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Associate Iii Complex Gx Regulatory Affairs jobs at Teva in India, Bengaluru
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Bengaluru
36 jobs found
Yesterday
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Teva Associate II Complex Gx Regulatory Affairs India, Karnataka, Bengaluru
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With moderate to minimal guidance, prepare, review, and compile new submissions, deficiency responses (IRs, DRLs, CRLs), and amendments using the "Right-First Time" approach. Work with their manager to support early...
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Yesterday
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Teva Manager Complex Gx Regulatory Affairs India, Karnataka, Bengaluru
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Independently support the preparation, review, and compilation of regulatory submissions (original applications, supplements, and responses) for sterile complex generic products. Support early FDA engagement to align on development strategy, reduce...
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Teva Associate II Complex Gx Regulatory Affairs India, Karnataka, Bengaluru
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The Associate II, Complex Gx, Regulatory Affairs is responsible for the preparation and submission of high-quality regulatory filings—both pre- and post-approval—for U.S. FDA-regulated inhalation, implant, ophthalmic, and drug-device combination complex...
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Teva Application Developer III- Data Support India, Karnataka, Bengaluru
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Partner with Sales and Marketing Incentive Compensation teams to support IC related activites. Analytical support of the design, implementation, evaluation, and reporting of incentive compensation reports, and results including development...
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Teva Project Mgr III - Cloud Migration India, Karnataka, Bengaluru
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7-8 years of experience in managing large-scale infrastructure projects, with a focus on Cloud Migration and Data Center Consolidation. Bachelor’s degree in Engineering, Computer Science, Business Administration, or a related...
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Teva Project Mgr III - Application Maintenance & Services AMS India, Karnataka, Bengaluru
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7–8 years in project management, with at least 5 years in AMS or transformation in large-scale environments. Familiarity with pharma regulations (GxP), AMS operating models, and regulated application landscapes....
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Teva Assoc Dir Regulatory Affairs India, Karnataka, Bengaluru
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Provide strategic leadership and oversight for regulatory submissions (original applications, supplements, and responses) for complex generic products, specifically semi-solids, transdermals, and nasal sprays. Drive early FDA engagement to align on...
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Description:Full job details
With moderate to minimal guidance, prepare, review, and compile new submissions, deficiency responses (IRs, DRLs, CRLs), and amendments using the "Right-First Time" approach. Work with their manager to support early...
These jobs might be a good fit
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