Our client, a group of companies dedicated to researching, developing, manufacturing and marketing pharmaceuticals that improve health and quality of life is seeking a Group Manager for their office in Hyogo. The Group Manager will be responsible for developing state of the art analytical methods (e.g., HPLC, GC) and conduct stability studies for new drug products in accordance to all applicable guidelines and regulations (ICH, cGMP, SOPs, etc.) ・ Method development for new NCEs based on their phys. - chem. properties ・ Maintains and newly establish state of the art technology ・ Supports Pharmaceutical Research developing trial and final formulations ・ Designs and execute ICH and cGMP compliant stability studies applying newly developed analytical methods ・ Determines long-term stability and shelf-life of new drug products ・ Provides guidance to PHR wrt viable formulation approaches ・ Compiles stability reports ・ Summarizes all results and present all relevant data to the international R&D team ・ Communicates and implement all team decisions within the department (matrix management function) ・ Communicates and resolve conflict ・ Plans, prepares and conducts method transfers ・ Trains analytical staff and report results ・ Prepares submission documents for J-NDA and global MAA submissions ・ Interacts with DRA and CMC Experts on content and format of documentation ・ Contributes to establish proactive response strategies ・ Interacts with international regulatory bodies during the development (e.g, pre-NDA meetings, formal and informal discussions, etc.), submission, review and post marketing phase ・ Supports operations in performing quality investigations ・ Trouble shooting and problem solving for commercial products ・ Interacts with partners and customers ・ Coaches staff to acquire skills, help them to solve problems and develop their career plans ・ Provides staff with career development opportunities on-the-job and also off-the-job ・ Leads by example

・主に感染症関連製品の学術を担当 ・評価治験のプロトコル作成 ・評価治験の実行とまとめ ・学術資料の作成 ・ＫＯＬへの製品説明 ・拡販目的の学術講演 ・営業・卸等販売チャンネルへの教育 ・本社学術とのコミュニケーション ・セミナーの企画と実行

・免疫検査領域の製品を担当 ・長期計画、次年度予算および販売予測の作成 ・マーケティングプランの作成と実行 ・新製品の上市計画の作成と実行 ・販促物の企画および製作 ・市場調査、ＫＯＬインタビューおよび競合調査 ・本社および地域マーケティングとのコミュニケーション ・学会展示およびセミナーの企画と実行　　

グローバルネットワークを持つ外資系企業での、購買・調達業務 募集背景： * 組織力強化の為 会社概要: * 医療用医薬品、動物用医薬品、農薬の製造・販売・輸出入 仕事内容： *医薬品の製造に使用される原料と資材に関する購買業務全般 *業者の評価・選定、価格交渉、契約・発注、納期管理など *国内外の調達の最適化及び業務プロセスの改善 *関係部署（品質部門や製造部門など）と協力して、変化に機敏に対応する 年収： * 500～700万円、スキル・経験により異なる 活かせる経験： *購買・調達の実務経験 *英語力 *医薬品業界の知識・経験 求める人物像： *行動力・協調性があり、周囲に良い影響力のある方 *リーダーシップを発揮できる方 *優れた対人能力・交渉力を有する方

外資系医薬品メーカーがパッケージデザイン経験者を探しています。 関連部署と連携して、各種要件（関連法規・社内ガイドライン遵守、医療事故防止等）を満たしたパッケージをデザインし、仕様を設計していただきます。また、ビジネス部門や顧客の要望も取り入れ、顧客満足を反映させたデザインや仕様案も提案していただきます。 ・医薬品のPTP・個装箱・ラベル・段ボール等の包装デザイン、仕様の設計・製作 ・包装情報の管理 ・包材ベンダー窓口としての業務管理

One of the world leading Pharmaceutical companies are seeking Assistant Product Managers and marketing managers. The company has a strong pipeline for Oncology, CNS, Respiratory and Vaccines. The company will launch several blockbuster products in the next 3 years. Responsibilities: To developing marketing strategies for new products. To increase sales and market share. To provide medical representatives with a clear marketing message

- Report to Head of Quality Assurance - Plan audit schedule for clinical trials. - Conduct audit (for healthcare providers, CROs, internal process 　　and documents) - Conduct training and consultation for non-QA departments. - Review SOP, WI and checklists related to QA.

Leading OTC company in Japan is seeking a Brand Manager. Job Purpose: Planning and implementation of brand marketing strategies in order to keep increasing the sales and market share as well as to increase the current profits. Job Responsibilities: 1.Plan and suggest the 3-year Plan and acquire approval Analyze phenomena and data in order to get a grip of consumers’ tendencies and brand category trends. Based on the above analysis, plan brand positioning and main strategies. Confirmation of consistency between strategies and implementation plans (including budgets and long-term targets). 2.Implementation of annually approved marketing plans Adjusting of sales forecast, manufacturing, and supply of products in order to efficiently maintain the inventory. Securing and implementing of brand advertising in magazines and sales promotion budgets. To differentiate from competing firms and to establish long-term brand identity, create strong creative. give suggestions to the sales staff who are involved in marketing planning, and make sure to provide them with supporting materials when necessary. Actively utilize the global new products development projects for sustainable growth, and maximize the pipeline. In order to solve unexpected issues as well as to grab the right timing/chances, update and revise plans. 3.Give ideas that are beyond the plans and take action Contribute to maximize the profitability of the products. Have coherent understanding of the products, consumers, competition, and regulations, and create a flow of leading-edge ideas that are beyond the plans.

仕事内容///////////// 企業法務全般。特に契約書(海外契約含む)の作成、審査、相談等。 会社概要/////////// 1963年の創業以来、「私たちは 人びとの健康を高め 心豊かな社会づくりに貢献します」の企業理念のもと、独創的な医薬品の研究・開発に取り組んでまいりました。医療用医薬品におきましては、抗悪性腫瘍剤「ユーエフティ」、「ティーエスワンカプセル」など、日本を代表する抗がん剤を世に送り出し、国内外から高い評価をいただいております。がん領域以外におきましても、尿失禁・頻尿治療剤「バップフォー錠」、アレルギー性疾患治療剤「アイピーディ」など、生活の質の向上に貢献できる製品を上市してまいりました。また、ヘルスケア商品におきましては、滋養強壮剤「チオビタ・ドリンク」、生薬配合剤「ソルマック」を始めとした健康維持・増進にかかわる商品に加え、生薬製剤/軽い尿もれ・頻尿用薬「ハルンケア内服液」のように、高齢化社会に強く求められる生活改善薬として、QOL（生活の質）の向上に貢献できる商品もお届けしております。　　　　

With operations in nearly all 50 US states, our client is one of the largest providers of pharmacy and related services to long term care facilities in the US. Currently employing over 15,000 people worldwide. The Tokyo office is expanding rapidly and this role would incorporate a lot travel throughout the APAC area coordinating and monitoring clinical trials. Responsibility : Responsible for the day-to-day management of the statistical activities of the Biostatistics department. . Coordinate and/or conduct and/or participate, or manage, in any or all assigned biostatistical activities for the design, implementation, data summarization/statistical analysis and reporting of clinical trials