Sr Associate GRAAS Operations
Amgen(27 days ago)
About this role
Join a team partnering with Global Regulatory Affairs and CMC to advance regulatory processes and support global submissions and authentications. The role combines day-to-day onsite administrative duties with managing Certificate of Pharmaceutical Product (CPP) workflows and supporting project initiatives to meet regulatory timelines. You'll work across functions to maintain documentation, leverage digital tools, and ensure delivery of authenticated documents to international destinations.
Required Skills
- Regulatory Affairs
- Document Management
- Authentication Processes
- Project Management
- Stakeholder Engagement
- Veeva Vault
- Smartsheet
- SharePoint
- Communication
- Analytical Support
+2 more
Qualifications
- Master's degree
- Bachelor's degree
- High School Diploma / GED
About Amgen
amgen.comAmgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics.
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