AbbVie is seeking a Regulatory Affairs professional to support end-to-end regulatory submissions and lifecycle management for products in the portfolio. You will coordinate with cross-functional teams and regulatory authorities to ensure timely and compliant filings.
The role requires 2–3 years in Regulatory Affairs, English proficiency at least B1-B2, and a Pharmacy-related degree. Collaboration with Medical, Commercial, and Quality teams is essential to minimize risks and ensure patient access.