Jobs list of 6 - 14 million yen
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NEWJob number: JN -072024-137933 Posted: 2025-05-01
QA Manager
QA Manager10 - 12 million yen Tokyo Pharmaceutical Quality Assurance / Quality Control
- Company overview
- We are engaged in the research, development and provision of medical technologies in Japan. In particular, we focus on the development of innovative therapies and provide advanced technologies related to cancer treatment. We use a new therapeutic approach called photoimmunotherapy to target cancer cells for effective treatment. This technology combines light and drugs to selectively destroy cancer cells. In research and development, we are strengthening our collaboration with specialized institutions and universities in Japan and overseas to conduct clinical trials and commercialize the technology. We are committed to innovation in the medical field and to improving the quality of life of patients.
- Responsibilities
- Support Quality Assurance supervisor to achieve Japan Commercial Operations objectives from Medical device and drug perspective.
When Quality Assurance issue arises, lead to define the appropriate Quality measurement through the communication with the related internal, global and external parties.
Ensure full compliance with applicable regulations in Japan.
Oversee all activities or responsibilities that are delegated to external parties.
Martin Tsvetkov
Pharma -
NEWJob number: JN -072024-141505 Posted: 2025-05-01
Analyst
Analyst6 - 10 million yen Tokyo Pharmaceutical Market Access / Pricing / HEOR
- Company overview
- This is the exclusive business partner and adviser to biopharma senior management teams
- Responsibilities
- Demonstrated ability to be an important contact for the client in all communications
Ability to present independently to the client
Demonstrates strong understanding of assets that best fit the client
Ability to interact with partners and manage diligence requests
Able to trouble shoot assessment to evaluate target niches
Basic understanding of financial analysis and modelling, including DCF models and comparable transactions
Ability to author thought leadership pieces
Provide support in quality control and in ensuring the product is polished for Associate review
Having experience and understanding of the health care industry
Martin Tsvetkov
Pharma -
NEWJob number: JN -072024-143159 Posted: 2025-05-01
Medical Affairs PM
Medical PM8 - 14 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- We are a leading life sciences company based in the United States, with a parent company. Our core business revolves around the research, development, importation, manufacturing, and sale of pharmaceuticals and vaccines. Every day, we strive towards our mission and goals by protecting people\'s health and helping them build fulfilling lives. We aim to promptly address unmet medical needs in Japan and globally. Furthermore, we actively engage in activities to promote access to medicines, including product donations and supply to those in need through various programs and partnerships.
- Responsibilities
- 1) In research projects led by companies, manage research projects and contribute to the creation of evidence according to the plan.In the research project, as a member of the study team, in the process of planning, budget management, execution, and publication of results, internal related departments (R & D headquarters, legal / compliance department, purchasing department, finance department, etc.), the US headquarters, and outside the company Collaborate with partners.
In the research planning phase, develop a research timeline and budget plan, and lead the research feasibility assessment.
In the start preparation phase, we will be in charge of a wide range of tasks such as vendor selection, facility selection, various contract creation, and internal regulation assessment, and promote the project so that the research start can be achieved on timeline. In the execution phase, manage the project to proceed as planned through vendor management, cost management, and schedule management. We will also strive to ensure the quality of research.
Work to comply with compliance by conducting research based on ethical guidelines and various laws and regulations and guidelines while coordinating with related departments within the company.
For US headquarters-led research, work with headquarters personnel to promote the project.
2) In collaboration with researchers and their research institutes, the US headquarters, and related departments within the company (Medical Affairs, R & D Headquarters, Legal and Compliance Department, etc.), while maintaining the independence of researchers and the neutrality of research. Manage and execute researcher-led research (IIS) support operations and support the creation of innovative evidence by Japanese researchers.Responsible for researchers / research institutes and US headquarters in collaboration with related departments throughout the entire process of supporting IIS applications, contracting adopted projects, providing research funds and research drugs / compounds, preparing for research start, conducting research, and reporting results. Coordinate / negotiate with other parties and manage / execute IIS support operations.
