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We are seeking a dedicated Regulatory Affairs Professional to join our growing team. This role offers an opportunity to work with global and local regulatory teams, supporting product lifecycle management and ensuring compliance with health authority requirements. The role can be home or office based in various European locations.

Role Responsibilities:

Support global and/or local regulatory teams with comprehensive understanding of regional and global regulatory requirements

Manage post-authorization lifecycle maintenance procedures (variations, renewals, PSURs) for multiple licenses

Coordinate health authority interactions and responses to questions

Prepare and organize local-specific documentation (Module 1) to meet national submission requirements

Maintain up-to-date local national systems according to local legislation

Manage impact assessments for technical changes affecting marketing authorizations

Stay current on regulatory requirements and guidelines to ensure compliance

Support health authority inspections as needed

Provide technical and business consulting services within area of expertise

Complete activities within project scope, timeline, and objectives

Skills and Experience required for the role:

University Degree in a Scientific or Technical Discipline

A few years of experience in an industry-related environment

Experience in regulatory authority-facing roles

Regulatory Operations (Submission management) experience

Experience using Veeva Vault RIMS - strong plus

Outstanding interpersonal and intercultural communication skills (written and verbal)

Critical thinking and problem-solving abilities

Fluent in English, written and spoken