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27.01.2025
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Teva Senior Manager Medical Writing - Innovative Medicine R&D Eas... United States, Georgia, Macon
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....
Write and edit clinical regulatory documents, including submission summaries and other complex documents. Ensure that documents include the proper content and context (from a regulatory medical writing perspective)and clear and...
Learn the process of drug product development. Contribute to biologic drug product formulation development studies through the application of High Throughput Experimentation (HTE). Gain hands-on experience with dynamic light scattering...
During the 12 weeks program, you will gain in-depth insight into the Bioassays/Cell-based assays group within Analytical Development department. Supported by a mentor and experienced colleagues, you will be directly...
During this 12-week program, you will gain experience in projects and activities happening within the Global HEVO department. Supported by a mentor and experienced colleagues, you will be directly involved...
Leading and managing all quality activities in R&D, ensuring compliance with GLP, GCP, and CMC standards. Overseeing Quality Compliance processes and supporting Teva R&D development centers and suppliers. Ensuring inspection...
Visual Management implementation in additional QC PCTs (LTS, RM, Microbiology, Stability). Identification of proper candidates (raw materials) that can be added to the Raman ID program.Your experience and qualificationsEnrolled 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....
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