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Takeda Pharmaceuticals
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Zurich,
Switzerland
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years of pharmaceutical industry experience, with a minimum of 6 years of regulatory experience.
European regulatory experience is essential. Preferred experience in managing filings to EMA via
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Takeda Pharmaceuticals
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Zurich,
Switzerland
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Engineering Discipline.
8+ years of pharmaceutical Regulatory CMC and Medical Device experience, including experience as a regulatory representative for drug-device combination products in EU & Global
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Takeda Pharmaceuticals
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Zurich,
Switzerland
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experience, including experience as a regulatory representative for drug-device combination products
Experience working on cross-functional submission teams
Solid understanding and proven ability to
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Takeda Pharmaceuticals
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Zurich,
Switzerland
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role:**
Join Takeda as the International Head (Executive Director) for the Global Regulatory ... within the department and cross-functionally.· Uses your experience to oversee the strategic
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Takeda Pharmaceuticals
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Zurich,
Switzerland
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minimum of 15 years of regulatory affairs experience in the pharmaceutical/biotechnology industry within ... products.
Experience with advanced therapeutic medical products (Cell & gene therapy) will be
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