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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...
Support process development, optimization, and scale-up of sterile and biologics manufacturing processes. Work collaboratively with internal teams to design robust manufacturing systems, ensuring they meet performance, scalability, and quality standards....
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...
How you’ll spend your dayFollowing is a list of some but not all responsibilities and specific tasks that will be assigned to the person in this role:⦁ Uses HR metrics...
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...
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...
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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