What you’d do
Plans and executes US regulatory strategies for assigned Amgen products, managing local regulatory submissions, developing and maintaining local labels, and advising on mechanisms to optimize approvals. Full time, remote within the United States. Found on the employer's careers page on Oct 18, 2026. Apply through the link.
You’ll need
- Understanding of drug development
- Knowledge of regulatory principles
- Regulatory submissions experience
- Experience interacting with regulatory agencies (FDA)
- Working knowledge of US legislation/regulations for medicinal products
Our summary of the listing. The full listing has the details.