・バイオ医薬品のGMP製造(治験薬、商用生産)に従事

・再生医療のCMC、プロセス開発を経験

・バイオ医薬のプラントエンジニアリングを経験

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Major classification

GMP, CMC

Middle classification

Biologics

Subcategory

detail

・responsible for cGMP manufacturing of biologics

・CMC and bioprocess development in cell therapy and regenerative medicine products

・Plant Engineering in biopharmaceutical manufacturing and validation support complying with cGMP regulation

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