Senior Regulatory Affairs Specialist jobs in Newark, DE
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SENIOR DIRECTOR, REGULATORY AFFAIRS CMC , INNOVATIVE MEDICINE (HYBRID)
Influence the strategy and assess the quality of documents for regulatory submissions to major market health authorities as well as coordinate with global regulatory colleagues to prepare dossiers for global registration.. Ident...
| Company | Teva Pharmaceuticals |
|---|---|
| Address | West Chester, PA |
| Category | Information Technology |
| Date Posted | 2 months ago See detail |
Senior Director, Regulatory Affairs CMC , Innovative Medicine (Hybrid)
Teva Pharmaceuticals
West Chester, PA
Influence the strategy and assess the quality of documents for regulatory submissions to major market health authorities as well as coordinate with global regulatory colleagues to prepare dossiers for global registration.. Ident...
2 months ago seen See more...
Senior Director, Regulatory Affairs II
Teva Pharmaceuticals
West Chester, PA
Manage resources to support submission activities for responsible sites and oversees the coordination and delivery of major submissions to directly support the companies growth strategy. Build relationships with RA staff/authorin...
2 months ago seen See more...
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