writing of the quality of Module 3
  • management and updating of product information
  • publication in the Official Journal
  • database maintenance

Skills to cover the position:

  • Degree in technical scientific disciplines (Pharmacy, CTF, Biology, Chemistry)
  • Previous experience in a similar position matured in companies in the pharmaceutical sector
  • Good knowledge of IT tools, particularly Office
  • Fluent knowledge of english language
  • Problem solving and result orientation; team working and adaptability; analytical skills, precision and punctuality

The company offers hiring with a permanent contract in an international and growing context.

Job site: North- West Milan

To apply to the offer, we invite interested people (L.903/77) to send their detailed curriculum to: specifying their consent to the processing of personal data (DL196/03) and ref.HR22 in the subject of the email.

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