Jobs list of Pharmaceutical & Research & Development
-
NEWJob number: Job-00248738 Posted: 2023-05-26
海外製薬工場の管理
医薬品の生産に関する知識・経験をお持ちの方必見です。5 - 8 million yen Tokyo Pharmaceutical Research & Development
- Company overview
- Our client is a pharmaceutical company.
- Responsibilities
- 本社から海外工場を管理いただきます。管理指標から生産活動をモニタリング
品質改善や生産性向上など海外工場への技術支援
事業変化に応じた生産体制の再編
Patrick Chang
Pharma -
NEWJob number: Job-00248758 Posted: 2023-05-26
工場責任者
語学力を活かしてグローバルに活躍7 - 9.5 million yen Tokyo Pharmaceutical Research & Development
- Company overview
- Our client is a pharmaceutical company.
- Responsibilities
- 海外の医薬品工場における運営の責任者または準責任者候補としてご活躍。
工場管理全般
医薬品GMPの準拠（製造管理、品質管理の指導）
品質向上、コスト低減、安定供給の課題対応
投資管理、エンジニアリング業務
Patrick Chang
Pharma -
NEWJob number: Job-00248158 Posted: 2023-05-26
医薬品探索研究職
グローバルに活躍5.93 - 9.78 million yen Other Pharmaceutical Research & Development
- Company overview
- Our client is in the pharmaceutical firm.
- Responsibilities
- 蛋白質の機能解析、構造解析研究(X線結晶構造解析、CryoEM)を中心とした医薬品探索
蛋白質発現、精製、構造解析、化合物との相互作用解析手法の立案および試験の実施
構造解析や相互作用解析を中心とした新規創薬技術の調査、検討、立案
Patrick Chang
Pharma -
NEWJob number: Job-00228583 Posted: 2023-05-25
Health Outcomes Scientist/RWE Tokyo
Rich pipeline6 - 14 million yen Kansai Pharmaceutical Research & Development
- Company overview
- Our client is one of the top medicine and Clinical Research companies worldwide.
- Responsibilities
- Provide scientific expertise and effective project oversight to ensure the success of the health outcomes (HO) research that are valued by payers and providers.
Projects may span the entire lifecycle of development and commercialization.
The Scientist develops HO research strategies to support Pricing, Reimbursement and Access activities for products.
Working with GPORWE and local functions, the Scientist is responsible for the conduct, quality, and integrity of HO studies and scientific disclosures and applies necessary knowledge, understanding, and evaluation of clinical, economic, and/or patient reported outcomes methodologies.
Emely Motol
Pharma -
NEWJob number: Job-00230224 Posted: 2023-05-24
Director Product Development
Leading CMO14 - 18 million yen Tokyo Pharmaceutical Research & Development
- Company overview
- Our client is a contract manufacturer of soft capsules for pharmaceuticals and health foods.
- Responsibilities
- Provide leadership and overall management responsibility for the local Product Development Team, which generally includes Formulation Development, Process Development, and Analytical Development.
Build and lead a high-performing Product Development Team. Attract and retain high-caliber talent, maintain clear roles and responsibilities, and determine development requirements for the team members.
Provide leadership in building and maintaining a robust pipeline of new products and technologies, and assist with project proposals to determine technical requirements, timing, funding, and procedures for successful completion of projects.
Ensure clear prioritization and execution of all projects in accordance with customer expectations in terms of milestone deliverables and budget.
Manage the execution of the overall portfolio of R&D projects, including customer development projects and Proactive Development programs.
Conduct regular Project Review meetings to assess product development plans and make adjustments as necessary to keep projects on track in terms of technical and quality deliverables, timelines, and budget.
Ensure complete documentation of product development program in accordance with appropriate quality and regulatory requirements.
Provide technical guidance with issues that focus on root cause identification and actions that improve our technical success.
Provide regular progress reports to management and stakeholders.
Responsible for meeting financial targets for development revenue and base cost.
Responsible for budget and resource planning and management, including determination of staffing requirements, and allotment of available resources to various stages of the projects.
Assist in development of improvement programs that instill a high-performing culture.
Participate in the design and implementation of standard policies and processes.
Interact with functional leaders along with other sites to ensure alignment on process and procedures.
Represent the product development team in activities such as portfolio reviews, intellectual property reviews, management operating mechanisms, and cross-functional initiatives.
Provide technical review for development and commercial agreements as well as support due diligence activities relating to acquisitions. Emphasize review of technical requirements/capability, financial risk, capital investment requirements, and protection of intellectual property.
