Jobs list

IR担当

上場企業におけるIR活動・広報実務経験をお持ちの方必見です

10.71 - 13.43 million yen Tokyo Sales & Marketing PR / Corporate Communications / IR

Company overview: Our client is an independent financial services group, focusing on Structured Lease and other business lines including; Banking, Securities, Real Estate and Advisory. The firm aims to services institutional and retail customers with various financial products and services utilizing their diverse range of financial services and products.
Responsibilities: 業務内容:
同社は、お客さまの夢の実現に貢献するファイナンシャルパートナーとして、お客さまの課題を解決する多様な金融商品・サービスを提供する、東証プライム市場に上場している独立系金融サービス企業です。このたび、IR/広報活動を通じて多くのステークホルダーに、同社の魅力を一緒に広めていただけるチームメンバーを募集します。主な業務内容:
IR担当部長として、以下の業務をご担当いただきます。投資家対応（決算説明会、投資家ミーティング、海外IR、問い合せ対応等）
決算関連資料の作成（決算説明資料、アニュアルレポート、株主通信、株主総会資料、等）
ホームページ運営
広報活動（プレスリリース作成、テレビＣＭ企画/制作、スポーツ振興支援（スポンサーシップ対応）、等）

PMI推進マネージャー

財務会計に関する基本的な知識がある方必見です!

8 - 12 million yen Tokyo Accounting & Finance Business Planning / Corporate Strategy

Company overview: We support the business growth of our group companies and manage their operations. Aiming to make "the lives of people around the world more enjoyable," we are building a global entertainment network. We operate amusement facilities and karaoke chains across the country, and we also engage in a wide range of entertainment businesses, including character merchandising, food and beverages, and content and promotions (such as movies and interactive content). We have expanded not only domestically but also to North America, China, Taiwan, the UK, and the Middle East, aiming to increase the overall amount of joy circulating in the world.
Responsibilities: PMIを見据えたPre-M&A業務（主にデューデリジェンス）への関与
M&Aによりグループジョインした会社のPMIの実行
担当会社のPMIチームの統括者として、ジョイン後100日プランの策定・実行・モニタリング
コーポレート部門の統合をメインに、GENDAおよび担当会社の経営陣や管理部門との調整・連携を行い、連結グループへのスムーズな加入を推進

Medical Affairs PM

Medical PM

8 - 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
Industrial & Life Science

Medical Manager

Strategy planning and data gathering

13 - 17 million yen Tokyo Pharmaceutical Medical Affairs

Company overview: We are a foreign pharmaceutical company. Through a merger with an international biopharmaceutical company, we have introduced innovative biotechnology to the Japanese market. Through highly specialized medical information activities, we are enhancing our presence in the Japanese market. Focusing on cancer, cancer immunotherapy, and infertility treatment, we provide innovative healthcare solutions to the people of Japan.
Responsibilities: STRATEGY:
Act as Local Medical Affairs TA expert in one or more TAs
Support the Brand or launch teams/ Local TA leadership team in the development of TA, Launch and Brand strategies
Lead Medical Affairs activities in assigned territory along defined local Medical Launch / Brand strategies
Consolidate and communicate trends, market insights, and unmet needs identified in the field

OPERATIONS:

Develop Medical material, review marketing material, trainings
Ensure scientific and clinical accuracy for specific product or brand
Receives adverse event reports and transmits such reports internally according to Company procedures
Ensures timely completion and up-to-date knowledge of Company policies / SOPs, and local laws and regulations
Maintains up-to-date GxP knowledge by following internal and external trainings
Conduct Local internal scientific training and ensure continuous Medical education of existing teams and new employees working in the Local TA
Develop Medical KTL development plans
Positively impact external perceptions and knowledge regarding company and company products
Maintain and demonstrate comprehensive and in-depth scientific TA knowledge when executing assigned tactics
Ensure operational excellence by sharing best practices
Map treatment landscape and medical environment for new indications/ programs
Provide support in the planning and tracking of the (TA-specific) medical budget

DATA GENERATION AND DISSEMINATION:

