求人検索
この求人の 取扱い会社 |
マイケル・ペイジ・インターナショナル・ジャパン株式会社/Michael Page International Japan K.K. |
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企業名 | 会社名非公開 |
職種 |
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業種 | 製薬メーカー |
勤務地 |
アジア
日本
東京都
|
仕事内容 |
Be part of one of the top global pharmaceutical companies in the industry. Take lead in GQP QA activities to ensure effective compliance. Description * Ensure GQP Compliance: Oversee GQP Quality Assurance activities, ensuring alignment with policies, regulations, and global requirements. * Manage Quality Systems: Collaborate with manufacturing sites to implement and maintain effective quality systems and manage deviations, investigations, and change controls. * Support Regulatory Filings & Audits: Assist with regulatory filing updates, new product launches, and conduct routine GMP audits, addressing any gaps. * Conduct Due Diligence & Compliance: Perform quality assessments for new partners and ensure compliance with regulatory requirements, including pharmacopeia updates and new regulations. * Cross-Functional Collaboration: Work closely with various departments and external partners to support business development, regulatory inspections, and ensure stable product supply. Profile * University degree in scientific or related environnment * High fluency in English and Japanese * QA experience in the pharmaceutical industry * Strong understanding of GMP and GQP within GxPs Job Offer * Competitive salaries and benefits * Great work life balance * Hybrid working style * International environment * Amazing career progression in QA * Work with industry leaders who are solving various unmet needs Page Group Japan is acting as an Employment Agency in relation to this vacancy. |
企業について (社風など) |
* One of the top global companies in the industry * Rich development pipeline for unmet medical needs * Specializing in oncology, vaccines, infectious diseases, neuroscience, immunology etc. * Several blockbuster products * International working environment |
英語能力 | ビジネス会話 (TOEIC 735-860) |
日本語能力 | ネイティヴレベル |
年収 | 日本・円 800万円 〜 1000万円 |