Review all major capital appropriation requests for building modifications, major equipment purchases and installations for necessity, justification accuracy, impact on capital budget, as well as identifying potential alternative strategies to executive management. Participate in the design of new facilities and equipment.
Ensure compliance and audit/inspection readiness at all times.
Other duties as assigned
Emely Motol
Pharma -
NEWJob number: Job-00244070 Posted: 2023-05-24
製造(生産技術)
平均勤続年数20.8年／残業時間20～30時間7 - 10 million yen Other Pharmaceutical Research & Development
- Company overview
- Our client engages in research and development, manufacture, sale and import and export of pharmaceuticals.
- Responsibilities
- 同事業所はグループにおけるグローバル製剤の供給拠点であり、プロセス研究から工業化検討、治験薬・商業品の製造までを担っております。
今回は、商業生産や技術移譲に精通した生産技術者を募集します。
業務詳細：
治験用および商業用製剤業務
技術移譲時の生産プロセス立ち上げ・バリデーション
製造設備の日常的な維持管理・保全
Patrick Chang
Pharma -
NEWJob number: Job-00210485 Posted: 2023-05-24
[Osaka or Tokyo] Medical Writer of Drug Development
Great Company Culture8 - 14 million yen Other Pharmaceutical Research & Development
- Company overview
- In the global CRO market, it is a Japanese subsidiary of a top-level drug development contract entrusted organization.
- Responsibilities
- PREPARATION OF CLINICAL
TRIAL PROTOCOL- PREPARATION OF CLINICAL TRIAL SUMMARY REPORT
PREPARATION OF DRUG APPROVAL APPLICATION MATERIALS (CTD: COMMON TECHNICAL DOCUMENT) (CLINICAL PART ONLY)
PREPARATION OF INVESTIGATIONAL DRUG SUMMARY
REVIEW OF ABOVE-MENTIONED DOCUMENTS
CORRESPONDENCE BY AUTHORITIES (CLINICAL PART DOCUMENT CREATION, REVIEW, CONSULTING, ETC.)
GENERAL CONSULTING FOR DOCUMENT CREATION THAT MEETS REGULATORY REQUIREMENTS
CONTRIBUTING AS A LEADING ROLE IN THE ABOVE
APPROPRIATE GUIDANCE TO INEXPERIENCED MEMBERS AND CONTRIBUTION TO MEMBER GROWTH
Patrick Chang
Pharma -
NEWJob number: Job-00247941 Posted: 2023-05-24
高次細胞モデル構築技術を有する研究員
幹細胞やオルガノイドのハンドリングおよび分化制御技術の経験が活かせます。6 - 11 million yen Kanagawa Pharmaceutical Research & Development
- Company overview
- Our client is a biopharmaceutical company.
- Responsibilities
- 創薬研究および臨床開発のプロジェクトにおいて、以下の研究を推進する。iPSC、オルガノイドなどの高次細胞培養、分化技術の開発
ヒト組織・疾患を模したアッセイ系（in vitro 組織・疾患モデル）の開発
In vitro 組織・疾患モデルを起点とする創薬アイデアの創出とプロジェクトの企画立案
Patrick Chang
Pharma -
NEWJob number: Job-00248015 Posted: 2023-05-24
創薬化学研究者
リーダーとして研究チームを率いた経験ある方歓迎6 - 11 million yen Kanagawa Pharmaceutical Research & Development
- Company overview
- Our client is a biopharmaceutical company.
- Responsibilities
- 医薬品の研究、開発、製造、販売および輸出入を行う当社にて、創薬化学研究者としてご活躍いただきます。
■具体的な業務：有機合成研究・分子設計研究
薬理・製剤・ADMETデータ等の統合的な解釈を通じた創薬研究の推進
次世代創薬技術の開発研究
■職種の魅力：革新的な薬を自分自身の手で作り出すことを通じ、世界の医療に貢献できる。
Patrick Chang
Pharma -
NEWJob number: Job-00233809 Posted: 2023-05-22
Head of TA Cardiology, Pulmonology, Womens Health
Global pharma17.2 - 22.5 million yen Tokyo Pharmaceutical Research & Development
- Company overview
- Our client is one of the most well-established European-based international pharmaceutical companies in Japan.
- Responsibilities
- Managing and directing the Clinical Leaders and/or Medical Experts in given Therapeutic Areas.
Sets project-related objectives and personal development goals with Clinical Leaders and/or Medical Experts and conducts their annual performance evaluation.
Develop and maintain a motivated and competent staff by assuring that hiring, compensation, development, and advancement are all in line with talents and expectations and by working with key departmental managers across legal entities in planning, development and delivery of all services.
