Regulatory Affair Specialist jobs in Chester, PA
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DIRECTOR REGULATORY AFFAIRS - SUBMISSION MANAGEMENT - WEST CHESTER, PA
Responsible to manage Product Submission Team and dossier timelines. Accountable to Global Regulatory Lead and Global Regulatory Affairs, with matrixed accountability to Project Management. Regularly reports to management on progr...
| Company | Teva Pharmaceuticals |
|---|---|
| Address | West Chester, PA |
| Category | Information Technology |
| Date Posted | 3 days ago See detail |
Director Regulatory Affairs - Submission Management - West Chester, PA
Teva Pharmaceuticals
West Chester, PA
Responsible to manage Product Submission Team and dossier timelines. Accountable to Global Regulatory Lead and Global Regulatory Affairs, with matrixed accountability to Project Management. Regularly reports to management on progr...
3 days ago seen See more...
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...
3 weeks ago seen See more...
Manager, CMC Regulatory Affairs - West Chester, PA
Teva Pharmaceuticals
West Chester,
Provide CMC regulatory guidance to teams engaged in the development of new products by assessing and interpreting FDA/ICH/EMEA regulatory guidance and directives, and evaluating and communicating their applicability to the develop...
3 weeks ago seen See more...
- View all Teva Pharmaceuticals jobs - jobs in West Chester,
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...
3 weeks ago seen See more...
Manager, Regulatory Affairs - Biosimilars
Teva Pharmaceuticals
West Chester, PA
The Manager is responsible for supporting the Regulatory Affairs strategic vision and regulatory leadership in defining the global regulatory strategy for biosimilar projects. The Manager is accountable to support the Global Regul...
a month ago seen See more...
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