In the field of cancer where research on new treatment methods is advancing, doctor-initiated clinical trials are also covered by the IIS support system, and if adopted by the examination, research funds and investigational drugs will be provided to provide future new cancer treatments. Support the development of law.
Collaborate / collaborate with related departments within the company to creatively find solutions when introducing an unprecedented new research support system.
Post the latest information on the IIS support system developed by the US headquarters worldwide on an external website, and provide detailed information on the system and procedures to researchers considering application in collaboration with related departments within the company. ..
When making a research contract with a research institution to which a researcher belongs, prepare a draft contract, negotiate a contract, and conclude a contract.
After starting the research, we will confirm the progress of the research (including the status of publication) based on the contract, arrange the provision of research drugs / compounds, and pay the research expenses according to the milestone.
Martin Tsvetkov
Pharma -
NEWJob number: JN -072024-143827 Posted: 2025-05-01
品質保証 QA
Global Company6 - 12 million yen Tokyo Pharmaceutical Quality Assurance / Quality Control
- Company overview
- We are engaged in the research, development, manufacturing, and sale of pharmaceuticals. We strive to maintain independent management, research, development, production, and sales functions, along with our unique international expansion efforts and the strengthening of our research and development capabilities. Focusing on strategic areas such as "cancer," we are accelerating the creation of promising new drugs, including antibody drugs. We also actively pursue global expansion, aiming to provide high-quality pharmaceuticals and services to patients worldwide.
- Responsibilities
- 医療機器、再生医療製品等を含む新たなモダリティへの業務展開
新たな技術の導入、技術の進化
サプライチェーンの多様化
グローバル製品（開発品・市販品）の増加
製造委託先、試験委託先ならびに原材料供給業者の増加
そのため、GQP/GMP/QMS/GCTP/GDP等に関する品質保証業務に精通した要員の補充が必要となった。
IND/IMPD、NDA/BLA作成及び推進、国内申請資料作成及び推進、その他CMC薬事にかかわる業務
Patrick Chang
Pharma -
NEWJob number: JN -072024-144988 Posted: 2025-05-01
【御殿場】バイオロジクス創薬推進における分析研究者
グローバルカンパニー！6 - 10 million yen Shizuoka Pharmaceutical Research & Development
- Company overview
- We are engaged in the research, development, manufacturing, and sale of pharmaceuticals. We strive to maintain independent management, research, development, production, and sales functions, along with our unique international expansion efforts and the strengthening of our research and development capabilities. Focusing on strategic areas such as "cancer," we are accelerating the creation of promising new drugs, including antibody drugs. We also actively pursue global expansion, aiming to provide high-quality pharmaceuticals and services to patients worldwide.
- Responsibilities
- 新規バイオロジクス開発や新規創薬技術開発におけるタンパク質分析ならびに新規分析技術の確立
Patrick Chang
Pharma -
NEWJob number: JN -072024-145099 Posted: 2025-05-01
[Tokyo/Shizuoka/Ibaraki] QA for Drug Development and New Product Launch
Rich Pipeline and Global Culture7 - 12 million yen Tokyo Pharmaceutical Quality Assurance / Quality Control
- Company overview
- We are a leading pharmaceutical company in Japan, offering a wide range of products in the medical field. Our product lineup includes various pharmaceuticals to support patient health, and we are also dedicated to research and development. We strive to develop new treatment methods and medications to contribute to the treatment and prevention of diseases. Additionally, we operate globally, providing our products to patients worldwide. We uphold high standards of quality and safety, contributing to the advancement of healthcare and the well-being of patients.
- Responsibilities
- Contribute to development projects by ensuring the quality of investigational drugs used in clinical trials conducted globally and complying with regulations such as GMP.
Promotion of quality assurance operations such as management of investigational drugs, investigational drug substances and new product manufacturing contractors, change management in the development phase, implementation of quality audits, shipment of investigational drugs by appropriate product quality management, etc.
