Director, Regulatory Capability Development and Knowledge Management
Takeda
Summary
The Director, Regulatory Capability Development and Knowledge Management will lead the strategy, design, and execution of programs that build and sustain critical capabilities across Global Regulatory Affairs. You will direct how essential regulatory knowledge is captured, organized, shared, and applied across the organization. Working closely with Regulatory leaders, Takeda colleagues, Human Resources, learning teams, and subject matter experts, you will identify capability and upskilling needs, develop scalable learning solutions, and strengthen workforce readiness, compliance, and knowledge sharing within a regulated environment. This role will also advance Operational Excellence by establishing sustainable processes, tools, and governance that support consistent execution and continuous improvement.
Job description
About the Role
The Director, Regulatory Capability Development and Knowledge Management will lead the strategy, design, and execution of programs that build and sustain critical capabilities across Global Regulatory Affairs. You will direct how essential regulatory knowledge is captured, organized, shared, and applied across the organization. Working closely with Regulatory leaders, Takeda colleagues, Human Resources, learning teams, and subject matter experts, you will identify capability and upskilling needs, develop scalable learning solutions, and strengthen workforce readiness, compliance, and knowledge sharing within a regulated environment. This role will also advance Operational Excellence by establishing sustainable processes, tools, and governance that support consistent execution and continuous improvement.
How You Will Contribute
- Develop and lead the capability development and knowledge management strategy for Regulatory functions, aligning programs with business priorities and future capability needs.
- Establish and apply capability frameworks, role profiles, and skills models that define the critical capabilities required for regulatory processes, leadership, training effectiveness, and operational execution.
- Partner with Regulatory and business leaders, Human Resources, learning teams, and subject matter experts to assess skills gaps and prioritize development needs associated with new and existing processes, systems, and organizational changes.
- Identify critical organizational knowledge and improve understanding of newly designed or evolving processes.
- Design and oversee scalable onboarding, learning, upskilling, and role-based enablement programs that strengthen readiness, adoption, and performance.
- Develop and maintain global frameworks for the capture, curation, classification, retention, and retrieval of regulatory process information, decisions, and program materials.
- Establish standards for capability assessment, learning path design, content development, and program evaluation within regulated environments.
- Partner with Human Resources to integrate capability development into talent processes, including career development, succession planning, performance development, and change-impact mitigation.
- Identify learning opportunities for colleagues and facilitate the capture and sharing of knowledge across the organization, including the management of enterprise professional society memberships.
- Evaluate program effectiveness using learner feedback, proficiency measures, and business outcomes.
- Apply insights in partnership with Operational Excellence colleagues to continuously improve learning and knowledge management solutions.
- Define and monitor metrics for knowledge reuse, content effectiveness, adoption, and business impact.
- Oversee external vendors, consultants, and internal team members supporting capability development, training, knowledge transfer, and knowledge accessibility initiatives.
- Lead the development and management of repositories, collaboration spaces, and supporting tools that provide controlled access, usability, content clarity, and relevance.
- Promote knowledge-sharing behaviors through targeted communications, forums, training, and role-based enablement.
Skills and Qualifications
- Bachelor’s degree in education, organizational development, human resources, business, life sciences, communications, or a related field, or equivalent relevant experience.
- At least 10 years of relevant experience in capability development, knowledge management, learning and development, talent management, organizational effectiveness, or a related discipline within a regulated or global environment.
- This should include at least 5 years of experience in research and development or drug development, preferably within Regulatory Affairs, Clinical Development, Pharmacovigilance, or a related function.
- Demonstrated experience designing and implementing capability frameworks, capability development programs, knowledge repositories, or workforce development initiatives in regulated or highly structured environments.
- Experience partnering with senior leaders and cross-functional stakeholders in complex organizations undergoing process, system, or operating model changes.
- Knowledge of adult learning principles, curriculum design, assessment methods, learning measurement practices, and role-based enablement.
- Understanding of content governance, taxonomy, information architecture, document lifecycle practices, and controlled-documentation principles.
- Working knowledge of Regulatory, Quality, or compliance-focused processes, including inspection readiness and traceable documentation.
- Experience using learning management systems, talent platforms, and knowledge or collaboration tools, such as Microsoft SharePoint and Microsoft Teams, or comparable technologies, to support development programs and controlled content environments.
- Demonstrated communication, facilitation, and stakeholder-management skills, with the ability to support change adoption across a complex organization.
Requirements
- Bachelor’s degree in education, organizational development, human resources, business, life sciences, communications, or a related field, or equivalent relevant experience
- At least 10 years of relevant experience in capability development, knowledge management, learning and development, talent management, organizational effectiveness, or a related discipline within a regulated or global environment
- At least 5 years of experience in research and development or drug development, preferably within Regulatory Affairs, Clinical Development, Pharmacovigilance, or a related function
- Demonstrated experience designing and implementing capability frameworks, capability development programs, knowledge repositories, or workforce development initiatives in regulated or highly structured environments
- Experience partnering with senior leaders and cross-functional stakeholders in complex organizations undergoing process, system, or operating model changes
- Knowledge of adult learning principles, curriculum design, assessment methods, learning measurement practices, and role-based enablement
- Understanding of content governance, taxonomy, information architecture, document lifecycle practices, and controlled-documentation principles
- Working knowledge of Regulatory, Quality, or compliance-focused processes, including inspection readiness and traceable documentation
- Experience using learning management systems, talent platforms, and knowledge or collaboration tools, such as Microsoft SharePoint and Microsoft Teams, or comparable technologies
- Demonstrated communication, facilitation, and stakeholder-management skills, with the ability to support change adoption across a complex organization
Company overview
Takeda Pharmaceutical Company Limited is a Japanese multinational pharmaceutical company founded in 1781 and incorporated in 1925. As one of the world's top 20 largest pharmaceutical companies by revenue and the third largest in Asia, Takeda specializes in developing and commercializing innovative medicines across several therapeutic areas including oncology, rare diseases, neuroscience, gastroenterology, plasma-derived therapies, and vaccines. With approximately 49,095 employees globally, the company operates research and development centers, manufacturing facilities, and commercial operations across 39 U.S. states and numerous countries worldwide. Takeda maintains dual headquarters in Tokyo and Osaka, Japan, with significant operations in Cambridge, Massachusetts, where it serves as the largest life sciences employer in the state. The company's patient-focused approach is guided by its Takeda-ism values of Integrity, Fairness, Honesty, and Perseverance, emphasizing a commitment to delivering life-transforming treatments while advancing sustainable healthcare solutions. Takeda's extensive portfolio includes both innovative biologics and small molecule drugs, supported by strategic acquisitions and partnerships that have expanded its capabilities in areas such as immuno-oncology and rare disease treatments.