Jobs list of 6 - 16 million yen
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Job number: JN -012025-183480 Posted: 2025-05-02
Sr. Manager - Tax
Leading provider of mobile compensation services10 - 12 million yen Tokyo Accounting & Finance Tax / Treasury
- Company overview
- We are a provider of mobile phone insurance services, headquartered in the United States and operating globally as part of a larger group. We offer insurance services for mobile devices and have established a significant presence in the Japanese market. To ensure users are not inconvenienced in case of trouble, carriers provide compensation services such as delivering an equivalent device to the user\'s specified location within two days. We work closely with our group companies to provide insurance services to major telecommunications carriers in Japan, supporting the peace of mind in digital life for numerous consumers.
- Responsibilities
- Leading provider of cell phone compensation services seek an experienced Finance Sr. Manager who leads corporate tax and treasury procedures to ensure compliance with corporate policies as well as other underlying local tax and bank regulations. This person will manage overall tax matters including periodical tax remittance, provisional tax estimations, annual various tax filings as well as other regional treasury matters for all group entities as part of centralized shared services.
The Finance Sr. Manager will report to the Sr. Director of Accounting Reporting & Taxation and work closely with the others in the organization. The successful candidate possesses leadership capabilities, solid operational and technical tax filing and compliance background, and works proactively to drive results. This person is a self-starter, flexible, having ability to deal with ambiguity with high communication skills, and can enjoy bearing responsibility to provide proposals on a wide range of tax issues.The successful candidate possesses leadership capabilities, solid operational and technical tax and accounting background and works proactively to drive results. This person is a self-starter, flexible, having ability to deal with ambiguity with high communication skill, and can enjoy bearing responsibility to provide proposals for important business decision.This position is a potential Director of Finance position for the successful candidate when you pursue higher level of management role in Finance.
You will enjoy diversified, multi-national and cultural work environment.
You can gain various opportunities based on your experience and skill set in the Japan Regional Finance Organization to develop your career.
Hybrid working style will make your work and life balanced.
職務内容
Responsible for effective planning, execution, and completion of corporate, local, consumption, property and withholding tax returns for all regional entities
Co-work with corporate tax team and provide local tax information for global consolidated tax filing purposes
Proactively interact with various individuals in the organization to gather information, resolve tax-related problems and make recommendations for business and process improvements.
Continuously updating own knowledge about Japanese tax with the resources of third-party tax consulting
Prepare quarterly corporate tax projections, make periodical tax remittance, and monitor tax transactions throughout the year
Perform periodical revenue stamp and consumption tax reasonability test to comply with local tax regulations
Prepare annual cash flow projections and monitor cash positions for periodical updates
Keep relations with local banks and corporate treasury to seek out the option of funding, and issue Japan bank reporting as necessary basis
Assist any other tax and treasury related ad hoc matters
#poweredjob1
Maria Nakata
Corporate Services -
Job number: JN -102024-178664 Posted: 2025-05-02
【東京】翻訳担当(製品に関わる技術文書)
翻訳（英訳）の実務経験者必見です!8 - 12 million yen Tokyo Industrial Technical Advisor
- Company overview
- We are a company that develops and manufactures semiconductor manufacturing equipment and related precision processing technologies using advanced technologies. As a leading company in microfabrication technology, the company is highly regarded in a wide range of industrial fields, particularly in the semiconductor industry. Its products and technologies are indispensable in the manufacturing process of semiconductor devices, enabling high-precision processing and quality control. DISCO also has a global presence, providing innovative solutions to customers in Japan and overseas. We are committed to sustainable growth and social responsibility, and contribute to future industrial development through technological innovation.
