Senior Director CMC Regulatory Affairs

Finding the ‘Needle in the Chaystack’ Talent#Regulatory Affairs

Responsibilities:

• Lead global CMC regulatory strategy for commercial biologic products, focusing on post-approval changes, lifecycle management, and dossier maintenance.
• Prepare and deliver high-quality CMC documentation for global submissions (e.g., supplements, variations, amendments) supporting manufacturing process changes, analytical method updates, site changes, and supplier modifications.
• Provide strategic guidance to cross‑functional teams based on strong understanding of biologics manufacturing, control strategies, comparability principles, and process validation requirements.
• Support data review and regulatory readiness for manufacturing/technical changes, including comparability assessments and process improvements.
• Develop responses to Health Authority questions and contribute to briefing materials for global agency interactions.
• Maintain compliance with global regulations and guidelines (FDA, EMA, ICH Q5–Q12) and monitor evolving regulatory expectations for biologics.
• Collaborate with Technical Operations, Quality, Process Development, and Supply Chain to align regulatory strategies with business and technical priorities.

Qualifications:

• Bachelor’s degree in a relevant scientific field (advanced degree preferred).
• Approximately 8 years of Regulatory CMC or related experience supporting biologic drug products.
• Strong working knowledge of biologics manufacturing, analytical methods, control strategies, and post-approved regulatory requirements.
• Proven experience preparing and submitting global post‑market CMC changes for biologics (US, EU, and international regions).
• Ability to lead regulatory strategy, influence cross‑functional stakeholders, and manage multiple global projects.
• Excellent communication, technical writing, and organizational skills.

• Director

• Full-time

• Science

• Pharmaceutical Manufacturing and Biotechnology Research