Lead/ support (depending on nature of study) Medical studies, assist to coordinate Local clinical projects and contribute to site selection for clinical projects
Lead Local publication process, publication dissemination and alignment with Local, Regional and Global publication plan
Act as a resource, liaison and facilitator for ISS and investigators that are aligned to the Medical Affairs strategy
Coordinate with ClinDev and ClinOps in providing field support for research studies and assist in the selection of clinical study sites
Assimilate, process and share medical information with stakeholders

STAKEHOLDER ENGAGEMENT:

Provide training to HCPs and support in realising Medical educational events
Interact with Local stakeholders in Medical community in TA
Identify and interact with influential members of the Medical community (HCPs/external experts) and other healthcare stakeholders (managed care organisations, government organisations, patient groups) within assigned territory and TA
Represent company at Medical Education events, programs, meetings and support patient advocacy related activities
Partner with external stakeholders to develop innovative solutions
Engage with internal colleagues (Medical Affairs department, Clinical Operations, Commercial colleagues as appropriate, etc.) in developing and delivering and participating in Medical or cross-functional initiatives

マーケティング分析＆パフォーマンスマネージャー

ビジネス分析、KPI設定、パフォーマンス管理及びレポーティングに関してのご経験と専門知識をお持ちの方必見です

10 - 12 million yen Tokyo Accounting & Finance Business Planning / Corporate Strategy

Company overview: We are a leading insurance company operating in Japan. We offer a wide range of insurance products and provide non-life insurance services to individual and corporate clients. We offer a diverse range of insurance products, including automobile, fire, and personal accident insurance, and provide plans tailored to meet the insurance needs of our customers. We emphasize high quality customer service and efficient responses, earning the trust of our clients. In addition, we are committed to stable operations and growth, leveraging our years of experience and expertise. With our leadership in the insurance industry, customer protection and satisfaction are our top priorities.
Responsibilities: 【職務目的】マーケティング＆コミュニケーション（M&C）部がリードするマーケティング活動の実行やそのビジネスインパクトの効果検証のために必要なデータの取得・測定・分析を支援することが主なミッションです。【職務内容】社内外の調査やデータを活用し、新規顧客の獲得、クロスセル、リテンション（顧客維持）イニシアティブを含むマーケティング活動の企画、実行、測定、最適化を促進するための手法やアプローチを開発し提供する。
主要なビジネスゴールの達成に向けた進捗を測定するパフォーマンスダッシュボードの設計、開発、運用、改善をリードする。
日本のパフォーマンスとビジネスインサイトのグローバル本社へのレポーティングをサポートし、他の地域とのベストプラクティスとノウハウの積極的な交換を行う。
デジタルチームと連携し、マーケティングKPIを効率的にモニタリングおよびレポートするための標準化されたフレームワークとプロセス（SOP）を導入する。
デジタル広告のパフォーマンスの効率的な運用および最適化および専門知識とSOPを活用したチームのKPI達成や顧客体験の向上をサポートする。
必要に応じてシニアマネジメントへのプレゼンテーションの実施やそのイニシアティブについてのフィードバックを得る。
M&Cメンバーのデータ分析やKPI管理能力の向上に向けた取り組みをサポートする。等

【東京】アンモニア向け大型低温タンク設計のリードエンジニア

大型低温貯槽の設計経験者必見です!

9.4 - 13 million yen Tokyo Industrial Electrical Engineer

Company overview: We are a comprehensive heavy industrial manufacturer operating in a wide variety of industrial fields. We primarily provide products and services in the aerospace, defense, energy, plant, and social infrastructure sectors. Leveraging our engineering capabilities and technological innovation, we design and manufacture advanced machinery and systems, contributing to the sustainable development of society. In addition, to address environmental issues, we are actively promoting the use of eco-technologies and renewable energy to solve the problems of society as a whole.
Responsibilities: 大型LNGタンク（海外案件が主）/大型アンモニアタンク（国内案件が主）いずれかの新規設計プロジェクトに初期段階から参画し、顧客やプロジェクトマネージャーとの協議を通じて仕様を決定
各大型低温貯槽の基本設計・詳細設計（約1.5年間程度の設計期間となり、基本的には1案件を担当）※組立図まで作成し、その後は関係会社へ設計外注。
エンジニアリングマネジメント（マイルストーン・設計スケジュール等の管理）
ステークホルダー（顧客、調達部門、建設部門など）とのコミュニケーション※海外案件では、顧客先へ月1回程度のマンスリーミーティングが発生します。また、設計不具合等があった場合はスポットでサイトへ出張することがあります。

