Job About the role • The VP Head of Global Product Strategy for Neuroscience is a strategic leadership position that is accountable for the development and execution of strategies for the Neuroscience business and each of the associated last liter products.
Job About the role • The VP Head of Global Product Strategy for Neuroscience is a strategic leadership position that is accountable for the development and execution of strategies for the Neuroscience business and each of the associated last liter products.
Join us as an Associate Medical Director, Clinical Science, GI2 TAU in our Cambridge, MA office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company.
Join us as an Associate Medical Director, Clinical Science, GI2 TAU in our Cambridge, MA office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company.
This role is within the Global Regulatory Affairs (GRA) Chemistry Manufacturing & Controls (CMC) and Devices organization, and will contribute to the team’s delivery of critical functions as follows: Independently develops the regulatory CMC strategy and leads the execution of regulatory CMC investigational, registration and post-approval strategies for their assigned product(s) as the GRA CMC Product • Lead.
This role is within the Global Regulatory Affairs (GRA) Chemistry Manufacturing & Controls (CMC) and Devices organization, and will contribute to the team’s delivery of critical functions as follows: Independently develops the regulatory CMC strategy and leads the execution of regulatory CMC investigational, registration and post-approval strategies for their assigned product(s) as the GRA CMC Product • Lead.
This role is within the Global Regulatory Affairs (GRA) Chemistry Manufacturing & Controls (CMC) and Devices organization, and will contribute to the team’s delivery of critical functions as follows: Independently develops the regulatory CMC strategy and leads the execution of regulatory CMC investigational, registration and post-approval strategies for their assigned product(s) and may serve as the GRA CMC Product • Lead, as required.
This role is within the Global Regulatory Affairs (GRA) Chemistry Manufacturing & Controls (CMC) and Devices organization, and will contribute to the team’s delivery of critical functions as follows: Independently develops the regulatory CMC strategy and leads the execution of regulatory CMC investigational, registration and post-approval strategies for their assigned product(s) and may serve as the GRA CMC Product • Lead, as required.
Join us as an Associate Medical Director in our Neuroscience Therapeutic Area Unit in our Cambridge, MA office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company.
Join us as an Associate Medical Director in our Neuroscience Therapeutic Area Unit in our Cambridge, MA office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company.
Assesses scientific, medical, and development feasibility, evaluating strategic fit with overall portfolio, evaluating complete or ongoing clinical trials, assessing regulatory interactions and future development plans., interacting with upper management of potential partner/acquisition companies during DD visits and alliance negotiations, and representing clinical science on internal assessment teams.
Assesses scientific, medical, and development feasibility, evaluating strategic fit with overall portfolio, evaluating complete or ongoing clinical trials, assessing regulatory interactions and future development plans., interacting with upper management of potential partner/acquisition companies during DD visits and alliance negotiations, and representing clinical science on internal assessment teams.
Join us as a Medical Director, Clinical Science, Neuroscience- Psychiatry in our Cambridge, MA office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company.
Join us as a Medical Director, Clinical Science, Neuroscience- Psychiatry in our Cambridge, MA office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company.
Join us as a Medical Director, Clinical Science, Neuroscience TAU- Sleep Medicine in our Cambridge, MA office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company.
Join us as a Medical Director, Clinical Science, Neuroscience TAU- Sleep Medicine in our Cambridge, MA office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company.
POSITION OBJECTIVES The Medical Director leads and drives strategy for the overall global (US/EU/Japan) clinical development taking into consideration the medical, scientific, regulatory and commercial issues for assigned Takeda pipeline compounds. • Leads a multi-disciplinary, multi-regional, matrix team through highly complex decisions.
POSITION OBJECTIVES The Medical Director leads and drives strategy for the overall global (US/EU/Japan) clinical development taking into consideration the medical, scientific, regulatory and commercial issues for assigned Takeda pipeline compounds. • Leads a multi-disciplinary, multi-regional, matrix team through highly complex decisions.
