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06.04.2025
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Teva Manager Regulatory Affairs United States, New Jersey
Prepare, review and approve regulatory submissions (i.e. ANDAs, amendments, supplements, etc.) to the Food and Drug Administration (FDA) to ensure compliance with applicable regulations and guidance. Prioritize many projects including...
Develop Business Relationships: Create effective relationships with business stakeholders to ensure expectation management and alignment of team priorities with the business. Create Value: Work with the business and IT management...
Comprehensive Health Insurance: Medical, Dental, Vision, and Prescription coverage starting on the first day of employment, providing the employee enrolls. Retirement Savings: 401(k) with employer match, up to 6% and...
The Director Commercial Quality US is the Quality Business Partner to the Commercial US Teams and is the coordinator for critical quality incidents impact drug supply continuity. Develops and sustains...
Draft, negotiate and review contracts, including license agreements, product development agreements, technology service agreements, distribution agreements, consulting agreements, engagement letters, confidentiality agreements and other business and legal documents. Advise BD...
Develop clear, accurate, high-quality internal and external scientific-medical-technology content for internet and intranet, social media, organizational communications and external press materials based on defined scientific communications strategy from Teva. In...
Focus on product and program-level responsibilities, providing leadership and accountability for key regulatory documents. Potentially oversee direct reports, contingent workers, and/or vendors, while also offering training and resource management support....
Prepare, review and approve regulatory submissions (i.e. ANDAs, amendments, supplements, etc.) to the Food and Drug Administration (FDA) to ensure compliance with applicable regulations and guidance. Prioritize many projects including...
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