Job Purpose

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We are looking for a Regulatory Affairs Associate – Fixed‑term contract to join the International Corporate Regulatory Affairs team, responsible for managing regulatory activities for SPC medicinal products for human use. Responsibilities include obtaining and maintaining marketing authorisations in the European Union (through CP/MRP/DCP) as well as supporting regulatory activities in various non‑EU regions, including Africa, Asia Pacific, CENAM, CSI, LATAM, MENA.

Key Responsibilities
The candidate will be responsible for the preparation, review and submission of regulatory documentation to Health Authorities, as well as for the management of regulatory data and documentation within relevant electronic systems, in support of:

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- New Marketing Authorisation Applications
- Line‑extension
- Renewal of Marketing Authorisations
- Variations Type IA, IB, II (including grouping and worksharing procedures)



or equivalent procedures in accordance with national legislation
- Marketing Authorization transfers
- Notification of start and end of marketing
- Requests for Sunset Clause exemptions
- Review and approval of printed materials (artworks and mock‑ups)

Based on the products assigned, the Regulatory Affairs Associate will also:

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- Define regulatory activity plans and related costs
- Collaborate with cross‑functional teams to define and manage timelines for the preparation of regulatory submissions
- Contribute to the management of core dossiers, including gap analysis activities, to support registrations across multiple international markets, in collaboration with relevant departments
- Coordinate with the group's affiliates, licensees and consultancy companies
- Maintain relations with the Regulatory Authorities
- Monitor the legislation in force and assure the regulatory compliance
- Provide regulatory assessment for new business

📌 Regulatory AffaiRegulatory Affairs Associate (Turbigo)
🏢 Recordati
📍 Turbigo