POSITION OBJECTIVES The Medical Director leads and drives strategy for the overall global (US/EU/Japan) clinical development taking into consideration the medical, scientific, regulatory and commercial issues for assigned Takeda pipeline compounds. • Leads a multi-disciplinary, multi-regional, matrix team through highly complex decisions.
POSITION OBJECTIVES The Medical Director leads and drives strategy for the overall global (US/EU/Japan) clinical development taking into consideration the medical, scientific, regulatory and commercial issues for assigned Takeda pipeline compounds. • Leads a multi-disciplinary, multi-regional, matrix team through highly complex decisions.
POSITION OBJECTIVES The Associate Director, Drug–Device Combination Development • Lead (DDL) is responsible for leading and coordinating drug–device combination product development activities for assigned assets across the product lifecycle.
$154,400 - $242,550
On-site
EDUCATION, BEHAVIORAL COMPETENCIES AND SKILLS:
Education and Experience Requirements
BS/BEng in engineering, pharmaceutical sciences, materials science, or related discipline required
POSITION OBJECTIVES The Associate Director, Drug–Device Combination Development • Lead (DDL) is responsible for leading and coordinating drug–device combination product development activities for assigned assets across the product lifecycle.
$154,400 - $242,550
On-site
EDUCATION, BEHAVIORAL COMPETENCIES AND SKILLS:
Education and Experience Requirements
BS/BEng in engineering, pharmaceutical sciences, materials science, or related discipline required
How you will contribute Execute and monitor experiments using cell culture and upstream unit operations (bench-top bioreactors, Ambr, shake flasks, WAVE bioreactors, high-throughput purification systems) Operate and monitor bioprocess equipment using DeltaV or similar process control systems Maintain laboratory equipment and ensure day-to-day operational readiness • Partner with senior engineers to plan and execute larger studies and experiments Document experimental work in electronic laboratory notebooks with clear, accurate, and timely records Perform basic data analysis to evaluate trends and support study conclusions Prepare technical summaries and study updates to communicate findings Adhere to laboratory procedures, quality standards, and safety requirements • Support continuous improvement efforts related to workflows, data capture, and execution • Contribute to project tasks and small initiatives under guidance What you bring to Takeda Associate’s degree with 2+ years of relevant experience, or Bachelor’s degree in chemical engineering, biological engineering, biotechnology, biology, or a related field, with relevant laboratory or process development experience • Experience in cell culture, upstream process development, or biotherapeutics development • Hands-on experience with bioreactors, shake flasks, or related upstream platforms • Familiarity with DeltaV or similar process control systems • Experience using electronic laboratory notebooks for documentation Ability to perform basic data analysis and clearly communicate findings • Strong technical writing skills for reports and documentation Understanding of laboratory practices, development processes, and quality requirements • Strong attention to detail with the ability to follow procedures and maintain accurate records Ability to work effectively under guidance in a collaborative team environment More about us At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs.
How you will contribute Execute and monitor experiments using cell culture and upstream unit operations (bench-top bioreactors, Ambr, shake flasks, WAVE bioreactors, high-throughput purification systems) Operate and monitor bioprocess equipment using DeltaV or similar process control systems Maintain laboratory equipment and ensure day-to-day operational readiness • Partner with senior engineers to plan and execute larger studies and experiments Document experimental work in electronic laboratory notebooks with clear, accurate, and timely records Perform basic data analysis to evaluate trends and support study conclusions Prepare technical summaries and study updates to communicate findings Adhere to laboratory procedures, quality standards, and safety requirements • Support continuous improvement efforts related to workflows, data capture, and execution • Contribute to project tasks and small initiatives under guidance What you bring to Takeda Associate’s degree with 2+ years of relevant experience, or Bachelor’s degree in chemical engineering, biological engineering, biotechnology, biology, or a related field, with relevant laboratory or process development experience • Experience in cell culture, upstream process development, or biotherapeutics development • Hands-on experience with bioreactors, shake flasks, or related upstream platforms • Familiarity with DeltaV or similar process control systems • Experience using electronic laboratory notebooks for documentation Ability to perform basic data analysis and clearly communicate findings • Strong technical writing skills for reports and documentation Understanding of laboratory practices, development processes, and quality requirements • Strong attention to detail with the ability to follow procedures and maintain accurate records Ability to work effectively under guidance in a collaborative team environment More about us At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs.
