Job • Join Takeda as a Director, Predictive Analytics and AI out of our Cambridge, MA office. We are seeking a visionary Director to lead our Data Science team, transforming pharmaceutical commercialization with advanced data science and AI.
$177,000 - $278,080
On-site
business acumen, and creative strategy to translate sophisticated analytics into actionable business solutions, delivering commercial excellence in areas such as trialist identification, patient segmentation, next-best-action (NBA), target prioritization dynamic targeting, and execution of AI/ML strategies to enable scalable personalization across HCP and patient stakeholders.
The leader brings a consultative approach to partnering with stakeholders to identify new business opportunities, develop advanced analytic insights informing strategies, and drive AI/ML & data driven decision making for business growth. You will collaborate with internal and external stakeholders to ensure models can be deployed in compliant, production-ready environments with clear plans to measure effectiveness.
Job • Join Takeda as a Director, Predictive Analytics and AI out of our Cambridge, MA office. We are seeking a visionary Director to lead our Data Science team, transforming pharmaceutical commercialization with advanced data science and AI.
$177,000 - $278,080
On-site
business acumen, and creative strategy to translate sophisticated analytics into actionable business solutions, delivering commercial excellence in areas such as trialist identification, patient segmentation, next-best-action (NBA), target prioritization dynamic targeting, and execution of AI/ML strategies to enable scalable personalization across HCP and patient stakeholders.
The leader brings a consultative approach to partnering with stakeholders to identify new business opportunities, develop advanced analytic insights informing strategies, and drive AI/ML & data driven decision making for business growth. You will collaborate with internal and external stakeholders to ensure models can be deployed in compliant, production-ready environments with clear plans to measure effectiveness.
Job About the role • The Utilities Supervisor is responsible for implementing, supervising daily operation and maintenance activities of utilities equipment at the site.
Job About the role • The Utilities Supervisor is responsible for implementing, supervising daily operation and maintenance activities of utilities equipment at the site.
Job About the role • The Utilities Supervisor is responsible for implementing, supervising daily operation and maintenance activities of utilities equipment at the site.
Job About the role • The Utilities Supervisor is responsible for implementing, supervising daily operation and maintenance activities of utilities equipment at the site.
What you bring to Takeda BS engineering with a minimum of 10+ years’ experience in validation. • Experience with systems like LIMS, MES, ERP, SCADA, or DCS (e.g., Delta V) for computer systems validation engineers is desirable.
$116,000 - $182,270
On-site
to define validation approaches and execution of system validation activities in accordance with cGMP and applicable regulations, procedures, and industry guidance.
Basic understanding of data and statistical analysis of validation test results.
Knowledge of cGMPs or equivalent regulations, validation associated regulations, guidelines, and best practices.
What you bring to Takeda BS engineering with a minimum of 10+ years’ experience in validation. • Experience with systems like LIMS, MES, ERP, SCADA, or DCS (e.g., Delta V) for computer systems validation engineers is desirable.
$116,000 - $182,270
On-site
to define validation approaches and execution of system validation activities in accordance with cGMP and applicable regulations, procedures, and industry guidance.
Basic understanding of data and statistical analysis of validation test results.
Knowledge of cGMPs or equivalent regulations, validation associated regulations, guidelines, and best practices.
Objective / Purpose The Director, High-Throughput In Vitro ADME is a senior scientific and operational leader responsible for building and directing Takeda’s high-throughput in vitro ADME capabilities in support of small- and large-molecule discovery programs.
Objective / Purpose The Director, High-Throughput In Vitro ADME is a senior scientific and operational leader responsible for building and directing Takeda’s high-throughput in vitro ADME capabilities in support of small- and large-molecule discovery programs.
The Senior Project Management • Lead champions Takeda’s Project Management Methodology (PMM) and PMO processes, applying strong project leadership and management capabilities to oversee projects of varying scope, scale, and complexity.
The Senior Project Management • Lead champions Takeda’s Project Management Methodology (PMM) and PMO processes, applying strong project leadership and management capabilities to oversee projects of varying scope, scale, and complexity.
As Executive Director, Global Regulatory Affairs CMC Devices and Drug-Device Combination Product, you will provide strategic leadership and development to global regulatory subject matter experts to ensure innovative and robust regulatory strategies for medical devices and drug-device combination products, maximizing global regulatory success and minimizing time to approval/clearance. • Establish best practices and builds a strong regulatory community across Global Regulatory Affairs spanning device, combination product, quality, clinical, development and manufacturing interfaces.