Responsible to ensure the development of a clinical strategy and the operational conduct of clinical development activities according to the approved clinical development plan for all clinical development projects within the Research and Development Organization that fall within the area of responsibility.
This includes development of new molecular entities from Phase II through Phase III and registration/launch, and development for marketed products designed to optimize product value e.g. Phase IV studies, development of new indications, or development of new formulations.
The purpose is to accelerate, streamline and strengthen the global clinical development effort so that investigational drugs may be approved more rapidly and positioned more competitively in the market place. For drugs already, marketed the purpose is to expand indications and/or support marketing on a global basis.
Close interaction with Global Therapeutic Area and respective Business Units to provide critical medical input.
Proactively manage the R&D portfolio of the respective Therapeutic Area, including proactive search, evaluation and execution of licensing opportunities in close interaction with the responsible functions, and appropriate decision making by the respective internal committees
Member of the global therapeutic area meeting, representing Clinical Development of the respective Therapeutic Area in Japan.
Develop and apply appropriate metrics to track and benchmark clinical development strategy activities and operational clinical development activities against internal and external best practices. The environment will be one of continuous improvement.
Emely Motol
Pharma -
NEWJob number: Job-00240774 Posted: 2023-05-22
プロジェクトマネジメント
医薬品の製剤・包装技術、注射剤技術において専門的知識を有している方必見です7 - 11 million yen Tokyo Pharmaceutical Research & Development
- Company overview
- Our client is a cutting-edge biotechnology company.
- Responsibilities
- CMC開発部門におけるバイオ医薬品の製造技術移転、製造所管理を中心としたプロジェクトチームのマネジメント（開発/上市プロジェクトのLCMを含むCMC製造管理戦略・計画策定とCMC関連部門の調整）
国内外の治験薬・商用生産体制の構築および治験薬・製品供給計画の策定と実行
CMC戦略、薬事規制等の情報収集及び発信
特に、製剤・包装製造所管理からスタート頂くことを想定
Patrick Chang
Pharma -
NEWJob number: Job-00248332 Posted: 2023-05-22
基盤技術研究
創薬化学、有機合成化学研究に関する知識・スキルをお持ちの方必見です5.18 - 9.5 million yen Other Pharmaceutical Research & Development
- Company overview
- Our client is a cutting-edge biotechnology company.
- Responsibilities
- 低分子医薬品探索における創薬化学研究のマネジメント及び推進
低分子医薬品探索における創薬化学研究および関連するインフォマティクス・AI・有機合成等の基盤技術研究のマネジメント及び推進
委託合成のマネジメント及び推進
Patrick Chang
Pharma -
Job number: Job-00248157 Posted: 2023-05-18
研究開発
グローバルに活躍5.93 - 9.68 million yen Other Pharmaceutical Research & Development
- Company overview
- Our client is in the pharmaceutical firm.
- Responsibilities
- 低中分子探索研究プロジェクトにおける化合物最適化研究のリーダー
プロジェクト内における合成担当者、共同研究等のマネジメント
新規テーマ、創薬基盤技術等の調査・提案
創薬プロジェクトに関わる社内外関係者との連携
Patrick Chang
Pharma -
Job number: Job-00248151 Posted: 2023-05-18
【横浜】創薬におけるバイオロジクスDMPK研究者
創薬の非臨床薬物動態研究での実務経験が活かせます。6 - 11 million yen Kanagawa Pharmaceutical Research & Development
- Company overview
- Our client is a biopharmaceutical company.
- Responsibilities
- 様々な新規分子形を有するバイオロジクスの薬物動態特性をメカニズムに基づき定量的に明らかにし、分子最適化の方向性を提示すると共にヒトPKPD予測を通してプロジェクトの成功確率を提示する。
技術課題解決のための新技術確立、ならびにアカデミアや海外関連会社との共同研究を通じた外部からの技術導入の推進役を担う。
Patrick Chang
Pharma -
Job number: Job-00245302 Posted: 2023-05-12
【滋賀】ブリスター包装の責任者／ドイツ本社メーカー
医薬品の製造およびGMPに関する知識 ある方お待ちしております。10 - 14 million yen Kansai Pharmaceutical Research & Development
- Company overview
- Our client is one of the most well-established European-based international pharmaceutical companies in Japan.
