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:

  • Final Batch release for the italian market on electronic system/interfaces with warehouse
  • Preparation and/or approval of technical agreements ensuring the application of GMP
  • Support the global QC for Audits
  • Complaints management
  • Internal training

He/she will develop the above activities with strong interaction with logistic-warehouse and international production plants.

Skills to cover the position:

  • Degree in scientific disciplines
  • Experience matured in multinational pharmaceutical and commercial companies.
  • Good knowledge og GMP rules
  • Good knowledge of IT tools, particularly Office, Oracle knowledge is a plus
  • Fluent knowledge of english language
  • Organizational skills, proactivity, ability to work in a team and determination to achieve objectives complete the profile

The company offers insertion 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: selezione3@hrexecutive.it specifying their consent to the processing of personal data (DL196/03) and ref.HR15 in the subject of the email.