1000万円～の求人一覧

ジョイントベンチャーを含む大型分析プロジェクトをリード

仕事内容

ミッション：
あらゆるデータとあらゆる分析技術を活用して、医療に最適な意思決定を適用する。

担当業務：
・担当事業の主担当として、分析設計、開発、示唆出しを行い、事業インパクトを創出します。
・グループ内の各担当者の問題解決パートナーとして、担当事業部の課題を解決します。
・ジョイントベンチャーを含む大型分析プロジェクトをリードします。
・中長期的な価値提供を行えるよう、分析ソリューションプロダクトを開発します。
・DSの人材育成や成果物の品質向上を目的とした分析基盤開発などのグループの生産性を向上させます。

応募条件

【必須事項】

・データ分析プロジェクトにおいて顕著な実績のある方
・PythonやRを用いた開発経験が2年以上ある方
・機械学習や統計に関する知識が豊富な方

【歓迎経験】

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】東京

年収・給与

700万円～1200万円　

臨床開発を中心に開発のマネジメントなど様々な業務に関われるポジションです。

仕事内容

臨床開発を中心に、開発品が承認されるまでのスケジュールマネジメントなど、社内外を巻き込みながら、幅広く実務推進をご担当いただきます。
PMDA、FDA、厚生労働省との面談など、外部とのやり取りも頻繁にございます。 その他、共同研究やライセンスアウトに向けた契約業務、知財管理など、ご希望に合わせて業務をお任せしていきます。

応募条件

【必須事項】

・理系（薬学・生物・化学等）の学部卒以上
・製薬メーカーでの臨床開発に関する経験がある方

【歓迎経験】

・CMCに関する知見がある方 ・サイエンスのプレゼンや論文の作成ができ、ライセンス候補先やCDMO、CRO等と対等に交渉をできる方
・医薬品のライセンスイン、ライセンスアウトに関わったことがある方
・事業開発やプロジェクトマネジメント領域におけるリーダー経験
・海外のベンダーや機関との交渉をハンドリングできる英語力をお持ちの方

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】神奈川

年収・給与

600万円～1200万円　

財務経理部門の次期マネージャー候補として、業務に取り組んでいただきます。

仕事内容

・会計データの入力、管理
・試算表、B/S、P/Lの作成、分析
・予算実績の管理業務
・固定資産の計上及び管理業務
・経理業務全体のプロセス改善
・国税対応及び税務申告書作成

応募条件

【必須事項】

・上場企業での経理経験をお持ちの方
・税務対応のご経験をお持ちの方

【歓迎経験】

・経理部門でのマネジメント経験（2～3名でも可）をお持ちの方

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】大阪

年収・給与

800万円～1200万円　経験により応相談

外資製薬メーカーにて顧客体験を最適化するデジタルマーケティングをご担当いただきます。

仕事内容

・Key Job Accountabilities:
This role ensures the seamless customer experience across channels by supporting the end-to-end process from ICP to campaign execution and measurement. If successful, this role will have a key contribution to ensuring that the right content is delivered through the right channel to the right customer segment to optimize the customer experience.

・Based on deep understanding of brand strategy, contribute effectively to integrated customer planning & execution and customer engagement strategy development in early assets.
As a core team member to assigned therapeutic areas, collaborate closely with asset teams to plan, and execute integrated customer plan.
Work effectively with Strategy & Insights department & within Customer Experience Excellence to support the business in deriving actionable customer insights based on channel engagement and performance analysis to inform the omni-channel engagement plan.
Understand IAP & ICP planning approach & process to be a valuable customer centric contributor.

・Identify opportunities for omni-channel campaigns or optimize omni-channel engagement to enhance customer experience linked to business goals.
Lead omni-channel campaign planning & development & execution by partnering with the business & supporting operational functions to plan & execute omni-channel campaigns based on customer insights and needs.
Support key operations such as content management, content production, campaign tracking, next best action & campaign analytics for successful implementation
Contribute as a valued business partner with digital marketing expertise towards development of business omni-channel engagement strategy and building of new digital engagement channels with customer experience as top of mind.
Actively contribute to ICP planning to shape customer engagement plan using data & insights.

・Optimize channel & content performance.
Work closely with cross functional team applying UX design principles in the form of best practice guidance to both channel & content to drive performance.
Lead the development of relevant campaign metrics that enable cross functional evaluation of campaign and channel performance.
Collaborate with analytics colleagues to evaluate omni-channel reports and develop business relevant insights and actions.
Lead cross functional campaign performance review meetings to identify opportunities to optimize engagement in near time.

・Collaborate with cross-functional teams to define & improve core capabilities to enable omni-channel engagement.
Understand core omni-channel processes & platforms to act as point of contact for business to support smooth and compliant operations.
Act as an ambassador for core omni-channel processes including campaign planning, editorial/content planning, content tagging, digital production & adoption of best-in-class digital engagement.
Identify & apply best in industry practices for omni-channel engagement by staying on top of current trends and competitive approaches.
Partner with the business to develop robust business requirements to inform channel improvements.

