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 |
メディカル/医薬/バイオ/素材/食品 - 品質管理/保証
メディカル/医薬/バイオ/素材/食品 - 臨床開発系 |
業種 | 医療・福祉関連 |
勤務地 |
アジア
日本
東京都
|
仕事内容 |
Reporting APAC in a stand alone position. Be a key member in clinical quality management to ensure effective compliance. Description * Supporting clinical quality management including ICH GCP, clinical regulations/requirements, data management of clinical trials * CSV * Supporting clinical trial processes including eTMF, TMF, SMF * Operate in quality incident management, internal quality system audits, customer audit/inspection Profile * University degree in scientific or related field * High fluency in English and Japanese (non-native level speakers will not be selected) * Clinical quality experience with strong understanding of ICH GCP ideally in the pharmaceutical industry * CSV experience * Exposure to quality systems processes including auditing, root cause analysis, and CAPA development * PMDA inspection experience is preferred * Ability to work independently Job Offer * Competitive salaries and benefits * Great work life balance * International working environment * Hybrid working environment * Work with industry leaders who are solving unmet needs * Great career progression Page Group Japan is acting as an Employment Agency in relation to this vacancy. |
企業について (社風など) |
* Global healthcare technology company specialising in digitisation for clinical trials * Supporting over 30,000 clinical trials around globe * International working environment with extensive global collaboration * Hybrid working style |
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 1200万円 〜 1400万円 |