About this role
The RA Specialist at Sandoz supports regulatory affairs functions for drug product registration, focusing on management of registration data and FDA submissions. This independent-contributor role acts as a systems and process subject-matter expert, collaborating across stakeholders to support harmonization and lifecycle management. The position is based at Sandoz's Princeton, NJ headquarters with a hybrid work arrangement.
Required Skills
- Analytical
- Clinical Trials
- Collaboration
- Detail Oriented
- Life Sciences
- Project Planning
- Regulatory Compliance
- Data Management
- Submissions
- Communication
+2 more
Qualifications
- Associate Degree in Information Management Systems
- Bachelor's Degree in Information Management Systems
- Master's Degree Preferred
About Sandoz
sandoz.comSandoz is the global leader in generic and biosimilar medicines. Our Purpose is to pioneer access to medicines for patients globally.
View more jobs at Sandoz →Apply instantly with AI
Let ApplyBlast auto-apply to jobs like this for you. Save hours on applications and land your dream job faster.
More jobs at Sandoz
Similar Jobs
Senior QA/RA Specialist
Aegis Ventures(1 month ago)
RA Specialist
Ortho Clinical Diagnostics(1 month ago)
Associate - Regulatory Affairs (Publishing)
ClinChoice(6 days ago)
Manager, Regulatory Delivery Excellence, China Regulatory Affairs
LI Test Company(2 months ago)
RA Manager
Abbott Laboratories(2 months ago)
Manager, Regulatory, International Markets (MENA) (1 year contract)
BridgeBio Pharma(2 months ago)