Key Contacts:
・The position would have various touch points across all levels including senior leadership, within group.
This position will work across a matrix organization and as a change agent, will need to effectively influence without authority.
Report to Head of Omni-Channel Effectiveness Group, Customer Experience Excellence Department, Human Pharma Operations Division

Interaction with stakeholders:
・Roles within Omni-Channel Effectiveness Group, Customer Experience Excellence Department, Human Pharma Operations Division
・Respective Business Units
・Brand Marketing, TA, Medicine teams
・Legal & Compliance
・Global counterparts
・External suppliers

応募条件

【必須事項】

・Prior experience in Digital Marketing or Product Marketing
Demonstrable experience with knowledge and experience of:
・Design, planning & delivery of omni-channel and / or digital marketing campaigns
・Website development including content management
・Email marketing campaigns including campaign management system(s)
・Measuring & reporting on campaign analytics & KPIs
・Modern web / digital design & UX principles
・Experience implementing CRM-driven marketing campaign automation process & platforms
・Project management (knowledge of Agile / Lean / Scrum is a plus)

・Understanding of the key channels, digital platforms for customer engagement planning & execution
・Deep knowledge of Global ICP planning requirements
・Strong experience in managing process and leveraging data & insights.
・Education: bachelor’s or master’s degree
・Ability to articulate requirements clearly.
・Strong stakeholder management, negotiation skills, influencing without authority.

・Prioritization skills
・Excellent communication skills both in Japanese and in English
・Japanese: Fluent/Native
・English: Fluent (CEFR B1)

【歓迎経験】

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】東京

年収・給与

600万円～1200万円　

大手外資系企業にてセイフティーフィジシャンを担当いただきます。

仕事内容

Accountabilities
As an expert of benefit/risk (B/R) profile, which are assessed by global BR team and aligned among global and local, engage to take safety assurance measures such as preparation of J-RMP, proper use of drugs and closely work with evidence/asset team by providing B/R knowledge and work with global team by inputting local needs/insight.
・Lead to prepare local Risk management Plans in response to Japanese specific requirements (e.g. country-specific format) and content in liaison with GPV functions.
・Implementation and progress of global risk minimization measures, lead to prepare local RMP development and implementation not only for the delegated asset (AT) but also other products as needed. Provide PV input and insights to local labelling documents and educational materials (e.g. SPC, PIL) in time and quality.
・Perform local safety data monitoring not only for the delegated asset (AT) but also other products as needed. Timely information of the respective PVWG Chairperson on any relevant new safety information received from local sources for group products or for products of the same class.
・Promote implementation of safety assurance measure such as proper use of drug, including preparation of guidelines for them in collaboration with stakeholders (e.g.LRA, legal &complaince)
・Perform Medical Quality Review of all fatal / life-threatening cases as needed and defines appropriate follow-up measures. Complete ‘fatal case investigation’ report as needed.

Manage health authority requests, potential safety issues and / or crisis management not only for the delegated asset (AT) but also other products as needed and together with global/local stakeholders.
Contribute to the PSPV Culture, Local PSPV Strategy & the establishment and maintenance of a high-quality local PSPV system, Review controlled documents (e.g. PV Working Instruction, PV Repository, applicable sections in PSMF annexes, local SOPs, etc.) also contribute to Japan initiatives to promote Patient Safety & Pharmacovigilance concepts and conduct PV trainings, where the training needs were identified, for internal and external customers.

To be ready for inspection and support to management of non-compliance
・Reporting of non-compliances as soon as becomes aware of the issue and Contribute to investigate non-compliances and associated CAPA (Corrective and Preventive Actions) activities. Take over CAPA Lead Function, if required.
・Establish and support local inspection readiness, participate in PV audits and PV/GPSP/GCP inspections.

Support the implementation activities to enhance PV compliance culture and PV awareness at local level of the organization in line with global recommendations
Proactively cooperation with Global PSPV on any upcoming new regulations or group processes to assess the local impact and their implementation within the team.
・Contribute to seting up/optimizing of local PSPV processes including the takeover of subtasks e.g. creation/revision of the related documentation (Standard Operating Procedures (SOPs), Local PV System Framework, KMed Assets, etc.)

Regulatory and / or Organisational Requirements
Excellent knowledge of applicable global, regional and local PV regulations, group processes and relevant GxP requirements.
Be compliant and acts within ethics at all times.

Job Complexity
The position requires extensive regulatory,scientific knowledge and balanced risk-based decision making. This needs to take into account needs and requirements of other functions, departments and units.