Building and collaborating with joint development partners
Improvement of global quality assurance system for developed products, continuous improvement, promotion of new regulation compliance
Promote regulatory inspection response and inspection preparation in cooperation with related departments such as laboratories, manufacturing contractors, and supply chains so that early application and launch of new products can meet and respond to regulatory requirements globally.
Participate in the global working team within Quality Assurance and Quality Technology to solve quality assurance issues and improve and improve the quality assurance system.
Initial development phase Quality assurance work at product manufacturing plants such as regenerative medicine
Martin Tsvetkov
Pharma -
NEWJob number: JN -072024-167442 Posted: 2025-05-01
Partner Specialist (SDR)
Global working environment/Cloud technology6 - 8 million yen Tokyo Information Technology IT Sales / Business Development
- Company overview
- We are a global IT services and consulting company that supports business transformation through digital, technology, and consulting services. We provide digital strategy, IT consulting, systems integration, and outsourcing services, aiming to drive industry innovation and efficiency. Additionally, we leverage our global network and advanced technologies to deliver optimal solutions to our clients.
- Responsibilities
- The Partner Advisor is a dedicated point of contact for cloud partners, guiding them through all stages of business development to build and grow their cloud business and provide the best experiences for end customers. The core responsibilities include:Sales and Upselling:Conduct inbound and outbound product/service sales and upselling.
Execute daily outbound phone calls/emails, contact decision makers, build quick rapport, and assess needs.
Explain technical products/solutions and value propositions to businesses across various verticals and sizes, detailing how they address client needs.
Execute outbound prospecting campaigns to source, contact, and engage prospective customers interested in evaluating products.
Develop and lead outbound campaigns from idea generation through to initial pitch and pipeline qualification.
Lead and contribute to team projects to develop and refine the sales process.
Develop and codify best practices and sales workflows for interactions with prospects.
Achieve or exceed monthly sales quotas.
Reach out to existing customers to pitch new ancillary products or increase spending on currently used products.
Troubleshoot small technical setup issues or route them to relevant teams.
Renewals (Cloud):Manage the customer renewal sales process, identifying up-sell and cross-sell opportunities within accounts, and closing these agreements before contract expiration.
Educate customers on digital products.
Participate in the design, development, and implementation of programs to increase cloud renewals business.
Analyze data trends, market dynamics, and customer performance, identify opportunities, and create implementation plans to maximize results.
Support regional leads and partner community with training, materials, and ongoing support.
Engage and coordinate internal groups as needed to resolve customer issues and maximize customer retention.
Increase the number of upgrade executions.
React to client business needs and adapt internal procedures to provide services.
Manage daily renewal opportunities in the CRM system.
Work with account managers to provide clarity around executing upgrades.
Dejiddolgor Suuri
Tech Services -
NEWJob number: JN -072024-4437 Posted: 2025-05-01
Japan Risk Management Leader
Rich pipeline, both Clinical and PMS9 - 14 million yen Tokyo Pharmaceutical Pharmacovigilance
- Company overview
- Our client is a leading global pharmaceutical firm with a presence in about 150 countries and a workforce of around 40,000 employees. The company is dedicated to advancing healthcare through innovative treatments across various therapeutic areas.
In Japan, the firm employs over 2,500 professionals focused on delivering solutions tailored to the specific needs of the local population. By integrating global advancements with local insights, the company collaborates closely with healthcare providers to ensure effective and accessible therapies.
Committed to sustainability and corporate responsibility, the firm strives to improve patient outcomes and enhance the quality of life. Its efforts make significant contributions to both the local and global healthcare landscape. - Responsibilities
- ake full accountability to create, implement and verify J-RMP activities including EPPV, risk communication activities and aggregate reporting such as J-DSUR, J-PSUR, Periodic Infection Report and Non-serious unlisted periodic report including reports for medical devices and all activities related to Post-Marketing Surveillance/Clinical study/Database research.