- Responsibilities
- 【メイン業務】取扱説明書、仕様書、作業要領書、調査レポート、システムUI等の英訳
翻訳文書の校正
翻訳スケジュールの調整・管理、サプライヤ対応
【業務改善活動(PIM)に関わる業務全般】改善案アイデア出し・推進・実施/毎月開催される他部署対戦で使用する資料の作成・発表
【目標管理活動(MBO)に関わる業務全般】(目標管理活動とは…企業活動の質ををめていくために、いくつかのの標を設定し全社で1年をかけて取り組む活動。全社と部部毎のテーマをそれぞれ設け、定期的に達成度合いを測定)担当テーマについて達成状況の進捗確認
他メンバーの取り組み意識を向上させる施策の企画推進
Misato Aiba
Electronics -
Job number: JN -072024-14203 Posted: 2025-05-02
【東京】MSL（未経験）
豊富なキャリアパス／研修・教育環境充実6.5 - 9.5 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- We are a global healthcare company and the largest provider of biopharmaceutical development and commercial outsourcing services. In today\'s rapidly changing environment surrounding the healthcare industry, we are making a significant contribution to the development of the industry through its four business segments: Clinical Development, Sales & Marketing, Investment & Alliances, and Consulting. The company, which has supported the development and commercialization of the top-selling drugs worldwide, plans to substantially increase the number of CRAs as it continues to increase projects in large-scale global studies, the anticancer field, the central nervous system field, and other rheumatology fields.
- Responsibilities
- 国内トップクラスの規模とプロジェクト受託実績を誇る同社の一員となり、MSL（メデカル・サイエンス・リエゾン）としてクライアントビジネスおよび患者さんにとっての最適な治療法の確立に貢献していただきます。
MSLは、 担当する疾患領域における最新の科学知識に基づき、社外医科学専門家と同じ科学者同士の立場で医学的・科学的情報の交換並びに意見交換を通じて、アンメット・メディカル・ニーズ（注：未だ満たされていない医療ニーズ、有効な治療方法がない疾患に対する医療ニーズ）を収集し、育薬に貢献することが主な役割です。
具体的には、担当製品に関連する疾患・治療の国内外の最新情報を収集し、データの解釈や今後必要なデータ等について医療者と議論を行い、インサイト（知見）を得て、より安全な薬剤の使い方の検討や、より使いやすい薬剤への改善に活かします。
これにより、治療の効率が上がったり、適応症（対象となる疾病）が増えたり、次の新薬開発のヒントを得ることで、薬剤価値の最大化を実現させることが主な業務です。
そのほか、医療者からのリクエストに基づいた質疑対応や、臨床研究の相談窓口としての役割もあります。
Patrick Chang
Pharma -
Job number: JN -052025-187623 Posted: 2025-05-02
【PM】大手SIerのグローバルネットワーク構築PRJの推進
PMとしてプロジェクト推進を行ったご経験者必見です!8 - 9 million yen Tokyo Information Technology IT Management
- Company overview
- -
- Responsibilities
- グローバル案件のため、海外のお客様との折衝や会議運営、PRJ資料作成などが発生します。
現在は事業部長が単独で参画していますが、入社後は事業部長と2人体制で参画いただき、約3か月間のフォロー期間を経て、独り立ちいただく予定です。
Iori Ohara
Tech Services -
Job number: JN -072024-141139 Posted: 2025-05-02
[Ascent] CMC RA
CMC RA8 - 12 million yen Tokyo Pharmaceutical Regulatory Affairs
- Company overview
- Newly started domestic CRO, rapidly expanding in APAC and focusing on smaller to mid sized pharmaceutical companies looking to enter Japan/APAC
- Responsibilities
- Prepare documentation (including for Cartagena Type 1 Applications and CMC Consultations) with team under direction of scientific/ management lead
Interact and manage project communications with clients in bilingual environment
Support interaction with regulatory authorities
Patrick Chang
Pharma -
Job number: JN -072024-143552 Posted: 2025-05-02
R&D Japan/ Group Manager, Innovation Management Office
Alliance / Open Innovation8 - 16 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
- All R&D communication physically such as THM and/or virtually such as via e-mail/R&D Portal site etc. R&D regular leadership communication such as RD SLT and LT.
Any R&D responsible technology-based innovation initiatives such as Robotic Process Automation, Cloud based cross functional team communication, as well as center of excellence to shard service provider at R&D. In addition to that the Group will provide service to lead non-R&D specific career development program to whole R&D, as well as to be responsible for new grads program execution.
Patrick Chang
Pharma -
Job number: JN -072024-145164 Posted: 2025-05-02
Medical Information Specialist/Mangger
医療業界における顧客対応経験が活かせます。6 - 12 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- This company is the world\'s leading pharmaceutical company.