Interfaces
Local Medical Director, Global Patient Safety & Pharmacovigilance, MSG,CDMAs, LRA, MKT, SL, RWD
GRA, CD&O

Job Impact
Conduct and Establish internal/external collaborations by sharing best practices

応募条件

【必須事項】

・Medical doctor
・Experience as clinician
・1+years’ experience at Experience at pharmaceutical industry at medicine department
・Experience in the field of clinical development is highly preferable
・Substantial knowledge about local GVP/GPSP regulation and global GVP regulation.
・Knowledge and experience of preparation of periodic report/RMP/EPPV
・Knowledge and experience of performing signal monitoring
・Knowledge and experience of PJ management
・Experience on industry activities (e.g. participating working group across companies) (preferable)
・Excellent command of English language (toeic score more than 785)

Skill and Competencies
・Proactive and assertive attitude to establish team and networking
・Problem solving skill and crisis-management skills
・Analytical skills on industrial trend.
・Conceptual and strategic thinking
・Project management and decision-making skills
・Ability to mentor, coach and train others
・Proactive and assertive attitude with customer service orientation
・Excellent communication and presentation skills

Language skills:
• Japanese: Native
• English: Fluent
Required English speaking CEFR level : B2

【歓迎経験】

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】東京

年収・給与

900万円～1300万円　経験により応相談

大手外資系企業にて製造管理を担当いただきます。

仕事内容

＜Accountabilities＞
・担当領域（工程、ライン、試験・分析、エリア等）において、定められた手順で業務を遂行し、要求を満足させることが求められる。（安全・衛生・品質・納期・コスト）
・異常・逸脱発生時は、担当領域において原因分析を行い、是正確定後は、指示事項及びSOPに従い処理することが求められる。
・GMP関連書類（ルーチンの生産・QMSに関連した書類）を正確に作成することが求められる。
・担当領域におけるSOPの定期改訂及び新規SOPの素案を作成することが求められる。
・資産の維持管理が求められる。（整備・清掃・在庫管理）
・業務改善やBPEを推進することが求められる。
・ローカルプロジェクトに参画し技術的なサポートを行うことが求められる。
・他者に対して技術的指導を行うことが求められる。

応募条件

【必須事項】

・高等学校卒もしくは同等の能力と経験を有する者
・優れた対人スキル
・医薬品の製造管理に関する知識
・医薬品固形製剤の製造工程に関する知識
・医薬品の製造部門及び製品に関する実務経験　3年以上（多少短くても可）
・Japanese – Native　あるいは　Fluent
・English – 英語を使用したコミュニケーションは求められないが、アレルギーの無い程度であることは要件となる

【歓迎経験】

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】山形

年収・給与

600万円～1000万円　

大手外資系製薬メーカーにて心・腎・代謝領域（肥満症/MASH領域）のMSLを募集しています。

仕事内容

1 担当疾患領域における科学的な課題をサイエンティフィックエクスチェンジを通して解決し製品価値の最大化に貢献する
2 担当疾患領域に精通する医師/その他医療関係者からの研究サポートや医学的・科学的ニーズを満たすための情報を提供する

Related Performace Indicators
1 活動計画の立案 To build activity plan
・担当疾患領域に精通する医師を特定し、適切に改訂する
To identify physicians in the responsible therapeutic area and revise list accordingly
・担当疾患領域に精通する医師とのengagement planを策定する
To develop appropriate engagement plan for physicians in the responsible therapeutic area

2 Engagement plan の実行及びその記録
To record and excute engagement plan
・担当製品に関するインサイトを得るために、サイエンティフィックインタビュー/ サイエンティフィックエクスチェンジを実施する。また、そのための適切なコンテンツを作成する。また、学会等からの最新情報も含め得られたインサイトは戦略やアクションプランの策定のために関連部門と共有する。
To conduct scentific interview/scientific exchange in order to gain insight on responsible product and to create appropriate contents. Also, to share insight including latest information from congress, etc. with relevant departments to develop strategies and action plans
・ 担当疾患領域で企画、実施するアドバイザリボード組織化をサポートし、ミーティングを企画・実施する。
To support planning and organization of advisory board for execution in the responsible therapeutic area as well as planning and implementation of meetings
・ 医師と定期的なコンタクト/コミュニケーションをとり、製品ライフサイクルを通じて良好な関係構築・維持する。
To build and sustain positive relations with physicians throughout product life cycle via regular contact and communication

3 データ構築及び研究支援 To provide support for research and data building
・データギャップやアンメットニーズを埋めるために、実現可能性、科学的適切性、倫理性を考慮した新たな科学的データを創出する。
To create new scientific data in consideration of feasibility, scientific appropriateness and ethics in order to fill data gap and unmet needs
・要望に応じた臨床/非臨床の研究をリエゾンとしてサポートする Support clinical/non-clinical research as liaison based on reques

4. 顧客からの要望に応じた承認/未承認/適応外の科学的情報の提供
To provide scientific data on approved/unappro ved/off-label products based on customer's request
・医療関係者からの科学的質問、要望に応じた適切なコンテンツを作成し、担当疾患領域内で承認を得た上で適切に情報提供を行う。
To create appropriate contents based on request and scientiic question from medical personnel as well as to provide appropriate information on top of full approval within responsible therapeutic area

