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Senior Medical Director Therapeutic Area (Medical…

アステラス製薬株式会社
【Purpose Scope】 ・Accountable and responsible for development and implementation of a global medic…
1500万円~1800万円 / メンバー

取り扱い転職エージェント

  • 勤務地

    東京都

  • 仕事内容

    【Purpose Scope】 ・Accountable and responsible for development and implementation of a global medical development plan on a large complex late phase project or on a group of complex earlier phase projects. ・Serves as global medical lead (GML) on one or multiple Astellas Pharma Global Development (APGD) Core teams including late stage and complex projects. ・Responsible for designing and conducting a global medical program resulting in quality regulatory submissions. ・Responsible for the medical interface with research through regulatory authorities and the commercial organization. ・Provides medical leadership on the Global Project Team and chairs the Global Clinical Team meetings. ・Supports to other projects as required. 【Essential Job Responsibilities】 ・Accountable and responsible for design and final recommendations in clinical development plan for their drug (s) after soliciting appropriate input and review from colleagues within Regulatory Affairs Commercial and Medical Affairs (Global and Regional) Manufacturing Clinical Pharmacology Statistics Health Economics and Outcomes Research and other line functions. ・Leads the global medical team(s) to design implement and conduct multi phase development studies globally to support filing of successful regulatory submissions and supplemental filings post approval. ・Leads APGD medical programs when required as part of post marketing requirements. ・Accountable and responsible for execution and delivery of the clinical development plan (in conjunction with Global Development Project Leader (GDPL)). ・Acquires public knowledge of present and future competitor products and how they impact the internal medical and commercial strategy. ・Negotiates milestones and ensures clinical development objectives are met (in conjunction with Global Project Development Leader). ・Plans for resources required both within the Medical Sciences organization and in conjunction with the Global Development Project Lead (GDPL) and the Glob…

  • 応募資格

    【Qualifcations】 The candidate must be a strong physician scientist with several years of experience in the global pharmaceutical industry. Capable of designing and executing clinical development plans providing medical leadership to a project team and to junior medical staff providing clear updates on progress to milestones and strong medical and product development acumen to programs and the team. <Required> ・Medical Degree (or Medically Qualified) with post graduate qualification and specialization in the appropriate specific therapeutic area/or one of the groups preferred ・Should have at least 5 years relevant experience in drug development in a biotech/ pharmaceutical company or equivalent experience in an academic clinical research role(NCI NIH Academic Research groups etc) ・Proven record of being a successful medical leader and a study clinician. ・Experience managing drug development programs. ・Experience designing implementing and conducting clinical studies to produce both timely and high quality data. ・Proven ability to get results in a matrixed management environment <Preferred> ・Additional post doctoral training or additional qualifications such as PhD PharmD certificate in Pharmaceutical Medicine highly desirable ・Prior experience in leadership role in EU/US regulatory filing.

  • 転職エージェント

    株式会社 ジェイエイシーリクルートメント

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Medical Director Development (Medical Doctor On…

アステラス製薬株式会社
【Purpose Scope】 Accountable and responsible for development and implementation of a global medic…
1300万円~1600万円 / メンバー

