Regulatory Affairs Associate - Eu Generics jobs at Teva in United Kingdom
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9 jobs found
13.07.2024
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Teva Regulatory Affairs Associate - EU Generics United Kingdom, England
Ensure dossier technical content is optimal and aligned with EU Regulatory data requirements for new EU Marketing Authorisation Applications and post approval variations, where required. Perform the necessary regulatory activities...
You will (with support from Line Manager) prepare, compile, review and submit appropriate high quality post-approval changes (variations, renewals, PIQU submissions) and responses to Health Authority questions in accordance with...
Provide accurate and timely device specific regulatory guidance to teams engaged in the development and lifecycle of drug device combination products and devices by assessing and interpreting global regulatory guidance’s...
You will develop regulatory strategies during development, approval and post approval phases for submissions to EU Competent Authorities. You may also have the opportunity to do this on a Global...
Managing complex, high value pan-European pharmaceutical patent and regulatory exclusivity litigation strategies to advance Teva’s commercial objectives. Working with cross-functional teams within Patents, EU Legal, Portfolio, Commercial and Regulatory Affairs...
You will manage, lead and motivate a successful high performing team in a fast-paced environment, including budgetary responsibility for medical cost centres. You will develop long term strategy, lead agile...
You will provide leadership and support to Teva UK Limited and Teva ROI cross functional teams to ensure new product launch readiness. You will be able to lead and motivate...
Ensure dossier technical content is optimal and aligned with EU Regulatory data requirements for new EU Marketing Authorisation Applications and post approval variations, where required. Perform the necessary regulatory activities...
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