6. 行動規範・法令の順守 To comply with Code of Conduct / Laws and Regulations
・ 法規制や業界ルール（プロモーションコード、公正競争規約、個人情報、データ収集/保管など）、関連SOP を理解し、遵守する。
To understand and comply with regulations and industry rules (promotional codes, fair competition rules, privacy, data collection/storage, etc.) as well as relatedSOP
・グループ社員の自覚を持ち、社会規範、社内行動規範則って行動する。
To act according to social norms and company's code of conduct with full awareness as a responsible group employee

応募条件

【必須事項】

・Excellent communication with external and internal stakeholders.
・High reading cpmprehension of scentific literature and presentation skills.
・Agile and effective working style in a fast-paced and changing enviroment.
・Internal/External
ステークホルダーとのコラボレーションを促進する高いコミュニケーション能力が必要

※MRのみの経験でも可能（ただし大学病院あるいはKeyオピニオン担当経験者が望ましい）

【歓迎経験】

・Experience in medical affairs or medical science liason activities for Cardio-Renak-Metabolism related products is perferable.
・少なくとも３年以上の経験のあるMSLが望ましい
・糖尿病領域もしくは肝臓領域での経験者であるとなお望ましい
・製薬企業での開発品Launch経験があるとなお望ましい
・ライフサイエンス分野のPhD（博士）、MSc（修士）もしくは薬剤師が望ましい

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】東京、他

年収・給与

500万円～1100万円　経験により応相談

プロジェクトの範囲と要件について交渉・定義し、プロセス改善やテクノロジーを活用したソリューションを提案

仕事内容

The Senior Principal System Analyst in IT GFS SCM & 3PM Commercial Order Management is responsible for delivering demand management, business consultancy, project management, and IT-related services to designated business stakeholders globally with focus on the APAC region including Japan. This role demonstrates strong capabilities in both project management and domain architecture.

Through continuous engagement with business partners, the analyst identifies and analyzes business needs, negotiates and defines project scope and requirements, and recommends process improvements and/or technology-enabled solutions. The role leads and manages IT projects end-to-end, ensuring alignment with business goals and strategic priorities.

Key responsibilities include：
Partnering with clients to prioritize and govern IT service demands.
Ensuring accountability for the delivery and performance of IT services.
Driving projects to achieve intended business outcomes and measurable benefits.
The successful execution of these responsibilities is expected to contribute significantly to overall business performance.

Additionally, the analyst collaborates closely with IT colleagues and business users to implement IT processes and technology solutions that enhance operational efficiency and productivity.

応募条件

【必須事項】

・5 years+ IT and business experience in the SAP Order-to-Cash (SD module) including documentation and testing
・Accomplished communication and relationship-building skills – you’ve worked with decision-makers, consultant resources and external creative and technical personnel, preferably in a fast-paced and complex project environment
・Proficiency in both Japanese and English

Ability to manage tasks independently
・Experience participating as a team member in projects

【歓迎経験】

・Experience in JIRA & Confluence (Atlassian suite) would be useful, but not essential
・Experience in project management (optional)

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】東京

年収・給与

600万円～1100万円　経験により応相談

医療用機器メーカーにて生産技術の管理職候補をお任せします。

仕事内容

幅広く生産技術業務をご担当頂きます。ご入社当初は強みの技術を活かして頂き、将来的には幅広い業務をお任せ致しますので、徐々に知識・技術を深めて頂くことを期待しています。
※以下のような業務をご経験や強みに応じてご担当頂きます。
（1）生産工程の設計
（2）生産設備の設計（機械・電気・ソフト）
（3）機械工作法、品質管理法、樹脂設計における金型構造の理解
（4）設備メンテナンス　等

応募条件

【必須事項】

・生産設備設計の実務経験(5年以上)
・CAD使用経験（2D/3D問いませんが、solid works経験があると尚可）

【歓迎経験】

・マネジメント経験or マネジメントに興味・意欲のある方

【免許・資格】

特になし

【勤務開始日】

応相談

勤務地

【住所】大阪

年収・給与

800万円～1000万円　

医療機器（クラスⅠ～Ⅲ）の薬事業務をご担当いただきます。

仕事内容

・医療用機器具の新製品の薬事申請
・改正薬事法対応
・市販後安全管理に関する業務(安全情報の収集、安全措置の立案）

応募条件

【必須事項】

・薬事経験をお持ちの方（目安2年以上）
・マネジメント・管理職経験をお持ちの方

【歓迎経験】

・英語力あれば尚可

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】大阪

年収・給与

800万円～1000万円　

医療機器メーカーにて自社アプリの開発をご担当いただきます。

仕事内容

医療機器と接続するユーザー向けの汎用デバイスアプリ（Android）の新機能開発をしていただきます。またご経験に応じてプロジェクトのリーダーもお任せいたします。仕様検討から上市後のフォローまで全工程に関与し、患者様の輸液管理をサポートするアプリの開発に主体的に関わっていただける方を募集しています。
・担当フェーズ：仕様検討～上市後のフォローまで全工程に関わっていただきます。
・開発言語：C#,Kotlin,PHP(言語)、Xamarin(フレームワーク)、Git(バージョン管理ツール)、Backlog(PJ管理ツール)
アプリと連動しており、患者様の術後疼痛に応じて輸液の投与状況をコントロール・管理することができる持続注入器。
※現在構想中の新商品開発にも携わっていただきます。