- Responsibilities
- （1）担当する領域の製品、開発品に関する学術的な問い合わせ（電話およびMR経由の依頼）の二次対応（製品情報センターで回答できなかった場合の対応）…文献調査、文献選定、文献内容の要約もしくは関連部署からの情報収集により回答を準備し、電話または文書にて実施（2）問い合わせ対応データから顧客のニーズを判断し、提供用のQ＆A、製品情報センターの口頭回答用のQ&Aを作成、改訂（3）担当する領域の製品に関する顧客からの要望・提案、問い合わせにより生ずるリスクに対し、リスク最小化およびビジネス最大化のための対策を講じる（4）担当製品の関連情報の提供・収集を行い、医療現場における適正使用を確保（5）販売提携などのコ・プロモーション製品においては、提携会社と円滑に情報共有が実施できる体制を構築し、両社における情報提供の整合性を確保（6）グローバルMI担当領域製品チームの一員として下記業務を実施英語での科学的な回答文書（GSRD）の作成、レビューおよびGSRDの日本向けのローカライズを実施
海外からの英語での問い合わせに対応(文書回答)する。
（7）GPT（グローバル製品チーム）に参加し、日本のマーケット状況等を共有し、グローバルとしての最適なアクション立案に貢献※専門管理職は上記に加え、マネジメント業務について相応の役割を担っていただきます。
Martin Tsvetkov
Pharma -
Job number: JN -072024-145172 Posted: 2025-05-02
Medical Affairs Review Specialist
Medical review7 - 10 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
- 資材・スライド等の検証
社内コンプライアンス研修
部門横断プロジェクトのリード
Martin Tsvetkov
Pharma -
Job number: JN -072024-38165 Posted: 2025-05-02
Medical Science Liaison (MSL) - 自己免疫領域
MSL position at global maker with strong pipeline7 - 11 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- We are a global pharmaceutical and clinical research company based in the United States. Through pharmaceuticals, we help people live healthier, healthier, and longer lives. Through productive agreements and partnerships around the world, we have grown to become one of the world\'s leading pharmaceutical companies by expanding its scale and developing pharmaceuticals at low cost. We have many employees who are committed with sincerity in a culture of excellence and are committed to further expansion.
- Responsibilities
- 業務内容：
領域専門医等のリクエストに応じて、最新医学・科学情報を提供・議論する。
領域専門医等の意見、疑問、ニーズならびに共同研究などの機会を探索・収集し、社内関連部署と連携して解決策を探る。
サイエンティフックエキスパート(SE)との関係構築および維持をする。
メディカル部門主導イベント（アドバイザリーボード等）を社内医学専門家と協働して実施する。
Yui Osone
Pharma -
Job number: JN -072024-30356 Posted: 2025-05-02
【東京】開発薬事※マネージャー候補
薬事部門のマネジメント経験者必見です!7 - 12 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- Our client is providing drug development service.
- Responsibilities
- 部門の管理、人財マネジメント
営業活動
部門の予算管理
医薬品・医療機器関連の治験相談
メディカルライティング業務管理
医薬品・医療機器に関する法規制への対応業務
各国申請代理人との連絡・調整
当該国薬事規制等の調査
アジア地域における医薬品・医療機器開発戦略コンサルティング （各種試験成績・資料の評価、医薬品・医療機器承認申請に係る当局対応、申請届出等）
Patrick Chang
Pharma -
Job number: JN -072024-138844 Posted: 2025-05-01
Senior Specialist Quality Assurance / PV Audit
Global Company8 - 10 million yen Tokyo Pharmaceutical Pharmacovigilance
- 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
- Prepares, conducts QA audits, generates audit reports, communicates results to the relevant QA management and relevant business stakeholders (e.g. Clinical trial team), and interacts with various teams to ensure corrective and preventative actions are taken to bring QA observations to closure as applicable.
Activities may include GCP and/or PV related routine and directed audits of investigator sites, country offices, vendors, regulatory documents and marketing applications, third party/business partner collaborations and due diligence activities.
Participates in the development/enhancement of QA procedures, guidance documents and audit tools to ensure QA consistency globally.