Take full accountability to prepare Re-examination dossier and GPSP compliance inspection in responsible products/compounds.
Lead and manage PvA and PMSO in responsible products/compounds.
Lead and facilitate J-SMT meeting in collaboration with JPKK’s key stakeholders including JCoT members.
As an extended member of Global Safety Management Team(G-SMT), liaise with G-SMT of responsible products/compounds.Join JCoT, NPI and other related committee with license partner companies as a representative for J-SMT of responsible products/compounds and proactively lead safety risk management related discussions and take necessary actions by covering early stage of clinical development though postmarketed phase of products.
Lead and contribute to the prevention and rapid resolution of local safety risk management related issues including timely stake holder management (internal and external) of responsible products/compounds.
Plan and monitor budgets and controls expenditures for responsible products/compounds in collaboration with Group manager/ Director.
Contribute to the implementation of continuous process improvements from advanced safety management point of view by utilizing latest technologyes while enhance sustainable efficiency in collaboration wih SPMD.
Understand the rule and principle of the relevant regulations such as PMD Act., GCP, GVP and GPSP and ensure compliance to those regulations, within own responsibility.
Patrick Chang
Pharma -
NEWJob number: JN -072024-9212 Posted: 2025-05-01
【茨城・筑波】薬理受託試験サービスマネージャー（オンコロジー領域）
ピープルマネジメント経験が生かせます8 - 11 million yen Ibaraki Pharmaceutical Research & Development
- Company overview
- We produce a variety of mice and rats, and also provide feed and bedding. This allows researchers to focus on animal care, management, and research. Additionally, we collaborate with the United States to conduct virus testing on animal cells and provide contract manufacturing of monoclonal antibodies. Our fundamental principle is to produce and supply experimental animals based on scientific knowledge, supporting the development of life sciences by ensuring a stable supply of high-quality experimental animals that become the global standard.
- Responsibilities
- ・Oncology領域受託試験サービスの業務管理・予算達成
・PDX（Patient-Derived Xenograft）/ Immuno-Oncology事業の拡大戦略策定 / 実行
・受託試験サービスにおける顧客対応
・従業員管理
Patrick Chang
Pharma -
NEWJob number: JN -072024-33198 Posted: 2025-05-01
サービス推進（企画／運営）
ネットワークもしくはセキュリティ分野に関する知識、経験をお持ちの方必見です。6 - 9.3 million yen Tokyo Information Technology Helpdesk / Support Engineer
- Company overview
- Our client is an information and telecommunications manufacturer.
- Responsibilities
- 同社取り扱いの海外のネットワーク・セキュリティ製品のサポートサービス全体の企画・運営に携わっていただきます。
製品ごとにチームが分かれているため、入社後はいずれかの製品を担当するチームに配属となります。 テクニカルサポート (お客様対応、トラブルシューティング、調査／解析、メーカエスカレーション等）
サービス開始前の新商材の評価・検証
サポートサービスの企画、構築及び運営
Jinxiu Han
Tech Services -
NEWJob number: JN -072024-35827 Posted: 2025-05-01
HR
ベンチャー企業でのHR6 - 8 million yen Tokyo Human Resources HR Generalist
- Company overview
- We provide a platform that enables the rapid construction of business systems, empowering many individuals to become product creators. This platform offers highly flexible and scalable core systems for large and medium-sized enterprises.
In recent years, as the trend of combining cloud SaaS specialized for specific use cases accelerates, we are pioneering the construction of next-generation business application platforms. In the Japanese market, where outsourcing to system development companies is common, we provide backend and frontend application development and business consulting on our own platform.