応募条件

【必須事項】

・モバイル端末向けアプリ開発やwebアプリ開発のご経験をお持ちの方
・マネジメント/リーダー経験をお持ちの方
・大学院、大学、高等専門学校卒以上

【歓迎経験】

・組込ソフトウェア開発経験
・Xamarinを用いた開発経験
・外国語アプリの開発経験
・ GitまたはTIマイコンまたはバックログ等のインフラ環境での開発経験

【免許・資格】

特になし

【勤務開始日】

応相談

勤務地

【住所】大阪

年収・給与

750万円～1000万円　

社内外の品質監査や製品試験の評価方法を開発し、品質向上意識を高める管理職クラスの人材を募集します。

仕事内容

・規制要求を踏まえた社内QMSの構築、維持改善
・設計開発～市販後段階までの品質保証、リスクマネジメント業務
・外部製造委託業者や供給者に対する品質監査
・製品試験における評価方法の開発、品質管理
・社内品質向上意識の醸成
＊出張頻度：国内→約4回／年、海外→約4回／年（監査員となった場合の最大）

応募条件

【必須事項】

・ISO9001又はISO13485取得企業で開発／品質保証／品質管理業務の3年以上
・英語力（目安：TOEIC(R)テスト600点以上）
・マネジメント/リーダー経験をお持ちの方

【歓迎経験】

・医療機器メーカーでの設計開発経験
・QMS監査受審対応／外部監査実施経験
・試験評価業務経験

【免許・資格】

特になし

【勤務開始日】

応相談

勤務地

【住所】大阪

年収・給与

700万円～1000万円　

医療機器メーカーでMSLを担当していただきます

仕事内容

The Medical Science Liaison (MSL) is a field based key position within organization. The position will be responsible to develop　relationships within the medical/scientific community, provide
medical and/or scientific data about products and research to healthcare professionals and support the HCP to enable the care of patients with Tumor Treating Fields (TTFields) in particular with
regards to patients with glioblastoma, and other indications in the future. Additional responsibilities include but are not limited to serving as scientific interface between company and the healthcare
professional communities with respect to communicating about clinical development plan and other research and development plans. To develop teaching materials as appropriate, facilitate
investigator sponsored trials(ISTs) on marketed and investigational indications and provide
perspective related to field activities associated with growing existing products and bringing new indications to market, are further responsibilities of this position. The MSL collects insights from Key
Opinion Leaders (KOLs) and shares them within the Company. The MSL also analyze those insights and contribute to the development of Medical Strategy. The MSL will take an important role on the　team, serving as a resource and mentor to field team members. The MSL will be responsible for the education/certification of new prescribers. Medical and scientific expertise will be maintained through
review of scientific literature, attendance at assigned medical meetings and self-learning. The MSL will work closely with cross-functional partners including Japan Business Team.

・Increases therapy awareness amongst prescribers and non-prescribers.
・Manages his/her territory and associated field-based activities.
・Performs activities related to marketed and research products including:
・Healthcare provider education on our products and disease awareness
・Facilitation of ISTs under local regulation appropriately
・Providing HCP’s feedback/insights and competitive intelligence to the company　regarding the therapeutic area and our products
・Attendance and coverage at assigned Medical Meetings, Organization of advisory boards, etc.
・Facilitate advancement of the body of science regarding TTFields.
・Supports therapy with TTFields through medical communications, scientific support for promotional activities and other related medical activities including, but not limited to studies, trainings, and medical information.
・Develops, maintains and extends contacts with national experts and medical professionals in our field of therapeutic area in particular regarding Oncology.
・Ensures 100% compliance with all applicable Standard Operating Procedures, local and international rules and regulations.

