Regulatory Affairs Associate I - West Chester

Only for registered members West Chester, United States

2 weeks ago

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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.

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