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Director, Regulatory Affairs
2 months ago
Unlock Your Potential in CMC Regulatory Affairs
Are you a seasoned expert in Chemistry, Manufacturing, and Controls (CMC) with a passion for driving high-quality regulatory submissions? We're looking for a dynamic leader to steer multi-modality projects from development to commercialisation.
Key Responsibilities:
Lead the preparation and submission of CMC packages for both small and large molecules.
Collaborate across Tech Ops, Global Regulatory Affairs, and Quality teams to ensure timely, high-quality deliverables.
Manage and mentor a high-performing team, ensuring alignment with global regulatory standards.
Why Join Us?
Be at the forefront of innovation in rare disease treatments.
Work in a fast-paced, patient-focused environment.
Grow your career with opportunities to lead and make a global impact.
If you’re ready to take your CMC expertise to the next level, we want to hear from you Let's transform lives together.
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