Shotaro Tsubaki
Industrial & Life Science

電気・計装エンジニアリング

エンジニアリングやプロジェクトのマネジメントを行った経験をお持ちの方必見です

10 - 15 million yen Tokyo Energy / Environment / EPC (Oil & Gas) Electrical Engineer

Company overview: We are a comprehensive heavy industrial manufacturer operating in a wide variety of industrial fields. We primarily provide products and services in the aerospace, defense, energy, plant, and social infrastructure sectors. Leveraging our engineering capabilities and technological innovation, we design and manufacture advanced machinery and systems, contributing to the sustainable development of society. In addition, to address environmental issues, we are actively promoting the use of eco-technologies and renewable energy to solve the problems of society as a whole.
Responsibilities: 所有する欧州の最先端の技術を活用し、製鉄・非鉄・高炉業界におけるカーボンニュートラルを達成するための電気・計装設計およびマネジメントをお任せいたします。長年にわたる実績に裏打ちされた高い品質・技術水準、世界で培われた多彩な製品群等を強みとして、顧客のカーボンニュートラル実現に向けたスケールの大きな業務に携わることができます。

【豊洲】製鉄プラントのプロセス設計※カーボンニュートラル／製鉄・鉄鋼業界向け

燃焼・触媒関連の実務経験をお持ちの方歓迎

10 - 15 million yen Tokyo Energy / Environment / EPC (Oil & Gas) Process Engineer

Company overview: We are a comprehensive heavy industrial manufacturer operating in a wide variety of industrial fields. We primarily provide products and services in the aerospace, defense, energy, plant, and social infrastructure sectors. Leveraging our engineering capabilities and technological innovation, we design and manufacture advanced machinery and systems, contributing to the sustainable development of society. In addition, to address environmental issues, we are actively promoting the use of eco-technologies and renewable energy to solve the problems of society as a whole.
Responsibilities: 世界最大の製鉄プラントエンジニアリング会社のグループ会社（一貫製鉄所の製銑設備の設計・供給における世界トップ企業）と同社の合弁会社として設立された同社において、グループ会社が所有する欧州の最先端の技術を活用し、製鉄・非鉄・高炉業界におけるカーボンニュートラルを達成するためのプロセスエンジニアリングをお任せいたします。高い品質・技術水準、世界で培われた多彩な製品群等を強みとして、顧客のカーボンニュートラル実現に向けたスケールの大きな業務に携わることができます。
鉄鋼業界では、カーボンニュートラルの達成に向けた電炉への切り替えやCCS/CCUSなどの技術開発が積極的に取り組まれている中、現在ではそれらの技術を活かした新しい設備の導入等が進むフェーズとなっています。リードエンジニアとして、国内の製鉄・製鋼企業を中心とした高炉代替としての電気炉設備導入やカーボンニュートラルに関わる設備など最先端の技術を活用したプロセスエンエンジニアリングをお任せいたします。同社とグループ会社みならず、その親会社であるドイツグループの先進設備も取り揃えており、それらの製品・技術を用いて顧客へ幅広い技術提案を進めて行きます。案件はFSから参画し、世界をリードする技術を活かした高クオリティかつコストミニマムな設計提案を顧客のニーズに合わせて行います。プロセスの基本設計はヨーロッパで行われており、ヨーロッパの技術者とコミュニケーションを取りながら顧客からの要求仕様を検討し、合意形成を進めて行きます。その後は同社製品の顧客向けローカライズを含めた仕様への落とし込み、設計とその取りまとめを担当いただきます。据付・試運転・性能試験フェーズではSVとして試運転の指揮を行うこともあり、その際は数か月の出張が必要に応じて発生することがございます。
製鉄業界の二酸化炭素排出量は他産業と比較すると多く、脱炭素技術については欧州で盛んに研究開発が行われており、一部の技術すでに商用プラントへの適用が始まっています。ヨーロッパ由来の技術と同社由来の技術を組み合わせて、カーボンニュートラルを達成するための様々な課題解決に向けた設計業務に携わることができます。

