Global Regulatory Affairs Lead (CMC and Development

We are looking for an experienced individual in Global CMC (Chemistry, Manufacturing, and Controls) Regulatory Affairs to join a dynamic team. The role will be responsible for leading regulatory strategy and submissions for innovative biopharmaceutical products.

Requirements

• Scientific degree or any related discipline
• Strong professional working experience in global CMC regulatory strategy leading activities
• Knowledge of the interdisciplinary functions involved in CMC drug development and the application of clinical research to drug development
• Combination of strategic and operational skills

Benefits

• Competitive salary, including attractive packages
• Remote working opportunity
• Excellent company culture
• Exposure to a dynamic and evolving Biotech company