How you will contribute • Support the design and execution of upstream development studies across early- and late-stage programs • Collaborate with upstream, downstream, and analytical teams as part of cross-functional development efforts Operate and troubleshoot cell culture systems, including bench-top bioreactors, Ambr, shake flasks, WAVE bioreactors, and high-throughput purification systems Utilize DeltaV or similar control systems to support process execution and data collection Maintain accurate and timely documentation in electronic laboratory notebooks Analyze process data, interpret results, and summarize findings to support development decisions Prepare technical reports, study summaries, and supporting documentation Learn and apply artificial intelligence and in silico tools to enhance process understanding and efficiency What you bring to Takeda Bachelor’s degree with 5+ years, or Master’s degree with 3+ years of relevant experience in biochemical engineering, chemical engineering, biotechnology, biology, or related field • Experience in biotherapeutics upstream process development • Hands-on experience with upstream unit operations, including bioreactors (bench-top and Ambr), shake flasks, and WAVE systems Working knowledge of DeltaV or similar process control systems • Experience using electronic laboratory notebooks • Strong data analysis and technical writing skills Solid understanding of upstream cell culture process development Ability to learn and apply new tools and technologies, including AI and in silico methods • Strong attention to detail with the ability to work independently and collaboratively • Proven ability to contribute to team objectives and support broader project goals More about us At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs.
How you will contribute • Support the design and execution of upstream development studies across early- and late-stage programs • Collaborate with upstream, downstream, and analytical teams as part of cross-functional development efforts Operate and troubleshoot cell culture systems, including bench-top bioreactors, Ambr, shake flasks, WAVE bioreactors, and high-throughput purification systems Utilize DeltaV or similar control systems to support process execution and data collection Maintain accurate and timely documentation in electronic laboratory notebooks Analyze process data, interpret results, and summarize findings to support development decisions Prepare technical reports, study summaries, and supporting documentation Learn and apply artificial intelligence and in silico tools to enhance process understanding and efficiency What you bring to Takeda Bachelor’s degree with 5+ years, or Master’s degree with 3+ years of relevant experience in biochemical engineering, chemical engineering, biotechnology, biology, or related field • Experience in biotherapeutics upstream process development • Hands-on experience with upstream unit operations, including bioreactors (bench-top and Ambr), shake flasks, and WAVE systems Working knowledge of DeltaV or similar process control systems • Experience using electronic laboratory notebooks • Strong data analysis and technical writing skills Solid understanding of upstream cell culture process development Ability to learn and apply new tools and technologies, including AI and in silico methods • Strong attention to detail with the ability to work independently and collaboratively • Proven ability to contribute to team objectives and support broader project goals More about us At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs.
Job About the role • The Staff Engineer, Upstream Process Development is responsible for developing, characterizing, and defining cell culture processes across multiple modes, including fed-batch, perfusion, and intensified fed-batch systems.
$116,000 - $182,270
On-site
in upstream operations and process development strategies.
How you will contribute
Develop, characterize, and optimize cell culture processes across fed-batch, perfusion, and intensified fed-batch platforms
Job About the role • The Staff Engineer, Upstream Process Development is responsible for developing, characterizing, and defining cell culture processes across multiple modes, including fed-batch, perfusion, and intensified fed-batch systems.
$116,000 - $182,270
On-site
in upstream operations and process development strategies.