【四日市】生産計画・生産管理（SCM）シニアマネージャー

福利厚生◎／車通勤可

11 - 16 million yen Mie Industrial Plant Manager

Company overview: Our client business activities: Development and production of NAND flash memory, sales of flash memory products
Responsibilities: 【年間休日130日・土日祝休／福利厚生◎／車通勤可／半導体企業である当社のメモリ製品は世界シェアトップクラス】
■業務内容：サプライチェーンの観点からアウトプット見通しとサイクルタイム分析
新品種立ち上げ時の生産計画を策定・実行
在庫数の分析及び見通し作成
米国本社との間での工場ウェーハの生産計画・生産管理業務
生産データを用いたアウトプット見通しとサイクルタイム分析
新品種立ち上げ時の生産計画業務
ウェーハ在庫数の分析及び見通し作成
半導体生産工場の稼働状態の監視、分析
Industrial Engineerが担当するシステムの改善プロジェクトをリード

■備考：出社ベース
部下有（少人数）
年間休日130日
完全週休2日制

財務管理(マネージャー)

予算予測、会計、報告書作成などの関連業務のご経験をお持ちの方必見です

8 - 15 million yen Tokyo Accounting & Finance Financial Accounting

Company overview: We are a leading ICT solution provider offering a wide range of ICT products and services. We provide services ranging from telecommunications equipment, computer networks, and cloud services for general consumers to solutions for telecommunications operators and enterprises.
Responsibilities: 部署のエンドツーエンドの財務管理（予算計画、ローリングフォーキャスト、業務分析、リスク管理を含む）
定期的に分析レポートを発行し、ビジネスリスクや問題を特定し、財務に関する専門的なアドバイスを提供し業務の質を向上に貢献する。プロジェクト経営管理
概算や財務分析などのツールを活用してプリセールス営業チームの金額管理に参加し、財務リスクを特定し、ビジネス目標達成をサポートする。またビジネスモデルの設計。顧客の財務報告書分析を行い、高品質な契約の獲得を支援。また総合財務ソリューションの設計を担当予定。財務の観点から顧客関係の構築のアシスト。
ビジネスユニットのリスク（経営リスク、内部統制リスク、不正リスクを含む）に対して監督責任を果たし、経営リスクをコントロールし、財務報告データの信頼性を確保する

国際税務スタッフ

国際税務コンサルティングに関する実務経験をお持ちの方必見です

8 - 15 million yen Tokyo Accounting & Finance Tax / Treasury

Company overview: We are a group specializing in international and domestic tax and accounting consulting. To address the "increasing complexity of tax issues" due to annual tax law revisions, the "generalization of tax litigation" seeking proper taxation, and the "diversification of options" driven by globalization, we provide comprehensive solutions in all areas of taxation, including tax consulting, tax strategy planning and execution, and tax litigation support. Additionally, our strength lies in offering practical support that goes beyond tax issues, encompassing commercial taxation and accounting audits, thus providing an optimal business environment. In Japan, we deliver accounting consulting services that meet global standards, catering to the diverse needs of our clients.
Responsibilities: 【インターナショナルタックス(国際税務)】外資系企業を中心とした法人税等の申告書作成業務、決算書類や各種届出書の作成、月次税務レビューなど、業務は多岐に渡ります。海外の上場企業の日本子会社や日本支店も多いため、多国籍企業が国際展開する過程における税務アドバイスを求められることも多いです。また、外資系企業に対しては、海外への所得移転を防止する観点から、複雑な税制が設けられており、外資系企業向けの質の高い税務申告書の作成サポート、対日投資の際の国内法や租税条約に関するコンサルティング業務を実施します。
その他クロスボーダー取引の場面における日本及び相手国の税務インパクトを検討することで、ワンストップでの税務コンサルティング業務を提供します。
補足:
コンプライアンス業務（日系大規模法人、外資系企業）を中心とした英語×税務を活かしたキャリア形成が可能。また、特にインバウンドの国際税務業務が多くあり租税条約、特殊な国際税務領域など複雑な税務実務にあたることができます。その他クロスボーダーM&Aにおけるコーディネーション業務、タックスヘイブン税制対応など、国際税務アドバイザリー業務への関与機会があります。自らの知識・経験・行動でクライアントに貢献することはもちろん、組織やメンバーにもポジティブな影響を与える、次世代のリーダーを担える人材を求めています。

