CMC Specialist - Regulatory Affairs Professional

We are currently seeking a highly skilled professional to join our team as a Regulatory Affairs Specialist in the field of Chemistry, Manufacturing, and Controls (CMC). This position is located in a metropolitan area within a leading pharmaceutical company.

Key Responsibilities :

• Support the development of CMC strategies for various products to ensure globally approvable dossiers.
• Collaborate with cross-functional teams to ensure timely compilation of high-quality documents.
• Manage post-approval changes and product lifecycles.
• Drive continuous improvement initiatives.

Requirements :

Benefits :

We promote diversity and inclusion in our hiring process, ensuring that all candidates are considered equally, regardless of personal background or characteristics.

We encourage applicants to consider the environmental impact of their daily choices and strive to reduce our footprint through sustainable practices.