転職支援にとどまらない、
メディカル人材専門のキャリア支援Platform
Medical Career Platform
メディカル業界に特化したキャリア情報を得る
キャリア支援サービスを利用する
理想のキャリアを手に入れる。
医療を変えるヒトになる。
転職支援にとどまらない、
メディカル人材専門のキャリア支援Platform
Medical Career Platform
メディカル業界に特化したキャリア情報を得る
キャリア支援サービスを利用する
メディカル業界専門のコンサルタントが対応
/メディカル業界の非公開求人多数
MCP(Medical Career Platform)で
“キャリア”全体を考えませんか?
キャリアの変化に直面したとき、
選択肢はなにも転職だけではありません
スキルアップ、異動、昇格・昇進、副業・複業、
起業、結婚、出産・育児、大学での学びなおし・・・
あなたの「ありたい姿」を見つけ、
近づくための情報や支援を得られる場所
それが「MCP」です
MCPの特徴01
コラムや辞典の執筆者、無料転職支援サービスのコンサルタント、登録キャリアカウンセラーなどは、 業界出身者などメディカルに知見のある人ばかり 質の高い情報・サポートが得られます
MCPの特徴02
求人情報、無料転職支援サービス、業界/企業/職種/用語辞典、セミナー/イベントなど
あなたの転職、キャリアアップ、スキルアップをサポートするコンテンツがたくさんあります
MCPの特徴03
会員登録いただくと、コラムや辞典の閲覧、転職支援サービス、性格検査など
閲覧、利用できるコンテンツがより充実します
※有料で提供しているサービスもございます
伝えたいことを正確に伝えるには 2 ~伝わりやすい「報告」の組み立て方~
「報告」「指示」「会議」など、コミュニケーションを取る場ごとにポイントは違います。今回はそのなかの「報告」におけるコミュニケーションのポイントをわかりやすく説明します。
「原因側に立つ」:キャリアの舵を自分で握り、未来へ進む
自身の人生を運に委ねず、自身でコントロールし、自分が欲しい結果(未来)を手にするための、心理学(NLP)に基づく持つべきマインドと考え方を紹介します。
明確に減少傾向にあるMRの状況と、今後の転職・キャリアの方向性
「このまま続けて大丈夫?」と悩み、転職する方が増えているMR。キャリアプランに悩んでいるMRへ、業界の将来性や検討可能な転職先についてご紹介します。
そのキャリアの悩み、転職エージェントへの相談で大丈夫?
キャリアに関する相談を、転職エージェントではなく、コーチや(キャリア)カウンセラー、に相談するという選択肢もあります。そのコーチングやカウンセリングについて説明します。
・国内外の薬事規制要件を理解した上で、申請資料の品質パート作成における薬事戦略を策定する。 ・社内、または製造所とコミュニケーションを取りながら、CMC薬事課題の抽出・相談・解決を行う。 ・CMC技術部門関係者と連携し、申請資料の作成を推進する。 ※ご経験に応じて、お任せする業務内容が変更する場合がございます。 ※フルタイム、パートタイムの選択可能です。
募集中
DCT Japanが持つソリューションを活用し、国内外の大手~ミドルクラスの製薬企業に対する営業職です。 製薬企業の臨床開発部門並びにメディカルアフェアーズ、CRO(国内・海外)に対して、DCTや臨床研究における当社ソリューションの活用を提案し、受注を目指していただくものです。 看護師プールがあり効率的なビジット対応が可能なこと、インテグリティ・ヘルスケアグループが持つプラットフォームやネットワークがあることが他社にない強みです。 患者の来院に依存しない臨床試験が広まることで、当社グループが目指す個別医療を実現するとともに、売上の最大化を目指します。 国内営業担当1名、海外営業担当1名、合計2名を募集します。 具体的には・・・ ・既存取引先や、ディスカッション実績がある企業、あるいはそれらの企業からの紹介、インテグリティ・ヘルスケアとの顧客連携などにより新規案件を獲得します。 ・ほとんどの商談はリモートで行います。クライアントの要望があれば対面で実施します。 ・1案件あたり数百万~1億円以上の提案で、セールスサイクルは3カ月~半年程度となります。 【働き方】 在宅中心 海外営業担当の場合、現地時間に合わせての打ち合わせがあります。
募集中
ACCOUNTABILITIES The role is accountable for the overall quality strategy and quality management system of commer-cial vaccines operations and supplies in Japan. The Head of commercial Vaccines Quality is respon-sible to design, deploy, monitor and improve the quality management system and for compliance to current Good Manufacturing/Distribution & Laboratory Practices and compliance to Takeda global standards and overall Hikari Site Standards. The Head of commercial Vaccines Quality partners with the GMS site quality head and aligns on site quality strategy, a harmonized cross-plant quality philosophy & joint quality initiatives and main-tains good day to day collaboration between the 2 site quality organizations. Ensures that new/revised quality system requirements are deployed to the site timely. Ensures execution leads for Quality-owned business processes are established who work with the business process owner to continually execute compliantly & improve on site processes. Responsible for Japan vaccine quality performance, continuous improvement and Q-metrics (KPI) monitoring to ensure global and site targets are achieved, met and countermeasures are in place when applicable. Responsible for Quality Control testing and sampling for commercial vaccines (Bulk Drug Substance and Drug Product (BDS, DP)) and partners with other Takeda laboratories or external laboratories for testing that is performed on behalf of vaccines quality (eg. Microbiology, Environmental Moni-toring, Raw Materials) Responsible to establish the appropriate quality oversight for outsourced activities such as testing as well as quality assurance review of site validation activities. Development and refinement of groups’ specific quality systems and procedures. Committed to continuous improvement and responsible to proactively mitigate current and future risks to maintain an effective operation to support business needs. Living Takeda’s values (Takeda-isms) and fostering a Quality Culture culture of trust and and speak up culture within the team. Assuring appropriate GMP and QA systems training of Quality personnel and continuously develop team´s capabilities and expertise. Accountable for quality oversight of site quality management systems (CAPAs, Change Controls, Deviations, Formal Risk Management, facility/equipment/process qualification) Responsible for site specific QMR management and gathering of APQR data. Align with GMSGQ team and provide QA support for electronic system integration: LIMS, Trackwise, SAP etc. Responsible for vaccine batch disposition decisions taking into account all relevant information and escalation