How you will contribute
Develop, characterize, and optimize cell culture processes across fed-batch, perfusion, and intensified fed-batch platforms
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 Director, Research Strategy Development POSITION Takeda Development Center Americas, Inc. is seeking a Director, Research Strategy Development with the following duties • partner with Research Senior Leadership to define, prioritize, and execute enterprise-level research strategy initiatives aligned with long-term scientific and business objectives. • Design and apply quantitative research strategy and portfolio decision-making frameworks to evaluate the impact of portfolio and operating model decisions on resourcing, budget, and execution scenarios. • Support Research Senior Leadership, in collaboration with Finance and other enabling functions, in translating research strategy into financial plans, budgets, and resource allocation decisions. • Develop and structure strategic communications, narratives, and materials to support research investment proposals, budget requests, and business cases presented to executive leadership and the C-suite. • Support senior Research Leadership in communicating research strategy, portfolio decisions, and investment rationale to enterprise-level stakeholders, including executive leadership. • Lead and support organizational and operating model transformation initiatives within Research to improve decision-making, governance, and execution effectiveness. • Collaborate with cross-functional teams to define research priorities, align resources, and ensure timely execution of strategic initiatives.
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 Director, Research Strategy Development POSITION Takeda Development Center Americas, Inc. is seeking a Director, Research Strategy Development with the following duties • partner with Research Senior Leadership to define, prioritize, and execute enterprise-level research strategy initiatives aligned with long-term scientific and business objectives. • Design and apply quantitative research strategy and portfolio decision-making frameworks to evaluate the impact of portfolio and operating model decisions on resourcing, budget, and execution scenarios. • Support Research Senior Leadership, in collaboration with Finance and other enabling functions, in translating research strategy into financial plans, budgets, and resource allocation decisions. • Develop and structure strategic communications, narratives, and materials to support research investment proposals, budget requests, and business cases presented to executive leadership and the C-suite. • Support senior Research Leadership in communicating research strategy, portfolio decisions, and investment rationale to enterprise-level stakeholders, including executive leadership. • Lead and support organizational and operating model transformation initiatives within Research to improve decision-making, governance, and execution effectiveness. • Collaborate with cross-functional teams to define research priorities, align resources, and ensure timely execution of strategic initiatives.
Job About the role • The Staff Engineer, Downstream Process Development is responsible for developing, characterizing, and defining purification processes for biotherapeutics.
$116,000 - $182,270
On-site
in downstream operations such as chromatography, harvest, ultrafiltration/diafiltration (UF/DF), and viral clearance, with potential exposure to bioconjugation.
How you will contribute
Develop, characterize, and optimize purification processes for biotherapeutics
Job About the role • The Staff Engineer, Downstream Process Development is responsible for developing, characterizing, and defining purification processes for biotherapeutics.
$116,000 - $182,270
On-site
in downstream operations such as chromatography, harvest, ultrafiltration/diafiltration (UF/DF), and viral clearance, with potential exposure to bioconjugation.
How you will contribute
Develop, characterize, and optimize purification processes for biotherapeutics
OBJECTIVES The Medical Director leads and drives strategy for the overall global (US/EU/Japan) clinical development taking into consideration the medical, scientific, regulatory and commercial issues for assigned Takeda pipeline compounds. • Leads a multi-disciplinary, multi-regional, matrix team through highly complex decisions.
OBJECTIVES The Medical Director leads and drives strategy for the overall global (US/EU/Japan) clinical development taking into consideration the medical, scientific, regulatory and commercial issues for assigned Takeda pipeline compounds. • Leads a multi-disciplinary, multi-regional, matrix team through highly complex decisions.
Job • Senior Director, AIRx Discovery Biology • Lead Takeda Research is constructing the Discovery Automation & Robotics (DAR) group built on AI, automation, new ways of working, and talent with the singular vision of delivering differentiated medicines to the clinic at speed and cost.
Job • Senior Director, AIRx Discovery Biology • Lead Takeda Research is constructing the Discovery Automation & Robotics (DAR) group built on AI, automation, new ways of working, and talent with the singular vision of delivering differentiated medicines to the clinic at speed and cost.
Job About the role • Join Takeda as a Manager, Decision Science Center of Excellence where you lead brand-level promotional mix modeling and campaign lift assessment within the Decision Science team.
Job About the role • Join Takeda as a Manager, Decision Science Center of Excellence where you lead brand-level promotional mix modeling and campaign lift assessment within the Decision Science team.