Promotes standardization of auditing approach within QA.
May represent QA as a single point of contact and provide QA guidance for studies in a certain Therapeutic Area (TA) or in certain countries to achieve continuous quality improvement and effective quality assurance.
Interfaces with relevant stakeholders, including regulatory, clinical and development sub-teams, as appropriate to provide Good Clinical Practice/Pharmacovigilance QA expertise.
Contributes to the QA strategy and supports QA goals for the aligned studies/countries in the Region.
Proactively identifies analyses and leverages quality indicators and data to identify potential trends and risks to address and complete risk-based QA assessments and to support the implementation of associated risk mitigation strategies.
In alignment with risk assessments, supports the identification of audit substrate for scheduling, as appropriate.
In collaboration with the QAL, actively contributes to the quality management oversight, in the development of clinical risk assessments and quality oversight initiatives (quality plan, quality agreements) as needed.
Support Significant Quality Issues management for assigned studies, including assessment of potential root causes and remediation (corrective and preventative actions) as needed.
Ensures appropriate and timely escalation of quality issues, including potential misconduct or issues of significant deviation with projects/products, to the QAL, TA Head and line manager.
Provides inspection management support as appropriate.
Develops and delivers awareness sessions with minimal supervision on various GCP and/or PV topics internally and externally.
Acts as a strong technical resource and is called upon to resolve GCP/PV issues based on knowledge of relevant SOPs (Standard Operating Procedures), GCP, PV regulations and guidelines as well as local regulations.
Martin Tsvetkov
Pharma -
Job number: JN -122024-181677 Posted: 2025-05-01
【東京】ファーマコビジランス職（グローバルPVアフィリエート管理）※豊富なパイプライン有する製薬企業
海外駐在員としての選出も視野に入れた育成あります6 - 11 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
- ■業務内容：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
■キャリアパス：当人の適性を踏まえ、OJTやジョブローテーション等を活用してキャリアを形成し、幹部職やマネジメント職の登用を視野に入れた育成
当人の適性を踏まえ、海外駐在員としての選出も視野に入れた育成
Martin Tsvetkov
Pharma -
Job number: JN -072024-35074 Posted: 2025-05-01
Circuit Design | 回路設計エンジニア
Circuit Design of wireless chargers8 - 12 million yen Tokyo Industrial Electrical Engineer
- Company overview
- We are a startup originating from an American university, aiming to achieve a "wireless digital world" through wireless power transfer technology. We engage in the development, manufacturing, sales, and import/export of semiconductors, robots, medical devices, and other products. We also operate businesses such as Factory Automation, Building Management, and Medical Implants, contributing to the innovation of customers aspiring for "digitalization" through IoT
- Responsibilities
- 当社が提供する空間伝送型ワイヤレス給電ソリューションの送電機、受電機製品の回路設計に関する業務を行って頂きます。
業務内容：
電気及び回路設計
設計業務に関わるマネジメント業務（関係会社との折衝、日程管理、コスト管理、量産導入、品質管理、現場立ち合いなど)
設計業務に関わる評価および解析
Kosuke Kanazawa
Electronics -
Job number: JN -072024-9016 Posted: 2025-05-01
Associate Director PV
PV12 - 16 million yen Tokyo Medical Device Marketing
- Company overview
- We are a global company in the pharmaceutical industry, engaged in research, development, manufacturing, and sales of pharmaceuticals. Our mission is to discover, develop, and provide innovative medicines to help patients with serious illnesses. As leaders in the future of the healthcare industry, we prioritize "Focus, Innovation, Compassion." We focus on disease areas with significant unmet medical needs and aim to guide people to new hope and contribute to improving their quality of life through the provision of innovative medicines and services.
- Responsibilities
- Responsible for pharmacovigilance and pharmaco-epidemiology deliverables including single case and aggregate safety monitoring, safety reporting, contribution to benefit risk assessment, risk management planning and strategy, and execution of certain post-marketing commitments and ensuring compliance with global regulatory requirements.