Pharmacoepidemiology Scientist

Position at global mega pharma with very strong pipeline

8 - 14 million yen Tokyo Pharmaceutical Data Management / Biostatistics

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: Responsible to lead safety observational studies as scientific lead and to deliver deliverables

 Responsible as a study owner of regulatory mandatory safety studies under GPSP (Good Post-Marketing Surveillance Practice)
 Demonstrate scientific leadership in safety observational studies, and ensure scientific level of study deliverables from pharmacoepidemiology perspective.
Define research questions, develop study design including statistical analysis plan based on research questions, evaluate and interpretate data (analyze in some cases)
Review and develop study report/publications.
Lead scientific discussion in cross functional team and in discussion with regulatory agency.
Collaborate effectively with global and Japan relevant functions and external partners (investigator, CROs) so as to deliver valuable evidence.

Support non-regulatory mandatory safety observational studies

Provide pharmacoepidemiology expertise to support non-regulatory mandatory safety studies.
Engage in study protocol, study report/publication development and ensure scientific quality from safety perspective in collaboration with relevant stakeholders.

Demonstrate pharmacoepidemiology expertise in safety related activities through product lifecycle

Provide pharmacoepidemiology expertise to support compounds in development, new product launches, and existing marketed products.
Contribute to Japan Risk Management Plan (RMP) development, periodic report development.
Review and develop query response to regulatory authority.
Demonstrate knowledge of relevant global and local regulatory requirements and practices
Understand the roles & responsibilities of the EU Qualified person for Pharmacovigilance (QPPV) and support QPPV to enable to fulfill all QPPV legal responsibilities.

Contribute to organizational RWE capability development

 Act as subject matter expert in the development and maintenance of the Safety Quality System and training tools/programs as they relate to pharmacoepidemiology.
Provide pharmacoepidemiology related trainings.
Support system/process development to enhance productivity or increase scientific quality.
Obtain up-to-date pharmacoepidemiology approach/knowledge

Manager, Bio-Statistician

Global Company

10 - 13 million yen Tokyo Pharmaceutical Data Management / Biostatistics

Company overview: This company is the world\'s leading pharmaceutical company.
Responsibilities: Provide scientifically rigorous statistical input into study design, statistical analysis plans, interpretation of statistical results, project development plans, regulatory issues and scientific and commercialization projects.
Provide planning, delivery and communication of statistical analyses, data presentations, and scientific reports (topline reports, clinical study reports, etc.), including clinical trial/PMS results, support for publication activities, scientific presentations, and support to responses to queries from regulatory authority.
Be accountable for study/PMS level and submission level statistical deliverables on assigned projects.
Develop effective collaborations with others within clinical teams, partner lines, external regulatory, industry, professional and academic organizations.
Ensure that all study/PMS and project level statistical activities are conducted in compliance with relevant regulatory requirements and standards.
Be up-to-date on SOP training and compliance with all SOPs as required based on the assigned curriculum.
Provide statistical input and leadership to cross-functional activities – collaborate with other statisticians, data managers, clinical programming colleagues – for assigned studies/PMS and regulatory submissions.
Ensure timeliness and quality of statistical deliverables according to project plans for assigned projects.
Comply with all statistics and quality processes and data standards that are applicable to statistical outputs, and support processes that require statistical input.
Communicate and collaborate with global statisticians on assigned projects.
Provide a strong statistical presence in regulatory and professional circles.
Participate in research on statistical methodology and its applications to clinical trials/PMS.