取り扱い転職エージェント

  • 勤務地

    東京都

  • 仕事内容

    【Purpose Scope】 Accountable and responsible for development and implementation of a global medical development plan on an early to late phase project. Serves as global medical lead (GML) on early stage project or at the indication study level for a larger/complex/multi indication program. Responsible for designing and conducting a global medical program resulting in quality regulatory submissions. Responsible for the medical interface with drug discovery regulatory and commercial colleagues. Provides medical leadership on the Global Project Team and may chair the Global Clinical Team meetings; collaborates with other project team members and study team(s) to ensure delivery and quality of clinical trials. 【Essential Job Responsibilities】 Fulfills the role of Global Medical Lead (GML) and is a member of the APGD Core Team. Responsible for design and recommendations of the clinical development plan(s) after soliciting appropriate input and review from Medical and Clinical Operations colleagues as well as other contributing line functions (Regulatory Affairs Statistics. Clinical Operations Commercial). Leads the medical team for assigned clinical trials to design implement conduct and interpret clinical studies to support decisions to advance or halt development of a new drug or to successful filing regulatory submissions. Responsible for execution and delivery of the clinical development plan. Acquires publicly available knowledge of competitor products and clinical plans. Negotiates milestones and ensures clinical development objectives are met. Motivates global clinical team towards the common goal of submissions of approvable regulatory filings or next clinical milestone. Attends important meetings with the FDA PMDA and as needed with regulatory agencies worldwide. Contributes to Global Project Team meetings. Responsible for keeping GDPL other project physicians and VP Global Medical Science TA Head informed of clinical progress and any…

  • 応募資格

    【Qualifcations】 <Required> Medical Degree (MD) or Medically Qualified with post graduate qualification and specialization in appropriate therapeutic specialty preferred. Should have at least 3 years relevant experience in drug development at a biotech/pharmaceutical company or the equivalent experience at an academic clinical research (NCI NIH Academic Research groups etc. Significant and demonstrable working knowledge of regulatory procedures and guidelines in all regions (global scope). Proven track record in clinical study design monitoring and execution and results analysis. Has demonstrated knowledge of designing implementing and conducting clinical studies to produce both timely and good quality data. Proven record of working on teams and in a matrix environment. Proven ability to get results in a matrix management environment. <Preferred> Additional post doctoral training or additional qualifications such as PhD PharmD certificate in Pharmaceutical Medicine. Prior experience in leadership role in PMDA/EU/US regulatory filing. Experience in development and implementation of global clinical trials for the registration and support of NMEs worldwide.

  • 転職エージェント

    株式会社 ジェイエイシーリクルートメント

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最大手ファンダリーのMemory Design Engineer and Manager

非公開
700万円~899万円 / メンバー

取り扱い転職エージェント

圓山 孝一
  • 勤務地

    神奈川県

  • 仕事内容

    最大手ファンダリーのMemory Design Engineer and Manager*SRAM architecture design *Read and write critical path design and analysis *Design of key building blocks (sensing, analog, high voltage, DFT) *Chip-level design verification *Embedded non-volatile memory compiler and productization *Co-work with product/reliability engineer on silicon characterization and reliability qualification

  • 応募資格

    ◆学歴 ・大学卒以上 ◆経験・スキル *The candidates should have at least bachelor degree with 10 years of experiences, master degree with 3 years of experience or PhD degree in relevant field. *Memory experts in the field of SRAM. *Familiar with bit cell characteristics (Vmin, bit cell performance, write margin), sense amplifier design, high sigma variation analysis, race check, margin signoff. *Knowledge on high speed and low Vmin design is a plus. *English is a plus ◆英語スキル ・ビジネスレベル

  • 転職エージェント

    株式会社A・ヒューマン

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Senior DevOps Engineer<正社員>

非公開
お気軽にお問い合わせください。
1000万円~1200万円 / 管理職

取り扱い転職エージェント

  • 勤務地

    東京都

  • 仕事内容

    <Key Accountabilities> Design and develop CI/CD pipelines and process automation solutions. ・Design, implement and maintain the CI/CD pipelines and the components that support it. ・Maintain application environments with an aim towards automation. ・Design, implement and maintain solutions to support our infrastructure and configuration management (Kubernetes, AWS, etc.) Bridge communication between project managers, developers, and DevOps engineers. ・Communicate with project managers to collect the requirements for projects. ・Understand the technical implications of those requirements and communicate them to other DevOps engineers. ・Support other DevOps engineers in the implementation of the project requirements.