応募条件

【必須事項】

・Professional degree in natural science, medical or technical field
・Advanced scientific or health related degree preferred, i.e. PhD, Pharmacist (PharmD or RPh), Medical Doctor (MD), or other clinical/scientific experience
・Combined oncology and industry experience is a strong plus
・Experience in a similar role is a plus

・Must have excellent oral and written communication skills; strong presentation skills
・Must demonstrate fluency in articulating scientific concepts and data
・Excellent interpersonal skills
・Must have good judgment, ability to adapt and change in a shifting environment
・A strategic, passionate, self-starter who takes initiative
・Detailed oriented, highly organized and highly flexible
・Must be self-directed and able to complete projects with limited supervision
・Must work well in large and small teams, ability to work remotely
・Ability to travel ＞80% time
・Comfortable with occasional after-hours and weekends availability
・Autonomous, hands-on, and open mind set
・High ethical standards
・Prescriber focus oriented: bring expertise and innovation and collaborate with the prescriber
・Solid working knowledge of Microsoft office (word, excel, PowerPoint) and Outlook
・Japanese: Native level fluency is a must
・English: Business-level English skill preferred.

【歓迎経験】

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】東京

年収・給与

600万円～1000万円　経験により応相談

内資製薬企業にて、知的財産マネージャーを募集しています。

仕事内容

・日用品の知的財産関連（主に特許、意匠）の国内および海外の業務全般について、実務担当者として中心的な役割を担います。
・国内、海外の製品展開における知財リスクの評価・判断
・グローバル知財マネジメント（事業部、海外拠点、研究開発部門との部門間連携・戦略立案）
・他社特許対応業務（侵害予防調査、鑑定、侵害リスク判断、情報提供、異議申立等）
・出願・権利化業務（先行技術調査、出願、中間処理、発明発掘等）

応募条件

【必須事項】

・事業会社における知的財産実務経験(5年以上)
・国内および海外(中国、東南アジア、欧米)の知財制度・法律の知識
・国内、海外の侵害予防調査、知財リスクの評価・判断の経験

【歓迎経験】

・国内外における知的財産権活用の経験
・国内外における模倣品対策の経験
・チームメンバーのとりまとめ、メンバー教育の経験
・英語力(海外文献調査や現地代理人とのやり取りが可能なレベル)

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】東京

年収・給与

850万円～1050万円　

全社的な予算編成・予測プロセスやIR報告において事業部門都連携や予算編成・予測プロセスをサポート

仕事内容

Responsibilities include liaising with all areas of the business to complete the enterprise-wide budgeting and forecasting processes (MTP/RBU/PB) and quarterly IR reporting (QBR); preparation of consolidated management reporting and analyses for regional Senior Management; reporting of total regional MTP/RBU/PB forecasts to both regional Senior Management and to the Group, and maintenance of the data collection and analysis tools within the Financial Planning and Reporting area.

The role broadly includes the following key components:
• Business Strategy & Decision Support; supporting key business & investment decisions with solid skills in scoping customer requirements, analysing issues, developing options and enabling appropriate decision making based on strategic business need
• Business Performance: driving financial performance and business activity, to deliver and communicate performance and business planning submissions/reporting, and to advise senior management on key drivers.
• Contribute the completion of the enterprise-wide planning cycle for the country.
• Responsible for ensuring financial and management data collection tools operate effectively and efficiently to support the budgeting and forecasting process.
• Liaise with the business partners to ensure the financial planning and reporting systems operate properly and key financial reports are accurate.
• Lead for country MTP/RBU/PB submission in Hyperion Planning ensuring P&L and underlying sales and expense detail are accurate. Ensure linkage between regional budget data collection and UK reporting requirements. Serve as Liaison with Group Finance.
• Responsible for preparing and analyzing in depth financial and business performance analyses of budgets, forecasts and actual results for review by Senior Management.
• Responsible for obtaining a solid understanding of key business drivers, risk factors and industry trends and applying this knowledge to financial analyses.
• Identifies and implements continuous improvement opportunities to the planning and monthly reporting processes.
• Performs ad-hoc reporting requirements and financial analysis.
• Continuous Improvement, Coaching & Governance; supporting continuous improvement in Finance processes and capabilities and to help financial risk management and financial governance in area of accountability.

応募条件

【必須事項】

・B.S. Degree in Finance or Accounting or equivalent knowledg
・Experience of working within a multi-disciplinary team and liaising with senior managers
・ Demonstrated ability to perform in an environment that emphasizes teamwork
・ Demonstrated ability to lead a process/ project management/ problem solving with minimal or no supervision with strong self-leadership capability
・Excellent PC skills and experience including Oracle Hyperion Planning including Smart View, SAP, Excel and PowerPoint.