- Responsibilities
- メンバーをリードし、GMPとHSEに基づいた高品質な製品作りを保証する
GMPに基づき、最も効果的なプロセス（製造方法）を採用し、最も信頼できる高度な技術や情報を取得し、包装工程のバリデーションを実施する
発行された生産スケジュールに基づき、作業スケジュールや人員配置を管理し、効率的な生産体制を構築することにより、安定した供給と製品量を確保する
GMP/HSEの向上と製造コストの削減のため、生産方法の合理化、歩留まりの向上を図り、OE活動やデジタルトランスフォーメーションを推進する
GMP・HSEを遵守し、5Sを推進し、メンバー教育を通じて、作業者の安全・衛生に対する意識を高め、安全で清潔な作業環境を維持する
プロダクトサプライジャパンの方針に基づき、部下に教育の機会を与え、直接指導することで、一人ひとりの能力を培い、多様な業務に柔軟に対応できるようにする
労働者の健康状態／休日を把握し、生産スケジュールに基づいて残業／休日出勤／シフト勤務を管理することで、適切な労務管理を行う
チーム能力向上のため、責任をもってチームメンバーを育成する
将来のポートフォリオと数量予測を考慮し、短期・長期のチーム戦略および投資計画を構築する
Emely Motol
Pharma -
Job number: Job-00247785 Posted: 2023-05-12
医療AI
最先端技術で活躍10 - 15 million yen Tokyo Pharmaceutical Research & Development
- Company overview
- Our client assists international litigation and fraud investigations.
- Responsibilities
- 対話を通して顧客の抱える潜在的課題を抽出・具体化し、独自の自然言語処理AIエンジンをベースとした様々なテクノロジーによる解析結果に基づいたソリューションを提案します。
独自のAIを活用して様々な疾患領域の研究解析をリードし、ビジネスの基盤を築きます。
医学・薬学・生物学の広範な知識と同時に薬理学・医学における高度な専門知識と経験を駆使して業務遂行上の課題抽出や解決策を検討・探索すると同時に、広範な疾患領域の最新動向や最先端技術を把握し、実課題への還元を行います。
Patrick Chang
Pharma -
Job number: Job-00209439 Posted: 2023-05-04
【東京】創薬技術研究(遺伝子発現)
ウイルスを用いた遺伝子治療の研究の経験をお持ちの方必見です6 - 7.5 million yen Tokyo Pharmaceutical Research & Development
- Company overview
- Our client is a cutting-edge biotechnology company.
- Responsibilities
- 遺伝子治療用ウイルス、または腫瘍溶解性ウイルス等を用いた革新的な発現技術を研究開発する
新しい技術テーマを構想し立案する
技術を応用する疾患とコンセプト（パイプラインテーマ）を立案する
プロジェクトリーダーとして、社内外の専門家を巻き込みテーマを推進する
オープンイノベーションとして、競争力のある技術を評価導入する
Patrick Chang
Pharma -
Job number: Job-00242958 Posted: 2023-05-03
【茨城県】メディシナルケミスト
製薬企業勤務経験者必見です!8.1 - 11 million yen Other Pharmaceutical Research & Development
- Company overview
- Our client is a global pharmaceutical company with its own distribution channels around the world.
- Responsibilities
- タンパク質分解誘導剤のデザイン、および合成。またデザインに必要な薬理・ADME・物性データの理解、および構造活性相関の分析
開発候補化合物のCMC活動に向けたの予備的な合成法の検討
研究コンプライアンスを順守した実験業務の遂行
Patrick Chang
Pharma -
Job number: Job-00232031 Posted: 2023-05-03
プロセス開発研究 ケミカル医薬品
合成原薬プロセス開発業務経験をお持ちの方必見です6 - 11 million yen Tokyo Pharmaceutical Research & Development
- Company overview
- Our client is a biopharmaceutical company.
- Responsibilities
- ケミカル医薬品のプロセス開発研究の業務をお任せいたします。低中分子の新規合成医薬品原薬製造ルートの探索
プロセス開発、スケールアップ研究
国内外製造サイト技術部門への技術移管
治験承認申請における最新のグローバル規制要件を満たす品質管理戦略立案、データ取得・ドキュメント作成
新規な生産技術や製造設備に関する開発
Patrick Chang
Pharma -
Job number: Job-00207377 Posted: 2023-05-01
Application Scientist
Pricing and HEOR Hybrid position8 - 110 million yen Tokyo Pharmaceutical Research & Development
- Company overview
- Our client is a life sciences and materials science company.
- Responsibilities
- Provide scientific support to current and prospective customers, which includes demonstrating the optimal use of our life science software suites, facilitating interactions between customers and product development teams, and providing general scientific guidance
Engage in cutting edge scientific research and provide best practices for modeling automation to our customers
Consolidate the existing customer base
Publish scientific papers and present at conferences
Work from the Tokyo office when not traveling for company business
Martin Tsvetkov
Pharma