  • 応募資格

    <技術スキル、職務経験> ・Minimum of 5 years of experience in DevOps designing, implementing, and maintaining CI/CD pipelines. ・Minimum of 3 years of experience supporting orchestrated Dockerized applications (Compose, Rancher, Helm, Kubernetes, etc.) ・Minimum of 5 years of experience supporting applications on cloud platforms (AWS preferred) ・Advanced understanding about Linux, namespaces, Cgroups, SELinux, etc. ・Expertise with distributed systems from high-level diagrams all the way to processes, protocols and resources (CPU, Mem). ・Solid experience with automation and scripting (Python & Go are preferred) ・Good troubleshooting skills with Java and JavaScript based applications. <証明書、学歴> ・Bachelor’s degree in Computer Science ・Kubernetes Certification(s) or equivalent experience. ⁃ AWS Certification(s) or equivalent experience. ⁃ Professional experience on at least one programming or scripting language (Python & Go are preferred).

  • 転職エージェント

    キャリア・ネットワーク株式会社

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最大手ファンダリーのMemory Design Engineer and Manager

非公開
900万円~1099万円 / メンバー

取り扱い転職エージェント

圓山 孝一
  • 勤務地

    神奈川県

  • 仕事内容

    最大手ファンダリーのMemory Design Engineer and Manager*SRAM architecture design *Read and write critical path design and analysis *Design of key building blocks (sensing, analog, high voltage, DFT) *Chip-level design verification *Embedded non-volatile memory compiler and productization *Co-work with product/reliability engineer on silicon characterization and reliability qualification

  • 応募資格

    ◆学歴 ・大学卒以上 ◆経験・スキル *The candidates should have at least bachelor degree with 10 years of experiences, master degree with 3 years of experience or PhD degree in relevant field. *Memory experts in the field of SRAM. *Familiar with bit cell characteristics (Vmin, bit cell performance, write margin), sense amplifier design, high sigma variation analysis, race check, margin signoff. *Knowledge on high speed and low Vmin design is a plus. *English is a plus ◆英語スキル ・ビジネスレベル

  • 転職エージェント

    株式会社A・ヒューマン

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高給与・好条件の多くは未公開求人です

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最大手ファンダリーのDesign Methodology

非公開
1000万円~1199万円 / メンバー

取り扱い転職エージェント

圓山 孝一
  • 勤務地

    神奈川県

  • 仕事内容

    最大手ファンダリーのDesign Methodology/Flow Development Manager & EngineerReport To: Director or Sr. Manager Role: *Digital Design Methodology/Flow Development for TSMC advance technologies. * Responsible for design/technology performance/power/area (PPA) analysis and optimization for TSMC advance technology nodes. * EDA tools Enablement & Certification * Customer’s design flow support Responsibility: * Design/Technology PPA analysis and optimization * EDA Tool Enablement & Certification *Customer’s design flow support

  • 応募資格

    ◆学歴 ・大学卒以上 ◆経験・スキル Requirements: *Education: - M.S. degree or above in EE/CS * Minimum of 3+ years of working experience in digital design, design flow & chip implementation related field. * Familiar with APR tools (such as Cadence Innovus and Synopsys IC Compiler) & PPA analysis/boost methodology *Proven capabilities in design flow development, customer’s design flow support & cross functional communication skill would be preferred. *Language: -Proficiency in English is basic requirement. Proficiency in Chinese is a plus. *Personal Attributes -Team player with good communication skills, responsibility & flexibility. -Strong skill to go into technical details to find flow solutions for customers ◆英語スキル ・ビジネスレベル

  • 転職エージェント

    株式会社A・ヒューマン

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最大手ファンダリーのMemory Design Engineer and Manager

非公開
1000万円~1199万円 / メンバー

取り扱い転職エージェント

圓山 孝一
  • 勤務地

    神奈川県

  • 仕事内容

    最大手ファンダリーのMemory Design Engineer and Manager*SRAM architecture design *Read and write critical path design and analysis *Design of key building blocks (sensing, analog, high voltage, DFT) *Chip-level design verification *Embedded non-volatile memory compiler and productization *Co-work with product/reliability engineer on silicon characterization and reliability qualification