プロダクトマネージャー

PDM／プロダクトオーナーとしての実務経験をお持ちの方必見です

8 - 12 million yen Tokyo Sales & Marketing Product Marketing / Product Development

Company overview: We are a co-creative solution firm that integrates pig farming with technology to support comprehensive improvement in agricultural productivity and provide transparent and safe food supply. Our mission is to co-create a circular economy for pork through data utilization, constructing an ecosystem based on environmental resource consideration (low burden) and respect for dietary diversity, thereby enhancing the entire process of pork production and distribution. We leverage technology to realize a society where both meat-eating and non-meat-eating cultures are respected, addressing sustainability challenges while offering abundant choices and spaces.
Responsibilities: 業務概要:
グローバル展開するリードPDMとして、市場調査からプロダクト戦略策定、機能要件定義、PoC実施・効果検証までを一貫してリードし、事業成長とGHG削減を実現していただきます。業務詳細:
【市場、プロダクト戦略】米国、ウクライナ養豚市場の調査／顧客／競合分析
中長期ロードマップ策定
【プロダクトマネジメント】機能要件定義・仕様書作成
UI／UX、ソフトウェア、ハードウェア要件の優先順位付けとリリース管理
【導入・運用支援】パイロット／PoC 計画～実施、効果検証
現地トレーニングとサポート体制構築

営業部長／事業戦略の策定・販売戦略の推進等

土日祝休み／フレックス／在宅勤務可長期就労可能な安定環境

10 - 12 million yen Kanagawa Medical Device Sales

Company overview: Our client is a leading global supplier in the fields of life sciences and clinical research from Europe.
Responsibilities: ■業務内容：
セールスディレクターとして、売上への責任、戦略立案および実行、市場分析、人員の採用と育成を担っていただきます。

【変更の範囲：会社の定める業務】

■具体的な業務内容：
営業予算、売上や利益予測の達成を確保するため、ビジネスの戦略計画を準備、実施
マーケティングプログラムや新製品導入による売上の成長を推進
営業チームを指導し、目標達成を促進
主要顧客や販売代理店、関係機関とのコミュニケーション強化
重要なイベントの財務影響を監視し、対策を立案
業界や競合情報を把握し、社内関係者に報告、協議する
プロセス改善によるコスト効率向上
優秀な従業員の採用や育成により組織強化
顧客志向、結果重視の文化を醸成
各種カンファレンス、トレードショー、シンポジウムなどのイベントへの代表参加
顧客クレーム対応や既存、新規アカウントサービス提供
設備や資材の維持管理
指示された重要タスク処理や変化への生産的対応
安全、品質、規制に従う

海外連結・開示担当

監査法人対応経験が活かせます。

8 - 12 million yen Tokyo Accounting & Finance Accounts Payable / Accounts Receivable

Company overview: Our client is a leading manufacturer of pachinko and pachislot machines and game software in Japan.
Responsibilities: 連結決算業務統括
海外子会社管理
短信・四半期報告書・有価証券報告書・招集通知作成
その他財務経理部の特命プロジェクト

ITアーキテクト

金融産業の情報システム部門でのご経験をお持ちの方必見です

9.5 - 12 million yen Tokyo Information Technology Architecture

Company overview: We are a company focused on life insurance operations. We are particularly strong in cancer and medical insurance, offering insurance products to meet diverse needs. To support our clients\' health and livelihood, we emphasize prompt payment of claims and excellent customer service. We also strive to develop innovative products and improve our services, and have earned a reputation among many customers for providing reliability and peace of mind.
Responsibilities: ITアーキテクトとして下記業務をお任せいたします。アーキテクチャ・マネジメントにおけるアプリケーションセキュリティ領域をリードし、アプリケーションセキュリティ設計標準を策定
アプリケーションセキュリティ領域における設計や採用テクノロジーの標準化を策定
メインフレームにおける開発・テストプロセスの構築と、新ソリューションの選定・評価・導入・保守作業およびツール標準の策定
アーキテクチャ・マネジメントにおけるインフラストラクチャ領域をリードし、システム基盤（OS/MW）の構造を定義し、システム基盤領域の設計や採用テクノロジーの標準化を策定