By leveraging the latest technology and creativity, we aim to support the future society by solving corporate management challenges. - Responsibilities
- 採用・評価制度・人材開発を中心に組織を一緒に創ってくださる方を募集します。事業を成長に導くための「人」と「組織」にまつわる戦略策定と実行を実現していただきます。 業務内容：
事業計画の実現のための組織設計
採用戦略の立案と実行
評価制度の設計、継続的なアップデート
オンボーディング、人材開発の企画立案・実施
Misato Nakao
Corporate Services -
NEWJob number: JN -072024-142337 Posted: 2025-05-01
メディカルアフェアーズ本部 肺高血圧症疾患領域スペシャリスト
メディカルアフェアーズ本部 肺高血圧症疾患領域スペシャリスト6 - 10 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- Our client is a leading global pharmaceutical firm with a presence in about 150 countries and a workforce of around 40,000 employees. The company is dedicated to advancing healthcare through innovative treatments across various therapeutic areas.
In Japan, the firm employs over 2,500 professionals focused on delivering solutions tailored to the specific needs of the local population. By integrating global advancements with local insights, the company collaborates closely with healthcare providers to ensure effective and accessible therapies.
Committed to sustainability and corporate responsibility, the firm strives to improve patient outcomes and enhance the quality of life. Its efforts make significant contributions to both the local and global healthcare landscape. - Responsibilities
- Responsible to develop the Medical Affairs product strategy through the analysis of medical needs collected from all internal & external stakeholders of the therapeutic area
Responsible for managing MAF study / publication portfolio in alignment with brand strategy
Responsible for people and operational budget management of PH (Pulmonary Hypertension) therapeutic area
Day to day project management for activities based on the Medical Affairs Plan in responsible disease areas
Responsible for ensuring that all Medical Affairs activities are compliant with Japan Legislation and HCC (Healthcare Compliance) rules.
Patrick Chang
Pharma -
NEWJob number: JN -072024-142574 Posted: 2025-05-01
Regulatory Strategist
RA8 - 12 million yen Tokyo Pharmaceutical Regulatory Affairs
- Company overview
- Our client is one of the most well-established European-based international pharmaceutical companies in Japan.
- Responsibilities
- Build a registration strategy for efficient product development in Japan to get fast approval of new projects (new product, new indication, new dose & administration, new formulation, etc.).
Coordinate the relevant functions to prepare the documents which should be submitted to PMDA and/or MHLW such as the documents relevant to PMDA consultation and Orphan Drug Designation.
Support the dossier manager to lead the relevant functions to prepare the required documents for NDA/sNDA submission and answer documents to inquiries during NDA/sNDA review by PMDA, and conduct the following activities.
Ensure other functions to prepare the documents to be submitted to Health Authority on products.
Contribute to the global regulatory activities on projects in charge by inputting regulatory strategy in the global regulatory strategy.
Provide Global Regulatory Team (GRT) with the Japanese legal/regulatory requirements and Japanese development strategies if necessary.Graps the regulatory information such as HA’s movement, legal requirement on NDA/sNDA guidelines, etc
Martin Tsvetkov
Pharma -
NEWJob number: JN -072024-148333 Posted: 2025-05-01
ファーマコビジランス職
語学力を活かしてグローバルに活躍6 - 12 million yen Tokyo Pharmaceutical Pharmacovigilance
- Company overview
- Our client a major Japanese pharmaceutical company engaged in the research, development, manufacturing, and sales of pharmaceuticals. Our group promotes four business areas—new drugs, generics, vaccines, and OTC products—to meet diverse medical needs. By expanding our operations globally, we aim to provide innovative treatments to a wide range of patients. Additionally, we possess advanced technological capabilities and well-equipped facilities to support our research and development. We actively conduct clinical trials both domestically and internationally, striving to demonstrate leadership in the pharmaceutical industry while emphasizing our commitment to contributing to society as a whole.
- Responsibilities
- グローバルPV企画・管理業務
海外子会社（特にアジア地域）のPV業務の管理
オーバーサイト
海外子会社PV担当者と連携し、グローバル基準に準拠したローカルでのPV systemの維持・管理
海外子会社のPV組織立ち上げ
ガバナンス管理
Patrick Chang
Pharma -
NEWJob number: JN -072024-5291 Posted: 2025-05-01
【東京】プロジェクトマネージャー
製薬企業またはCROでグローバル試験のPM経験3年以上お持ちの方必見です。7 - 9.5 million yen Tokyo Pharmaceutical Clinical Development
- Company overview
- Our client is a Contract Research Organization (CRO).