processes. Oversight of execution of product disposition (drug substance). Responsible to ensure sufficient and adequate quality oversight of vaccines manufacturing and distribution processes. Preparing for/ supporting/ leading internal and health authority regulatory inspections and third-party audits, including communicating with and providing information to regulatory submissions or bodies. Responsible for timely updates of site achievements and challenges to management with a focus on quality compliance, operations performance, staff performance and productivity/training, staff development, continuous improvements, key projects support and identification and resolving obstacles to maintain a highly effective and productive functional group. Responsible for management of cross-plant quality issues and timely escalation of vaccines related issues within the global Takeda VBU organization. Responsible for budget planning and managing expenses and for timely hiring, training and devel-opment of qualified staff to ensure effective execution of roles and responsibilities, GMP compli-ance, and attainment of operational and development goals.
募集中
ACCOUNTABILITIES Develop and manage project budgets, ensuring that all expenditures are in accordance with approved budgets. Manage project risks, ensuring that risks are identified, assessed, and mitigated in a timely manner Provide regular project status updates to senior management and other stakeholders. Ensure compliance with all applicable regulations, guidelines, and policies. Provide regular management up-dates and act as an enabler for individual project teams. Use project management methodologies and skills to manage the capital project across organizational boundaries and is responsible for its successful delivery. Ensures the project is conducted at the highest quality, within time and budget, and that the risk level and stakeholder expectations are managed. Ensures adherence to the GMS GOP - Planning and Execution of Capital Investment Projects Coordinates and supervises project execution related activities, from initiation to close out and successful hand-over. Leads a cross functional team of internal and external specialists. Responsible for meeting project scope requirements, schedule requirements, and costs. Interfaces with major projects/initiatives at the specific plant. Transfers best practices across functions and business units as well as other sites. Ensures compatibility and consistency with the existing organization and industry standards (PMM, cGMP, GEP, etc.) Coordinates with all stakeholders, facilitates problem solving sessions and or other planning sessions, and makes adjustments to the project in alignment with the overall business strategy. Responsible for the adequate utilization of all quality systems as defined by Takeda Procedures within the project organization. Ensures appropriate safety measures are taken to prevent injuries and minimizes safety risks. Ensures readiness for inspections together with quality organizations. Ensures compliance with rules and regulations of procurement and accounting. DIMENSIONS AND ASPECTS Project CAPEX Size of project: about 1000 Oku Yen Technical/Functional (Line) Expertise Knowledge of manufacturing processes and engineering documents, such as facility layouts, P&IDs, equipment arrangements, facility design, and facility costs. Knowledgeable in project management methodologies (i.e.PMBOK, PMI etc.). Awareness of current state of the art in the field of pharmaceutical engineering and biotechnology and familiarity with GMP and other regulations. Knowledgeable in project controlling and scheduling Leadership Influencing and collaboration skills. Leadership and problem solving skills. Foster a culture of collaboration, continuous improvement, and innovation among project teams. Decision-making and Autonomy Within his/her area of expertise as defined at the project start. Interaction Experience working in large company environment with matrix organizations. Experience in working and communicating globally in the pharmaceutical or biotech industry. Anticipates and resolves conflict situations in a win-win outcome. Team based player. Innovation Evaluates and proposes innovative project delivery methods where applicable. Translate innovation initiatives across Takeda into project execution and design. Complexity Must be self-motivated, have good interpersonal skills, capable of analyzing and solving complex problems through innovative thought and experience.