As Executive Director, Global Regulatory Affairs CMC Devices and Drug-Device Combination Product, you will provide strategic leadership and development to global regulatory subject matter experts to ensure innovative and robust regulatory strategies for medical devices and drug-device combination products, maximizing global regulatory success and minimizing time to approval/clearance. • Establish best practices and builds a strong regulatory community across Global Regulatory Affairs spanning device, combination product, quality, clinical, development and manufacturing interfaces.
We are looking for a leader who is highly collaborative and results-oriented to support a specific product launch and champion our Global Launch Excellence community.
We are looking for a leader who is highly collaborative and results-oriented to support a specific product launch and champion our Global Launch Excellence community.
Job • Global Category Manager CRO(Contract Research Organizations) The Global Category Management for Contract Research Organizations (CRO) is responsible for leading the strategic sourcing and procurement activities for all CRO services with greater than 600 Million USD annual spend, required for Clinical Development across Takeda.
Job • Global Category Manager CRO(Contract Research Organizations) The Global Category Management for Contract Research Organizations (CRO) is responsible for leading the strategic sourcing and procurement activities for all CRO services with greater than 600 Million USD annual spend, required for Clinical Development across Takeda.
Job About the role • Join our team as a Senior Operational Excellence Specialist, where you’ll connect and collaborate across global and regional networks to bring leading Good Practices to our site—and share our site’s Good Practices with others.
Job About the role • Join our team as a Senior Operational Excellence Specialist, where you’ll connect and collaborate across global and regional networks to bring leading Good Practices to our site—and share our site’s Good Practices with others.
Job About the Role • Reporting to the Head Counsel, Global Data, Digital & Technology, the • Lead Counsel, Data, Digital & Technology serves as a senior director–level strategic legal advisor and trusted business partner to Takeda’s Global Data, Digital & Technology (GDD&T) function and related enterprise stakeholders.
Job About the Role • Reporting to the Head Counsel, Global Data, Digital & Technology, the • Lead Counsel, Data, Digital & Technology serves as a senior director–level strategic legal advisor and trusted business partner to Takeda’s Global Data, Digital & Technology (GDD&T) function and related enterprise stakeholders.
Job Title Product Owner, Tetrascience Data Platform Location: Cambridge, MA About the role As the Product Owner, Tetrascience Data Platform , you will shape the future of our Tetrascience Data Platform and SAIL Partnership on our Research, PharmSci, and PDT R&D Data, Digital and Technology team.
Job Title Product Owner, Tetrascience Data Platform Location: Cambridge, MA About the role As the Product Owner, Tetrascience Data Platform , you will shape the future of our Tetrascience Data Platform and SAIL Partnership on our Research, PharmSci, and PDT R&D Data, Digital and Technology team.
You will be entitled to Help ensure training content is properly managed and housed in appropriate repositories and support the timely execution of key medical content tactics and activities. • Support the agile development, execution, and continuous refinement of external-facing medical content that is compliant and scientifically rigorous. • Support the design and development of scientific and disease/product content in alignment with Takeda’s Business Rules and aligned processes. • Collaborate with subject matter experts to develop content that accurately reflects scientific data and aligns with Medical objectives and strategy.
You will be entitled to Help ensure training content is properly managed and housed in appropriate repositories and support the timely execution of key medical content tactics and activities. • Support the agile development, execution, and continuous refinement of external-facing medical content that is compliant and scientifically rigorous. • Support the design and development of scientific and disease/product content in alignment with Takeda’s Business Rules and aligned processes. • Collaborate with subject matter experts to develop content that accurately reflects scientific data and aligns with Medical objectives and strategy.
