Global CMC Regulatory Lead: Combination Products

A leading biopharmaceutical company in Dublin is looking for an Associate Director in CMC Regulatory Affairs to lead regulatory strategies for combination products. This role involves mentoring staff, engaging with regulatory authorities, and ensuring compliance for clinical and commercial filings. Candidates should have extensive experience in regulatory affairs, strong problem-solving skills, and the ability to communicate effectively across teams. An inclusive company culture with comprehensive benefits is offered, promoting collaboration and efficiency in the workplace.