Regulatory Affairs Specialist at Organon

Setup: Remote, Hybrid
Type: Full-time
Level: not_specified
Posted: Jul 27, 2026

Description

This role involves coordinating and supporting all regulatory activities to ensure the maintenance of marketing authorizations and obtaining new ones for the company's portfolio under various EU procedures. It requires strong project management skills to oversee regulatory initiatives, manage timelines, and facilitate collaboration within cross-functional teams.

Required Skills

Regulatory Information Management Systems
Veeva
Ennov
Power BI

Additional Information

Required Previous Experiences: 5+ years of experience in the pharmaceutical industry or a comparable field, with extensive involvement in registration processes across multiple European markets and practical expertise in managing European regulatory procedures.
Preferred Qualifications: Fluent in written and spoken English, with proficiency in at least one additional European language.
Strong verbal and written communication skills, along with excellent organizational and planning abilities.
Meticulous attention to detail and adaptability to manage conflicting deadlines and high workloads.
Mature and professional approach to work, with a clear understanding of the commercial significance of the role.
Ability to collaborate with colleagues across all levels and functions, both within Europe and internationally, with potential to take on leadership responsibilities.
Capable of working independently and as part of a team across a wide geographic scope.