- Responsibilities
- 当社が実施するプロジェクトの進捗管理と適切な予算管理をお任せします。
担当プロジェクトの課題や変更管理など、クライアントとの窓口責任者として様々な課題の解決に向けて社内外の調整をお任せします。
国内とグローバル両方の標準手順を理解し、医薬品・医療機器等の試験チームのPM経験を積んでいただくことを期待しています。
また顧客満足度の向上にむけて、さまざまは提案をしていただいたり、サービスプロバイダーとしてプロジェクトマネジメントの専門ノウハウを蓄積していくことも期待しています。
Patrick Chang
Pharma -
NEWJob number: JN -072024-30044 Posted: 2025-05-01
Product Marketing (TAVI) | プロダクトマーケティング（TAVI）
製薬業界マーケティングからのご応募も可能です！7 - 9 million yen Tokyo Medical Device Marketing
- Company overview
- Our primary business is the import and sale of medical devices, offering devices for testing and treatment of cardiovascular diseases. We have also entered the field of neurosurgery, which is a new business area for us. Our mission is to help healthcare professionals treating patients with cardiac, neurological, and chronic pain around the world gain access to superior treatment tools. We focuse on the development of medical technologies and services that contribute to the reduction of risk and the successful treatment of all patients.
- Responsibilities
- The TAVI Product Manager is responsible for setting strategic direction in Japan for the portfolio and for tactical implementation of activities aligned to a patient-centric, customer-centric and goal-achieving culture, leading to optimal clinical adoption, outcomes, and customer satisfaction within the space.The TAVI Product Manager is responsible for the following related to their portfolio:
Main responsibilities:
Develop Japan-specific marketing strategies and tactics for new product launches including market analysis, clinical strategy, reimbursement strategy, product positioning and messaging.
Contribute to the achievement of objectives via development and close execution of annual marketing plans.
Design and prepare the workflow, procedure, logistics and documentation required for product launch and business operation driving the cross-functional teams.
Plan and execute TAVI marketing tactics, especially for messaging for brand positioning and differentiation, peer to peer event to demonstrate product benefit, and activities to deepen customer engagement in TAVI market.
Set appropriate KPIs (leading KPIs, activity KPIs, clinical KPIs and performance KPIs) for marketing tactics, analyze data and track to take timely corrective actions as necessary
Leverage customer relationships, technical expertise and product knowledge to plan and coordinate new launches, and provide the sales team with appropriate messaging, campaigns and tools highlighting objective, relevant differentiation.
Develop promotional tools and optimize others provided by Global Marketing; launch with appropriate localization, training, and tracking.
Create open, productive lines of communication between the sales and clinical team and all other areas that affect the product: Regional and Global Marketing, RA, QA, etc.
Provide clinical and sales staff with clinical knowledge and promotional guidance, ensuring products are targeted appropriately to satisfy customer needs and expectations.
Stay up-to-date on key publications, trials, indications, society guidelines, and market dynamics and reflect to the communication / marketing strategy
Interface with Public Relations firms, market research companies; design agencies and other vendors and customers to effectively grow business in a profitable manner while maintaining a customer focus throughout all activities.
Develop and maintain professional relationships with key customer accounts as well as market influencers.
