Regulatory Affairs Associate I - West Chester
2 weeks ago

Job summary
We're Teva, a leading innovative biopharmaceutical company.Here, you will be part of a high-performing,
inclusive culture that values fresh thinking and collaboration.
You'll have the room to grow,
the flexibility to balance life with work,
and the opportunity to better health worldwide,together.
- Publish and dispatch major and complex routine/lifecycle management eCTD submission projects
- Collaborate with scientific personnel for planning preparation publishing and quality control checks of submissions.
Job description
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