Regulatory Affairs Specialist

3 settimane fa


Milano, Lombardia, Italia Recordati A tempo pieno
Job Description

Recordati is seeking a highly skilled Regulatory Affairs Specialist to join its international team. As a key member of the Corporate Regulatory Affairs department, you will be responsible for the management of regulatory activities for medicinal products for human use.

Key Responsibilities:

  • Preparation, review, and submission of relevant documentation to regulatory authorities
  • Management of data and documentation in electronic systems
  • Cooperation with cross-functional teams to determine and manage timelines for regulatory filings
  • Participation in the management of core dossiers, including gap-analysis activities
  • Maintenance of relations with regulatory authorities and monitoring of legislation in force

Requirements:

  • Scientific degree in Regulatory Affairs
  • 4-5 years of experience in regulatory affairs within multinational pharmaceutical firms or international regulatory consulting companies
  • High level of autonomy and strong work ethic
  • Excellent communication and collaboration skills

About Recordati:

We are a global pharmaceutical force with over 4,300 employees, committed to creating a diverse environment and cultivating a culture of inclusion.

We strive to continually lead with our values and beliefs, enabling our employees to bring their whole selves to work and develop their potential.

We are proud to be an equal opportunity employer, recruiting, developing, and rewarding without regard to various factors.



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