  • 応募資格

    ◆学歴 ・大学卒以上 ◆経験・スキル *The candidates should have at least bachelor degree with 10 years of experiences, master degree with 3 years of experience or PhD degree in relevant field. *Memory experts in the field of SRAM. *Familiar with bit cell characteristics (Vmin, bit cell performance, write margin), sense amplifier design, high sigma variation analysis, race check, margin signoff. *Knowledge on high speed and low Vmin design is a plus. *English is a plus ◆英語スキル ・ビジネスレベル

  • 転職エージェント

    株式会社A・ヒューマン

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最大手ファンダリーのDesign Methodology

非公開
900万円~1099万円 / メンバー

取り扱い転職エージェント

圓山 孝一
  • 勤務地

    神奈川県

  • 仕事内容

    最大手ファンダリーのDesign Methodology/Flow Development Manager & EngineerReport To: Director or Sr. Manager Role: *Digital Design Methodology/Flow Development for TSMC advance technologies. * Responsible for design/technology performance/power/area (PPA) analysis and optimization for TSMC advance technology nodes. * EDA tools Enablement & Certification * Customer’s design flow support Responsibility: * Design/Technology PPA analysis and optimization * EDA Tool Enablement & Certification *Customer’s design flow support

  • 応募資格

    ◆学歴 ・大学卒以上 ◆経験・スキル Requirements: *Education: - M.S. degree or above in EE/CS * Minimum of 3+ years of working experience in digital design, design flow & chip implementation related field. * Familiar with APR tools (such as Cadence Innovus and Synopsys IC Compiler) & PPA analysis/boost methodology *Proven capabilities in design flow development, customer’s design flow support & cross functional communication skill would be preferred. *Language: -Proficiency in English is basic requirement. Proficiency in Chinese is a plus. *Personal Attributes -Team player with good communication skills, responsibility & flexibility. -Strong skill to go into technical details to find flow solutions for customers ◆英語スキル ・ビジネスレベル

  • 転職エージェント

    株式会社A・ヒューマン

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Senior DevOps Engineer

グローバルに展開するダイレクト系損害保険会社
1100万円~1200万円 / その他

取り扱い転職エージェント

  • 勤務地

    東京都

  • 仕事内容

    A senior DevOps engineer will support the successful development and release of technology projects by creating reliable CI/CD pipelines and automation tools as well as providing technical leadership to other engineers in the field. The senior DevOps engineer will also work in close collaboration with our Project Management Office to understand the project requirements and to translate them into technical implementations while following the organization’s guidelines and best practices. The senior DevOps engineer will also actively seek improvement opportunities in the areas of technology, cost optimization as well as simplification with a “let’s get it done” mentality. ■Key Accountabilities Design and develop CI/CD pipelines and process automation solutions. ・ Design, implement and maintain the CI/CD pipelines and the components that support it. ・ Maintain application environments with an aim towards automation. ・ Design, implement and maintain solutions to support our infrastructure

  • 応募資格

    ■Requirements (1): Technical skills, Job experiences ? Minimum of 5 years of experience in DevOps designing, implementing, and maintaining CI/CD pipelines. ? Minimum of 3 years of experience supporting orchestrated Dockerized applications (Compose, Rancher, Helm, Kubernetes, etc.) ? Minimum of 5 years of experience supporting applications on cloud platforms (AWS preferred) ? Advanced understanding about Linux, namespaces, Cgroups, SELinux, etc. ? Expertise with distributed systems from high-level diagrams all the way to processes, protocols and resources (CPU, Mem). ? Solid experience with automation and scripting (Python & Go are preferred) ? Good troubleshooting skills with Java and JavaScript based applications. ? Experience with Infrastructure and configuration as code (Terraform, Ansible, Puppet, etc.) ■Requirements (2): Behavioral skills ? Good communication skills. Able to translate technical requirements to non-technical people and vice versa. ? Be a team player who understand

