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 - 薬事申請/特許技術関連 |
業種 | 製薬メーカー |
勤務地 |
アジア
日本
東京都
|
仕事内容 |
Take lead in the company starting up for their market entry to Japan. Take lead in the overall RA activities to obtain regulatory approval. Description * Take lead in the establishment of the RA organization * Develop effective regulatory strategies to obtain product approval * Communicate with global stakeholders to develop regulatory plan * Discuss, negotiate, develop key relationships with local health authorities (PMDA) * Educate the business on local regulations Profile * University degree in scientific or related area * High level English and Japanese (non-native level speakers will not be selected) * Extensive RA experience in the pharmaceutical industry * Ability to work independently in a fast-growing start-up environment * Strong knowledge of local regulations and track record of product approval Job Offer * Competitive salaries and benefits * Great work life balance * Be part of the company's market entry to Japan * Develop the RA department * Work with industry leaders who are solving various unmet medical needs * Amazing career progression in RA To apply online please click the 'Apply' button below. For a confidential discussion about this role please contact Saki Kanematsu at +81 3 6832 8904. |
企業について (社風など) |
* Global pharmaceutical company specialising in oncology, autoimmune diseases, and ophthalmic diseases * Patient-centric business delivering various unmet medical needs * International working environment with extensive collaboration with stakeholders around the globe * Planning to enter the Japan market to target for various patients |
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 1400万円 〜 2000万円 |