When our values align, there's no limit to what we can achieve. We are looking for a Senior Regulatory Affairs Manager/Consultant with 10+ years of experience in regulatory affairs, including CMC expertise.

This challenging role offers the opportunity to work on diverse projects, manage client relationships, and contribute to regulatory strategies in a global pharmaceutical environment.

This is a client dedicated project, without people management responsibility.

The role can be home or office based in various European locations.

Key Responsibilities: Write CMC sections (23 S, 23 P, 32 S, 32 P) and scientific rationales for regulatory submissions and responses Develop and implement variations strategies based on EU guidelines Coordinate CMC activities across multiple projects Liaise with global affiliates and manufacturing sites Provide project leadership and management Ensure client satisfaction and project quality Identify new business opportunities and contribute to proposal preparation Required Qualifications:10+ years of experience in regulatory affairs Extensive knowledge of CMC writing and variations strategy In-depth understanding of EU guidelines (Variation, ICH, EMA)Excellent project management and organizational skills Strong communication abilities and client management experience Ability to work independently and as part of a team Proficiency in English; additional languages are a plus Preferred Qualifications: Experience with regulatory agencies (e.g., FDA, MHRA)Industry-recognized certifications or advanced degrees Publication history or experience presenting at industry conferences