The TAVI Product Manager is responsible for achievement of the goals and objectives associated with their products including revenue, margin, and expense budget. Business Process goals will be measured against commitments in the annual marketing plan. Strict compliance with the company's Quality System and all Ethics/Compliance guidelines is required
Shotaro Tsubaki
Medical Device -
NEWJob number: JN -072024-142387 Posted: 2025-05-01
[Daiichi Sankyo] プロジェクトマネジメント
CROで開発業務5年以上かつプロジェクトマネジメント業務の経験をお持ちの方必見で7 - 10 million yen Tokyo Pharmaceutical Clinical Development
- Company overview
- Our client a major Japanese pharmaceutical company engaged in the research, development, manufacturing, and sales of pharmaceuticals. Our group promotes four business areas—new drugs, generics, vaccines, and OTC products—to meet diverse medical needs. By expanding our operations globally, we aim to provide innovative treatments to a wide range of patients. Additionally, we possess advanced technological capabilities and well-equipped facilities to support our research and development. We actively conduct clinical trials both domestically and internationally, striving to demonstrate leadership in the pharmaceutical industry while emphasizing our commitment to contributing to society as a whole.
- Responsibilities
- 開発プロジェクトにおけるプロジェクトマネジメントとして、グローバルプロジェクトチームのマネジメント、開発戦略計画、予算、タイムラインおよび課題管理・解決をお任せいたします。
Patrick Chang
Pharma -
NEWJob number: JN -072024-146307 Posted: 2025-05-01
【東京】臨床開発プロジェクトマネージャー
臨床開発プロジェクトマネージャー経験者必見です!6 - 9 million yen Tokyo Pharmaceutical Clinical Development
- Company overview
- We are committed to providing high-quality products and delivering appropriate safety information to patients and consumers worldwide. In our pharmaceutical business, we focus on developing anticancer drugs and other medications, offering treatments for cancer, immunology, allergies, and urology. Additionally, in our consumer healthcare business, we cultivate well-loved brands that contribute to the health and well-being of consumers over the long term.
- Responsibilities
- 臨床開発プロジェクトのスケジュール・リソース・コスト管理
社内意思決定プロセス管理
関連部門（臨床開発、薬事、非臨床、CMC等）で構成されるプロジェクトチームのコミュニケーションマネジメント
共同開発先・導出入先との協業プロジェクトのアライアンス業務
歓迎条件:
海外スタッフを含むグローバルチームでの業務経験
上級レベルの英語コミュニケーション能力 （グローバルチーム会議をファシリテートできる会話能力）※海外拠点や海外他社協業先とのグローバルプロジェクトの担当機会あり
抗がん剤領域の新薬開発経験
プロジェクトマネジメント管理ソフトの使用経験（例：MS-Project、Planisware等）
Project Management Professional （PMP）資格
Patrick Chang
Pharma -
NEWJob number: JN -072024-151560 Posted: 2025-05-01
Game Director | ゲームディレクター
新規IPの立ち上げチャンス・ビジョンがある方歓迎6 - 9 million yen Tokyo Information Technology Web Design / Producer
- Company overview
- IT solution company involved in a diverse range of development fields, including games, smartphone applications, web systems, VR content, and AI systems.
- Responsibilities
- ゲーム開発の企画立ち上げ、開発、運用などのディレクションをお任せ致します。ゲームプロジェクトの責任者としてタイトルの開発からリリース、運用をリードしていただきます。
業務内容：
企画書・仕様書の作成
工数見積もり
プロジェクト全体のディレクション
クオリティ管理・スケジュール管理
クライアントとの折衝
Kento Hartman
IT Online -
NEWJob number: JN -052025-187630 Posted: 2025-05-01
人事
メーカーでの人事業務経験が活かせます。6.6 - 9.65 million yen Gunma Human Resources HR Generalist
- Company overview
- Our client is a well-established Japanese chemical company with a rich history. It has achieved global expansion and currently operates across three key pillars: material technology, application technology, and simulation technology. Their primary product portfolio include semiconductor and electronic materials, automotive parts and lithium-ion battery materials, functional materials, and chemical products. Their commitment to sustainability drives their efforts to contribute to a more eco-friendly society.
- Responsibilities
- 新卒、中途採用
社員教育
アセスメント（社内昇格試験）
労働時間管理
社会保険
健康管理（含休・復職フォロー）
評価制度（MBO）運営、管理
人事システムの管理・操作（Company、Success Factors）
派遣社員管理
Cindy Wong
Corporate Services