語学：
日本語 Japanese：Fluent Level (verbal and written)
英語 English：Business Level (verbal and written)

【歓迎経験】

・ Experience of working in a multi-national pharmaceutical company
・Experience of working in global/regional organisation / understanding of the drug development life cycle and/or commercial aspects, Accounting knowledge
・Experience of Finance Business Partnering, Accounting
・ Good cultural awareness, exposure to global working

【免許・資格】

<必須 Mandatory>
・Qualified finance professional (or equivalent)

<歓迎 Nice to have>
・USCPA
・JCPA
・MBA

【勤務開始日】

応相談

勤務地

【住所】大阪、他

年収・給与

1000万円～1400万円　

大手製薬企業にてポートフォリオのベネフィットを一人でも多くの患者さんに届けサイエンスの価値を最大化

仕事内容

・市場環境、顧客、製品およびポートフォリオを深く理解し、ブランドチーム、関係部門などと協力しながらビジネス課題を特定・構造化・分析し、課題を解決するための製品戦略を立案する
・製品戦略に基づく実行プランの一部(主にコンテンツ作成・イベントなど）を立案・実行・評価まで責任を持って実施する
・リサーチャーと共に、市場環境の正確な理解、戦略立案のための仮説の検証、打ち手の評価を一次・二次調査により明確にし戦略の検証・改善を行う
・戦略の立案・実行に際して社内外のステークホルダへ提案し、承認・サポートを獲得する
・営業部門を始めとする他部門とのコミュニケーション、社外医学専門家のマネジメントを円滑に行い、戦略の実行を徹底する
・グローバルチームや他国と協力しながら日本に留まらない製品価値の最大化をサポートする

応募条件

【必須事項】

・医薬品業界でのマーケティング経験(特に自己免疫疾患、指定難病やバイオ医薬品における経験)
・市場調査の定量、定性情報に基づきビジネス戦略の立案と実行をリードした経験
・営業部門を始めとする他部門やKey External Experts (KEEs)と協力し、ビジネス戦略に基づいた活動をリードした経験

語学力：
・日本語：ネイティブレベル
・英語：英語でのビジネスコミュニケーション能力が十分であること(TOEIC 800点相当)

【歓迎経験】

・自己免疫疾患、指定難病、バイオ医薬品におけるマーケティング経験
・新製品上市の経験 (特にマーケティング）

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】大阪、他

年収・給与

700万円～1100万円　経験により応相談

日本拠点のITインフラストラクチャのあらゆる側面の計画、実装、保守、サポートを担当

仕事内容

・Oversee the day-to-day IT operations, ensuring smooth functioning of all infrastructure components including networks, servers, workstations, and telecommunications equipment.
・Manage the installation, configuration, and maintenance of hardware and software necessary for manufacturing and production (e.g., industrial PCs, control systems, printers, mobile devices).
・Ensure IT systems at the site adhere to global security standards, compliance policies, and data protection regulations, implementing access controls, patching, backup, and disaster recovery procedures.
・Monitor performance and health of critical systems, proactively addressing outages, bottlenecks, or issues impacting production or business continuity.
・Liaise and coordinate with central/global IT service teams and third-party vendors for implementation of new services, troubleshooting, upgrades, and technology refreshes.
・Maintain up-to-date documentation on site infrastructure, system configurations, network architecture, and support processes.
・Provide technical guidance, hands-on support, and training to site staff for hardware, software, and IT policies.
・Lead local IT initiatives and projects (upgrades, migrations, rollouts) and coordinate cross-functional teams for successful project delivery.
・Implement factory automation solutions and support integration with manufacturing execution systems (MES), process control networks, and industrial IoT platforms, as applicable.

応募条件

【必須事項】

・Bachelor’s degree in Computer Science, Information Technology, Engineering, or relevant field.
・Several years’ experience managing IT infrastructure in a manufacturing/industrial/large site environment.
・Strong technical background in server management (Windows/Linux), networking (LAN/WAN/Wi-Fi), Active Directory, and virtualization.
・Hands-on experience with endpoint management, cybersecurity, backup and recovery solutions, and troubleshooting complex IT issues.
・Familiarity with industrial IT environments, including automation/control systems, OPC, or SCADA systems, is highly desirable.

スキル：
・Technical Expertise：
Deep knowledge of network management (LAN, WAN, Wi-Fi, VLANs), server management (Windows/Linux), virtualization platforms (VMware, Hyper-V), and Active Directory administration.
・Hardware & Software Skills：
Proficiency in installation, maintenance, and troubleshooting of servers, workstations, industrial PCs, printers, mobile devices, and related peripherals.
・ Cybersecurity：
Understanding of cybersecurity fundamentals, firewall configuration, endpoint protection, vulnerability assessment, access control management, backup, and disaster recovery best practices.
・Industrial IT Knowledge：
Familiarity with operational technology (OT) environments, including automation, PLCs, SCADA systems, MES solutions, and Industrial IoT platforms.

【歓迎経験】

・Experience supporting OT (Operational Technology) environments, factory automation, or integration with ERP/MES systems.
・Certifications & Professional Development：
Holding or working toward certifications such as ITIL, CompTIA A+, Network+, Security+, Cisco CCNA/CCNP, Microsoft MCSA/MCSE, or comparable credentials.

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】東京

年収・給与

600万円～1200万円　経験により応相談

新薬上場、価格改定において、戦略的な価格設定を推進頂きます。

仕事内容

Lead Pricing Group to achieve successful pricing outcome for new drug listing and price revision.