656.10, you are hereby notified that an application for Alien Employment Certification will be filed by Takeda Development Center Americas, Inc. for the following job opportunity: JOB LOCATION Cambridge, MA POSITION Head, R&D Automation Platform POSITION Takeda Development Center Americas, Inc. is seeking a Head, R&D Automation Platform with the following duties lead the Research and Development data automation efforts to support Takeda R&D's vision to create a development engine and ecosystem that provides optimal clinical data control and quality in a predictable, automated & cost-effective way; in collaboration with the system and architecture team, drive decisions on end-to-end systems selection & implementation, process improvement and data standards opportunities to ensure and optimize the use of automation and AI/ML; show influential strategic, execution and delivery leadership both within Takeda and outside of Takeda with vendors and partners; oversee in-house built, deployment and maintenance of automated tools, scripts, and programs to increase management speed and quality of clinical trial data; provide strategic vision for long-term delivery innovation; partners with relevant stakeholders within the global data program to define priority use cases and set up execution plan; develop test & deploy timeline for top priority use cases; define & develop Proof of Concept approach for top priority use cases; select vendors (when available), develop & test prototypes; create operationalization & roll-out roadmap for prototyped use cases, including key activities, milestones, requirements for handing off integration to adjacent functions; supports executive leadership to achieve the vision and direction for the global data program; reports on progress of projects, issues/plans, and critical path schedules to executive leadership; visibly engages across the organization to ensure transformational impact; up to 25% domestic travel to meet stakeholders for R&D Engagement week; up to 75% remote work allowed.
656.10, you are hereby notified that an application for Alien Employment Certification will be filed by Takeda Development Center Americas, Inc. for the following job opportunity: JOB LOCATION Cambridge, MA POSITION Head, R&D Automation Platform POSITION Takeda Development Center Americas, Inc. is seeking a Head, R&D Automation Platform with the following duties lead the Research and Development data automation efforts to support Takeda R&D's vision to create a development engine and ecosystem that provides optimal clinical data control and quality in a predictable, automated & cost-effective way; in collaboration with the system and architecture team, drive decisions on end-to-end systems selection & implementation, process improvement and data standards opportunities to ensure and optimize the use of automation and AI/ML; show influential strategic, execution and delivery leadership both within Takeda and outside of Takeda with vendors and partners; oversee in-house built, deployment and maintenance of automated tools, scripts, and programs to increase management speed and quality of clinical trial data; provide strategic vision for long-term delivery innovation; partners with relevant stakeholders within the global data program to define priority use cases and set up execution plan; develop test & deploy timeline for top priority use cases; define & develop Proof of Concept approach for top priority use cases; select vendors (when available), develop & test prototypes; create operationalization & roll-out roadmap for prototyped use cases, including key activities, milestones, requirements for handing off integration to adjacent functions; supports executive leadership to achieve the vision and direction for the global data program; reports on progress of projects, issues/plans, and critical path schedules to executive leadership; visibly engages across the organization to ensure transformational impact; up to 25% domestic travel to meet stakeholders for R&D Engagement week; up to 75% remote work allowed.
656.10, you are hereby notified that an application for Alien Employment Certification will be filed by Baxalta US, Inc. for the following job opportunity: JOB LOCATION Social Circle, GA POSITION Automation – EBM Manager POSITION Baxalta US Inc. is seeking a Automation – EBM Manager with the following duties • Manage and coordinate the EBM team, initiative and project; Make suggestions on improvements based on supporting data, technical knowledge, engineering principles and current industry practices; • Manage or support EBM activities for capital project with minimal assistance; • Lead the planning and execution of EBM automation activities for operational activities and capital projects by working in cross-functional teams as the Engineering lead for the EBM automation area; • Define project scopes, prepare time or cost estimates, and provide justification for operational initiative and capital budget; • Manage and control spending of approved operational and capital automation project funds; • Drive projects to completion, timeline, budget objectives; • Create or update technical support specifications (Design/Functional/System) related to project assignments; Supervise contractors and junior level engineering personnel on project and operational support activities; Demonstrate continuous improvement with respect to increasing job knowledge and proficiency related to engineering in the biopharmaceutical industry, as well as technical understanding and problem-solving capability; Stay informed with biopharmaceutical industry best practices and technologies; • Evaluate customer problems or requirements and address those through the system solutions or design; • Design and implement changes to EBM or automation systems while adhering to pharmaceutical validation and change control systems problems; Perform event’s investigation related to EBM automation system and implement the corrective and preventative action required to address the event; Perform and document hardware/software modifications, and system functional specification updates; Prepare standard operating procedures for new and existing control equipment; • Mentor Automation Engineers EBM.
