 
						Associate Director Regulatory Affairs
1 week ago
An innovative and purpose-driven biotechnology, biologics company is seeking a Regulatory Affairs Associate Director to join its growing team. This role will be instrumental in shaping and executing global regulatory strategies, supporting clinical development across oncology and autoimmune programs. As a senior individual contributor, the Regulatory Affairs Associate Director will bring deep regulatory expertise, particularly in the Asia-Pacific market, and a strong ability to collaborate across Clinical, CMC, and Safety functions. The Regulatory Affairs Associate Director will play a hands‑on role in managing IND and CTA submissions, supporting regulatory designations such as Fast Track and Orphan Drug, and overseeing vendor relationships. This position requires someone who can think strategically while staying grounded in the operational execution needed to advance complex development programs. Adaptability, clear communication, and a proactive mindset are essential to thrive in this fast‑paced, evolving environment. Grounded in a culture of excellence, integrity, and collaboration, the company offers more than a job, it offers purpose. As a Regulatory Affairs Associate Director, you will be part of a mission‑driven team that values continuous learning, flexible working arrangements, and the opportunity to contribute meaningfully to the development of transformative therapies. Do apply now for a confidential discussion. CEI: R | Licence No.: 22S1313 Seniority level Director Employment type Full‑time Job function Science #J-18808-Ljbffr
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