  • 転職エージェント

    株式会社コトラ

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Developer (Execution Services - Equity)

大手証券会社(本社・ミドル・バック部門)
700万円~1200万円 / その他

取り扱い転職エージェント

  • 勤務地

    東京都

  • 仕事内容

    ■As a key member of the Autotrading team the candidate will ・Enhance the existing algorithm and applications supporting the algo ・Participate in the full project life cycle including technical analysis, design, data analysis and mapping, development and testing. ・Occasionally provide level 2 and 3 support for front-office applications ・Ensure adherence to functional architecture strategy and compliance to company development standards. ・Liaise with the business and development teams with regards to priorities and progress of various tasks and projects. ・If necessary, help manage projects for the implementation of new systems or system upgrades within the region.

  • 応募資格

    ■Mandatory ・Degree holder in Information Technology or equivalent ・2-3 years experience of working with software development in investment banking related environment ・Good communication skills ・Ability to exhibit high level of professionalism in team oriented environment. ・Team player that is able to work with people across different departments, countries and regions. ・Language proficiency: Fluency in English and some Japanese preferable. ・Self motivated ・Experienced in Java/C++ ■Preferred ・Good knowledge of Equities Trading platforms ・Experience in the Equity space (experience in algorithmic trading space is a plus). ・Knowledge on FIX protocol ・Good knowledge on market data platforms ・Good knowledge on GUI development is a plus ・Experience in KDB+/Q is a plus ・Experience with Solace middleware is a plus ・Good knowledge of networks, TCP/IP and enterprise messaging solutions

  • 転職エージェント

    株式会社コトラ

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Windows ドライバー 設計エンジニア

非公開
500万円~750万円 / メンバー

取り扱い転職エージェント

  • 勤務地

    東京都

  • 仕事内容

    OEM顧客向けに展開される製品に対し、Windowsプラットフォーム上で、Driverを開発、メンテナンス、イシューの解析、分析、対策などをしていただきます。 所属は、ワコムのソフトウェアアプリケーションや、ドライバーを開発し、ソフトウェアテクノロジーを牽引しているInk Divisionの所属となります。Ink DIvision自体は、ワコムのブランドビジネス、テクノロジーソリューションビジネス(OEMビジネス)両方のビジネスに関わりますが、今回はのフォーカスは、OEMビジネスとなります。 勤務地は東京ですが、上司および同僚はアメリカのポートランドオフィスにいますので、英語でのコミュニケーションは必須です。また、メインの担当顧客は中国となります。 Key Responsibilities: ・ Develop Wacom driver software for Windows platforms (Win 7, 8.1 and 10) ・ Design and implement kernel and user mode components ・ Design and implement UI components ・ Apply object-oriented design approach ・   Implement using C/C++ ・ Perform requirement analysis, design and develop accurate schedules ・ Follow department guidelines for development process, coding style, revision control ・ Test work products, developing tests if needed, before releasing to SQA ・ Work with Wacom FAE to analyze and resolve issues/bugs found in customer environment ・ May require visiting customer site on a short notice to help resolve urgent issues ・ Closely work with driver developers in Portland office

  • 応募資格

    ●30歳~45歳位迄 ・ 4+ years of SW/driver development experience on Windows ・ University degree in computer science or equivalent ・ Experience with Visual Studio ・ Solid background with C/C++ ・ Solid understanding of using Windows (device manager, service manager, registry) ・ Kernel mode driver development experience ・ Ability to work independently ・ Ability to effectively collaborate with remote colleagues and customers ・ Excellent spoken and written English Skills Requirements (Nice to have): ・ Windbg driver debugging experience ・ Knowledge of WHQL / Windows Update process ・ Good understanding on how USB HID devices work on Windows ※A few times of overseas biz trips are required in a year

  • 転職エージェント

    株式会社ジェー・エム・アール

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