656.10, you are hereby notified that an application for Alien Employment Certification will be filed by Baxalta US, Inc. for the following job opportunity: JOB LOCATION Social Circle, GA POSITION Automation – EBM Manager POSITION Baxalta US Inc. is seeking a Automation – EBM Manager with the following duties • Manage and coordinate the EBM team, initiative and project; Make suggestions on improvements based on supporting data, technical knowledge, engineering principles and current industry practices; • Manage or support EBM activities for capital project with minimal assistance; • Lead the planning and execution of EBM automation activities for operational activities and capital projects by working in cross-functional teams as the Engineering lead for the EBM automation area; • Define project scopes, prepare time or cost estimates, and provide justification for operational initiative and capital budget; • Manage and control spending of approved operational and capital automation project funds; • Drive projects to completion, timeline, budget objectives; • Create or update technical support specifications (Design/Functional/System) related to project assignments; Supervise contractors and junior level engineering personnel on project and operational support activities; Demonstrate continuous improvement with respect to increasing job knowledge and proficiency related to engineering in the biopharmaceutical industry, as well as technical understanding and problem-solving capability; Stay informed with biopharmaceutical industry best practices and technologies; • Evaluate customer problems or requirements and address those through the system solutions or design; • Design and implement changes to EBM or automation systems while adhering to pharmaceutical validation and change control systems problems; Perform event’s investigation related to EBM automation system and implement the corrective and preventative action required to address the event; Perform and document hardware/software modifications, and system functional specification updates; Prepare standard operating procedures for new and existing control equipment; • Mentor Automation Engineers EBM.
The Head of Automated Small Molecule Synthesis leads the strategy, design, and execution of small molecule synthesis using fully automated, robotic platforms to accelerate decision-making across Takeda’s discovery portfolio by quickly and reliably generating compound sets for testing.
The Head of Automated Small Molecule Synthesis leads the strategy, design, and execution of small molecule synthesis using fully automated, robotic platforms to accelerate decision-making across Takeda’s discovery portfolio by quickly and reliably generating compound sets for testing.
Oversee forecast planning and inventory management of all relevant investigational medicines and comparators for portfolio, leading in matrix of SMEs spanning Takeda supply chain, Takeda pharmaceutical sciences organizations and external partners. • Lead operational feasibility assessment, scenario analysis and risk mitigation for new clinical protocols, representing the clinical supply chain to global PS teams and global program teams. • Develop and maintain detailed clinical supply models for supply scenarios which provides a study baseline against which to monitor assumptions and inventories of finished goods in ongoing clinical trials. • Lead establishment of enterprise approach to supply/demand modelling, risk identification, and scenario planning for clinical supply chain, lead cross functional planning teams to respond to unplanned events. • Develop supply options, facilitate decision making, and communicate updated manufacturing and supply plans to all impacted stakeholders. • Responsible for execution of Operational Supply Plan throughout development lifecycle, identifying leading indicators of supply risk and escalating through PS • Lead and GPL to course correct.
Oversee forecast planning and inventory management of all relevant investigational medicines and comparators for portfolio, leading in matrix of SMEs spanning Takeda supply chain, Takeda pharmaceutical sciences organizations and external partners. • Lead operational feasibility assessment, scenario analysis and risk mitigation for new clinical protocols, representing the clinical supply chain to global PS teams and global program teams. • Develop and maintain detailed clinical supply models for supply scenarios which provides a study baseline against which to monitor assumptions and inventories of finished goods in ongoing clinical trials. • Lead establishment of enterprise approach to supply/demand modelling, risk identification, and scenario planning for clinical supply chain, lead cross functional planning teams to respond to unplanned events. • Develop supply options, facilitate decision making, and communicate updated manufacturing and supply plans to all impacted stakeholders. • Responsible for execution of Operational Supply Plan throughout development lifecycle, identifying leading indicators of supply risk and escalating through PS • Lead and GPL to course correct.
Job Title Technical Business Partner, Large Molecule Capabilities Location: Cambridge, MA (Hybrid) About the role As the Director, Technology Business Partner for Large Molecule Capabilities, you will hold a leadership role in supporting the R&D digital transformation.
Job Title Technical Business Partner, Large Molecule Capabilities Location: Cambridge, MA (Hybrid) About the role As the Director, Technology Business Partner for Large Molecule Capabilities, you will hold a leadership role in supporting the R&D digital transformation.
Leveraging advanced automation systems and statistical analysis, this individual will ensure high-throughput, reproducible, and high-quality data generation to support iterative AI-integrated Design–Make–Test–Analyze (DMTA) cycles for both small- and large-molecule discovery.
Leveraging advanced automation systems and statistical analysis, this individual will ensure high-throughput, reproducible, and high-quality data generation to support iterative AI-integrated Design–Make–Test–Analyze (DMTA) cycles for both small- and large-molecule discovery.