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Director Regulatory Affairs Cmc Combination Products jobs at Teva in United Kingdom
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25 jobs found
12.04.2025
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Teva Senior Director Global MS & Sterile Biopharmaceutical Produc... United Kingdom, England
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Experience:o Minimum of 10 years of experience in Manufacturing Science and Technology, with a strong focus on sterile products (injectables, biologics, etc.) in a GMP environment.o Proven expertise in biopharmaceutical...
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24.03.2025
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Teva Corporate Affairs Lead United Kingdom, England, Wakefield
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You will develop and execute internal and external corporate communication and engagement strategies and plans, aligned with our global and regional priorities. You will serve as the communications business partner...
17.03.2025
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Teva Associate Director Customer Excellence United Kingdom, England, Wakefield
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You will be partnering with the business to define key customer groups, aligned to product requirements and our overall commercial strategy, and will define our value proposition and strategic imperatives...
16.03.2025
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Teva Associate Director Corporate Affairs United Kingdom, England, Wakefield
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You will develop and execute internal and external corporate communication and engagement strategies and plans, aligned with our global and regional priorities. You will serve as the communications business partner...
04.03.2025
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Teva Director Pipeline Immunology Asset Lead Global United Kingdom, England
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Developing GHEVO Strategies:Lead the creation and implementation of evidence generation plans to support the value proposition of pipeline immunology assets, ensuring alignment with regulatory and governance standards. Provide insights into...
27.01.2025
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Teva Product Pipeline Manager - Associate Director United Kingdom, England, Wakefield
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You will manage Teva’s pipeline of generics and biosimilars, from initial concept through to commercialization. Lead the coordination of product development across cross-functional teams, ensuring a seamless transition from early-stage...
20.01.2025
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Teva Director Global Pharmacovigilance - Safety Physician United Kingdom, England
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Lead the safety profile of the assigned product(s) during clinical development including Company Sponsored studies, Investigator Sponsored studies, Compassionate Use and Disease Monitoring Programs. Collaborate with other R&D teams to...
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Description:Full job details
Experience:o Minimum of 10 years of experience in Manufacturing Science and Technology, with a strong focus on sterile products (injectables, biologics, etc.) in a GMP environment.o Proven expertise in biopharmaceutical...
These jobs might be a good fit
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