Martin Tsvetkov
Pharma -
Job number: JN -072024-36041 Posted: 2025-05-01
MSL(メディカル・サイエンス・リエゾン)※再生医療、オンコロジーの豊富な受託実績／年休128日
MSL・MA（メディカルアフェアーズ）経験者歓迎6 - 12 million yen Tokyo Pharmaceutical Medical Affairs
- Company overview
- Our client is providing drug development service.
- Responsibilities
- ■業務内容
医学的、科学的な側面から円滑なコミュニケーションを取り、KOL（Key Opinion Leader）と良好な関係を構築する。
臨床研究や製造販売後調査の立案・作成に関するサポートを行い、そのデータのPublicationを通じて製品価値を高める。
社内・外の関連部署とコミュニケーションを取り、製品ストラテジーに沿った市販後に向けた活動の企画立案。
社内外において医学的、科学的な面から自社製品の適正使用を推進する。
営業部門に対する医学教育サポートなどを行う。
Patrick Chang
Pharma -
Job number: JN -072024-143287 Posted: 2025-05-01
[Osaka or Tokyo] Medical Writer of Drug Development
Great Company Culture8 - 14 million yen Tokyo Pharmaceutical Research & Development
- Company overview
- Our client is the Japanese subsidiary of a European CRO with over 100 offices and tens of thousands of employees worldwide.
We have a strong business foundation providing global drug development services and a vision to be a “Global Healthcare Intelligence Partner”. We aim to provide advanced drug development operations by combining our experience in drug development with technology that enables 100% virtual clinical trials.
As a partner to pharmaceutical manufacturers and bio-venture companies, we provide a wide range of support from clinical trials to regulatory filings and post-marketing activities. We can also provide a comprehensive range of services including regulatory affairs, pharmacovigilance, and medical writing.
We have a culture where employees work healthy and enjoy challenges, and have been awarded “World\'s Best Company” multiple times by Forbes, an American economic magazine. - 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 -
Job number: JN -022025-183975 Posted: 2025-05-01
海外子会社の経理
経理、財務、監査法人、コンサルティングファームでの業務経験をお持ちの方必見です6.5 - 10.5 million yen Tokyo Accounting & Finance Accounts Payable / Accounts Receivable
- Company overview
- Our client is a manufacturer of water treatment equipment and chemicals.
- Responsibilities
- 海外事業拡大に伴い、海外子会社管理の強化を目的としております。そのため同ポジションは海外子会社からの経理関係の管理全般を担当して頂きます。▼具体的には…海外子会社からの財務報告内容の確認、修正依頼、連結パッケージ作成
海外子会社経理部門とのコミュニケーション（出張を含む）
海外子会社の経理プロセス改善、各種ポリシー策定
海外子会社の内部統制の構築支援及び評価
海外M&Aに関する業務（会計・財務に関する事項に限る）
国際税務関連業務
その他海外子会社・海外事業に関わる経理・財務・税務業務全般
Hanako Arai
Corporate Services -
Job number: JN -072024-25210 Posted: 2025-05-01
FP&A | 管理会計・経営管理
日本にいながら日系海外現地法人赴任経験を活かしたい方は必見です！6 - 8.2 million yen Tokyo Accounting & Finance Accounting Manager
- Company overview
- We are a Japanese machinery manufacturer specializing in the production of fluid machinery such as pumps, compressors, and turbines. Our strengths lie particularly in products for industrial and social infrastructure applications, including water supply and sewage, energy, air conditioning, and environmental protection. With advanced technological capabilities, we actively expand into international markets and are highly regarded worldwide. Since our establishment, we have focused on innovation and quality, striving to develop products and provide services that contribute to the realization of a sustainable society.
- Responsibilities
- 半導体製造装置の製造販売を行う事業において管理会計を中心とした以下の業務をお任せします。
業務内容：
担当関係会社から提供される月次財務実績の内容精査（2社程を担当予定）
全関係会社の月次業績見通しデータの集計と分析を行い、関係者へ報告
Maria Nakata
Corporate Services -
Job number: JN -082024-171044 Posted: 2025-05-01
【東京】Corporate Real Estate & Services Manager
Seeking facility management/people management experience7 - 10.5 million yen Tokyo Support & Administration General Affairs
- Company overview
- We are a global leader in biopharmaceutical development based in the United States.