・ Support group members’ activities and develop members’ capabilities.
・ Lead strategic price negotiationon responsible products with MHLW and manage preparation for the negotiation.
・Assess price potential of pipeline products under close collaboration with Market Access group.
・Contribute to business planning with insightful analysis on healthcare & pricing environment change through close monitoring of discussion at　Government councils and pricing tendency.
・Collaborate with other departments to gain support for optimal pricing based on pricing strategy.
・ Collaborate with Global Pricing & Market Access team in order to align the pricing strategy , and gain support from global team as needed basis.
・ Build strong relationship with MHLW officials and leverage it to mixmize pricing outcome.
・ Lead industry discussions on pricing system reform through trade association activities.

応募条件

【必須事項】

【経験 / Experience】
• Leading negotiations with MHLW in terms of new drug pricing.
• Working to develop assumpetions on new drug prices/price forecast on the future.
• Working with members from other companies on the activities in trade associations.
• Working in a multi-national pharmaceutical company.

【能力 / Skill-set】
• Excellnt knowledge of healthcare business and NHI pricing regulations in Japan.
• Interpersonal and communication / persuasion skills with ability to influence others without authority
• Strong analytical ability
• Strond leadership capability

【語学 / Language】
Japanese：Fluent Level (verbal and written)
English：Business Level (verbal and written)

【歓迎経験】

【経験 / Experience】
• Leading a team as a manager
• Experience of cost-effectiveness assessment
• Good cultural awareness, exposure to global working

【能力 / Skill-set】
• Excellent PC skills
• Clinical Development Knowledge
• Familiarity with operating in Global business

【免許・資格】

＜必須 / Mandatory＞
Bachelors degree in relevant field (Marketing, Science, Economics or pharmacists, etc.)

＜歓迎 / Nice to have＞
• Pharmacist license
• Medical license

【勤務開始日】

応相談

勤務地

【住所】大阪、他

年収・給与

1200万円～2000万円　経験により応相談

開発中の製品のプロジェクト戦略を策定・実行を担っていただきます。

仕事内容

・The Project Leader is a cross-functional project leader of relevant Project Team to build and execute project strategy (ies) of a development product(s), including NME project(s) and/or LCM project(s) which require clinical trial(s) in Japan
・The Project Leader provides the leadership to the project team(s) to build high performing team(s) for maximizing the value of product(s) in Japan
・The Project Leader is accountable for the responsible project strategy (ies), and is a single point of contact from the global team(s), and the relevant function in marketing company such as Commercial/Medical functions as well as external co-development partners where applicable

応募条件

【必須事項】

・Bachelor’s of Science in an appropriate discipline
・Extensive leadership and project management experience in multi-disciplinary drug development environment
・Experience and knowledge in drug development including study execution, regulatory interaction, and product launch
・Experience of radio pharmaceuticals (e.g. radiocondjugates) development

語学力：
英語 English： Business English
日本語: Native level

【歓迎経験】

・Doctor of Philosophy
・Experience on negotiation with PMDA/MHLW, and getting JNDA/sJNDA approval and supporting launch activities　　　　　　　　　　　　　　　　　　　　　　　　　　　　　　　　・Negotiation with external experts/stakeholders
・Drug development experience in outside of Japan

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】大阪、他

年収・給与

1000万円～　経験により応相談

高度な数理科学的専門知識を駆使し、革新的なデータサイエンスソリューションを開発する役割です。

仕事内容

The Associate Principal AI Scientist (Activity optimization lead) will direct the application of sophisticated quantitative expertise in advanced mathematical disciplines to develop innovative data science solutions. The role will drive the application of foundational and cutting-edge techniques to manipulate and process structured and unstructured data, in combination with business domain knowledge, to develop and apply advanced modelling algorithms (e.g. classification, regression, clustering, NLP, image analysis, graph theory and more) to generate business and scientific insights. They likely coordinate the creation, maintenance and/or improvement of advanced AI models for ongoing and ad hoc review and analysis. The role will work autonomously with limited direct supervision from senior team members. Will provide coaching, task management and support to Associate AI Scientists promoting best practice across multiple domains, and/or stakeholder groups.

応募条件

【必須事項】

• Basic SQL based data extraction.
• Develop Python based ML models using Scikit-Learn, Keras (or Tensorflow), PyTorch, PyG, and other related libraries.
• Ability to create documents to clearly explain complex architecture without using language for specialist.
• Providing Excel based data aggregation.
• Understanding business needs and objectives properly.
• Explaining complex analysis to non-analytical personnel.
日本語 Japanese：Business
英語 English：Business

【歓迎経験】

• Model deployment by use of SageMaker pipeline.
• Good cocommunication and logical thinking skill.
• Eagerness to absorb new, cutting-edge methods.

【免許・資格】

【勤務開始日】

応相談

勤務地

【住所】在宅可、大阪

年収・給与

900万円～1300万円　経験により応相談