募集中
職務内容 以下のワクチン注射製剤の製剤開発に関する業務に従事頂きます。 製剤設計(処方、剤形の設計) 製剤製造プロセス設計(治験段階~商用に応じた製剤製造法の開発) バリデーション、治験薬製造設備・機器の管理、治験薬製造・供給 商用スケールへのスケールアップ検討、商用部門への引き継ぎ 申請書類の作成、照会事項対応、査察対応など
募集中
Microsoft 365 Administration: Ensure data integrity and security by evaluating, implementing, and managing appropriate Microsoft 365 hardware and software solutions utilizing industry standards and best practices. Manage Microsoft 365 licenses, subscriptions, and users across the organization. Provide technical support to end-users to resolve any issues and/or fulfill user's requirement related to Microsoft 365 services. Interact with end-users directly to capture the user's demand via multiple communication channels, including face-to-face, remote session, and email/chat . Deploy Microsoft 365 software installations, configurations, and upgrades across a diverse customer base. Ensure compliance with established standards, policies, best practices, and configuration guidelines. Develop and document standards and procedures for Microsoft 365 administration and maintenance. ITSM Incident, Request, and Change Management: Manage and respond to Microsoft 365 incidents and service requests using IT Service Management (ITSM) tools and processes. Collaborate with the ITSM team to plan/test Microsoft 365 related changes to minimize business disruptions complying with the standard change management policies. Develop and maintain Microsoft 365 service processes and documents for incident, request, and change management. Ensure timely resolution of Microsoft 365 incidents and service requests to meet the expected service level and minimize impact on end-users.
募集中
Responsibilities include: Manage day to day Chief of Staff Office responsibilities ensuring a smooth operation and coordination in GCA Lead as a point of contact for GCA members and other stakeholders, representing the Chief of Staff Office and directly supporting the Chief Global Corporate Affairs and Sustainability Officer Work with GCA Leadership Team (GCALT) and Finance Business Partner to monitor and track the budget spending vs plan Lead GCA-wide strategic initiatives and employee engagement activities, including facilitation, troubleshooting stakeholder management and decision making Contribute to key GCA priorities including corporate communications, sustainabilty, and public affairs Lead preparation and facilitation of the GCA monthly meetings and Townhalls Lead Chief Global Corporate Affairs and Sustainability Officer’s presentation development and coordination Support Chief of Staff and Head of Global CSR and Partnership Strategy with additional tasks as needed
募集中
Accountabilities: Develops project or significant technical strategy and leverages technical skill(s) as a resource/expert within the department Contributes significantly and independently to project work which may include multiple projects within functional area. Plans and implements resolutions to technical problems/issues Independently designs and executes experiments, and reports results Recommends, justifies and implements technologies and innovations. Owns a discipline/technical skill in its entirety and continues to develop expertise in other key technical skills. Influences and supports initiatives related to driving scientific and technical improvement within function and potentially cross-functionally. Reviews, interprets and communicates data cross functionally within pharmaceutical sciences and project teams Conducts analysis of technical and conceptual risk and trends Identifies process trends and defines/champions process strategy or use of novel technologies Recognized as a technical expert and resource within function Significant technical responsibility for a project area/technical program within the department and potentially across Pharmaceutical sciences Identifies topics for initiatives and leads local/global initiatives on behalf of senior staff. Defines appropriately complex/novel approaches and methodologies to solving outstanding technical challenges Coordinates and leads technology transfer to internal or external manufacturing sites Responsible for authoring relevant sections of regulatory documents, validation plans, reports and peer reviewed manuscripts. Proactively identifies vendors and builds relationships to gain access to technologies as needed to deliver on pipeline goals. Manages key vendor relationships across multiple projects as appropriate, and proactively affects resolution of issues arising at vendors. Represents Takeda and is an active member on pre-competitive collaborations with academic and industrial partners. Education and Experience: A Ph.D. degree with 3+ years of academic, post-doctoral or pharmaceutical industry experience; an MS degree with 9+ years of pharmaceutical industry experience; or a BS degree with 11+ years of pharmaceutical industry experience. Degrees in chemical engineering required. Experience in the use of mathematical, both statistical and first principle, models as well as advanced process control systems preferred Experience in building reaction kinetic models as well as process models preferred. Experience in building laboratory and pilot plant equipment a plus Experience in crystallization process development and scale-up with an emphasis on form, purity, and particle size control a plus Experience in the use and scale-up of milling technologies (both dry and wet) for particle size control a plus Experience in the use of process analytical technologies (FT-IR, NIR, FBRM, UV-vis, etc.) required Experience in building chemometric models preferred Experience in developing continuous processes a plus Sound knowledge of current Good Manufacturing Practices (cGMP) preferred Experience working in a pilot plant a plus Previous experience with the use of contract facilities and managing technical transfers a plus Experience in working in a multi-disciplinary team environment Proven scientific track record through presentations at scientific conferences and publication of pier reviewed manuscripts
募集中