Our client is a CRO giant, offering a wide range of services supporting clinical trials at every and all stages. They also provide specialized services for biotech-related clinical trials, leveraging their unique technology and industry expertise.
Our services span the entire spectrum of clinical development, from planning and execution to monitoring and data management. Additionally, we offer advice on pharmaceutical regulation and market deployment, supporting clients through the process from drug approval to market entry. - Responsibilities
- Oversee the day-to-day facilities operations in the following areas.
Main responsibilities:
General maintenance Housekeeping and infection control
Mailroom service (receiving and dispatching)
Reception activitiesPartner with department heads to act upon space “Needs and Opportunities” and to maximize facility value.
Manage, organize and improve on-going building maintenance plan.
Supervise and ensure the effective and professional conduct of local facility activities.
Manage building access and security and ensure appropriate measures are in place to mitigate identified risks.
Oversee service desk tickets response, turnaround time and efficiency.
Project ManagementPlan, budget and schedule office moves and modifications including project management tasks.
People ManagementUndertake the full range of duties relevant to the leadership, management and development of directs reports to ensure that their performance meets and/or exceeds both the business and their own personal goals/objectives.
Maintain and encourage a positive, results orientated work environment, building partnerships and modeling teamwork, communicating to the team in an open, balanced and objective manner.
Handle formal staff review processes e.g. performance and salary reviews to corporate standards and timescales.
Manage and oversee departmental activities including appropriate staff resourcing and quality control with respect to time and cost.
BCP, Safety and Sustainability Responsible for BCP (Business Continuity Plan) – planning, implementation for assigned location.
Manage and oversee Health and Safety information to employees.
Overall responsibility for site safety and a healthy work environment.
Oversee and manage employee work permits.
Manage and promote environmental sustainability and recycling at the location.
Budget planning and Procurement managementProduce accurate annual operational budget in collaboration with appropriate key stakeholders and provide input to senior management.
Manage facilities expense/spend to an optimal level to align with budget.
Reduce expenditure by cost saving initiatives, reforms and improving on processes and procedures.
Responsible and accountable for all Facility operational expenditure /expenses.
Partner with Procurement to enhance supplier relationships.
Drive engagement with vendors to reduce costs and maximize service delivery
Resource planning and forecasting Align with financial guidelines and ensure processes and procedures are followed.
Asset management Maintain and manage asset register at location.
Implement or maintain process/procedure for asset tracking and locating Retiring of assets
Lease management Key contact person between the Company and building management for assigned location.
Establish good working relationship between the Company and Landlord to improve communication, collaboration and problem solving.
Manage lease, identify key clauses pertaining to reinstatement obligation, renewal and notice periods, yearly escalations and lease expiration date.
Compliance & Integrity Compliance with FM & building related laws as required by statute.
Oversee and manage site compliance for all inspections/audits, regulatory or clients or statutory authorities.
Confidentiality Instill a culture of compliance with the code, company policies and all applicable laws
Nao Yoshida
Corporate Services -
Job number: JN -052025-187632 Posted: 2025-05-01
プロジェクトリーダー
製薬会社もしくはヘルスケア関連の研究において、創薬研究について３～４年以上の実務経験がある方必見です9.65 - 12 million yen Kanagawa Pharmaceutical Research & Development
- Company overview
- Our client provides integrated drug discovery research support services.
- Responsibilities
- 薬効薬理部門の代表として社外や社内他部門のメンバーで構成される医薬品候補創製プロジェクトチームに参画し、顧客やステークホルダーと議論・交渉の上、試験の立案・提案・実施をリードする。(35％）
自己免疫疾患やがん免疫などの免疫研究領域における試験の研究計画立案、試験実施、データ解析、報告を関係者とのコーディネートに、主体的に取り組む。（35％）
創薬などライフサイエンス産業に応用可能で有用な新規技術や研究手法、あるいは既存の研究機能の応用が期待される未開拓領域を探索し、事業化に導く。（20%)
国内外の学会・講演会等への参加をはじめ、戦略的に社内外の研究者およびステークホルダーとのネットワークを構築し、専門領域での人的ネットワーク 構築を図るなど、事業の拡大に向けた業務を担当する。(10%)
Martin Tsvetkov
Pharma