Environment promotion and Chemical substance management

Leading pharmaceutical company

8 - 12 million yen Tokyo Support & Administration General Affairs

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: Formulation of the Group's Medium-Term Environmental Conservation Plan
Promote the PDCA cycle for the single-year plan to achieve the mid-term plan (promote the environmental management system)
Promotion of chemical substance handling management based on trends in global laws and regulations
Creation and management of SDS for chemical substances and support for risk assessment related to handling of chemical substances at sites
Audits of internal and business partners on environmental protection measures and handling and management of chemical substances
Planning and deployment of new plans based on the data of environmental conservation actvities.

業務プロセス変革リード

システムアーキテクチャ、ソフトウェア開発、統合、テスト手法に関して知識をお持ちの方必見です

8 - 14 million yen Tokyo Information Technology System Administrator

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: デジタル技術を用いた業務プロセスの自動化を通じた変革を推進する
社内外のステークホルダーと連携し、自動化に適したデジタル技術の実装を推進する
グローバルでの自動化ソリューション提供体制において、国内ITシステムオーナーとして、グローバルレポートライン上でサービス提供業務を推進する
複数の自動化プラットフォームのガバナンス管理、パフォーマンス確保を行う
プラットフォームのライセンス、インフラ使用状況、サポートコストの管理と最適化を行う
自動化ソリューションのKPI設定と効果測定を実施する
Process Design Document(PDD)の作成とガバナンスを担当する
グローバルおよび地域のOCMチームと連携し、変更管理を支援する

経営企画

グローバル製造業において、子会社管理業務または本社経営企画業務経験をお持ちの方必見です

8.6 - 13 million yen Tokyo Accounting & Finance Business Planning / Corporate Strategy

Company overview: We are a manufacturer and distributor of electronic components and materials. Our products include magnetic components and electronic devices and are used in a variety of industries and fields. Our products are made with advanced technologies and high-quality manufacturing processes, and are characterized by their reliability and performance, contributing to the advancement of society through the development of information and communication technologies and the improvement of energy efficiency. We are also committed to developing environmentally friendly products and promoting energy conservation to help realize a sustainable society. Our products play an essential role in all aspects of daily life and industry. We contribute to the development of society by continuing to provide innovative technology and outstanding quality.
Responsibilities: ERM委員会(委員長は、現在は経営企画を管掌する執行役員)の事務局として、全社のリスクマネジメントの推進(リスクシナリオの設定、各リスクオーナー部門へのリスク評価依頼と結果のとりまとめ、経営会議・取締役会への報告準備、リスクマネジメントに関する開示文書の作成)
評価の結果を踏まえたリスク対策の改善提案（本社組織の機構設計と経営陣への提案含む）

Jobs list of 8 - 17 million yen

IR担当

PMI推進マネージャー

Medical Affairs PM

Medical Manager

マーケティング分析＆パフォーマンスマネージャー

【東京】アンモニア向け大型低温タンク設計のリードエンジニア

電気・計装エンジニアリング

【豊洲】製鉄プラントのプロセス設計※カーボンニュートラル／製鉄・鉄鋼業界向け

【四日市】生産計画・生産管理（SCM）シニアマネージャー

財務管理(マネージャー)

国際税務スタッフ

Pharmacoepidemiology Scientist

Manager, Bio-Statistician

プロダクトマネージャー

営業部長／事業戦略の策定・販売戦略の推進等

海外連結・開示担当

ITアーキテクト

Environment promotion and Chemical substance management

業務プロセス変革リード

経営企画

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