Director, R&D Asset Transition & Integration Office (RATIO)

You will operate at the intersection of science, operations, and strategy—building the capability as well as running it, while maintaining the highest standards of quality and data integrity.

How you will contribute:

As a leader within RATIO, you will:

Lead and develop a team of transition professionals; set objectives, allocate assignments across the book of work, and manage performance, capability and career development

Hold accountability for a portfolio of live transitions, ensuring budgets, schedules and performance standards are realistically set and attained; lean into more complex or sensitive transitions

Own and/or support the design and implementation of a digitized, data-driven transition processes

Drive and/or support process optimization across transition archetypes: standardized playbooks, templates and process maps, defined KPIs, and a continuous improvement cycle informed by structured lessons learned

Govern the operating model, ways of working, and operational agreements between RATIO and the functions it depends on

Provide strategic insight to senior leadership, including portfolio-level status, risk assessment, and resourcing plans

Support build of organizational capability through training curricula, knowledge management, and the development of less experienced colleagues

Ensure compliance and integrity across the portfolio, including contractual obligations, regulatory requirements, safety commitments, and data governance

What Makes This Role Unique:

This role is part of an innovative capability that is leading across the pharma industry. Accordingly, you'll be close to some of the most complex and high-impact work in R&D. You will:

Shape how Takeda executes asset transitions and RATIO shows up as a brand

Lead a team while remaining hands-on with priority transitions

Work across the full breadth of R&D functions rather than within a single discipline

Modernize a capability with current technology and people capabilities and real latitude to design the future state

Represent Takeda to external partners and counterparties at senior level

Success in this role requires someone who has a learning mindset, balances operational rigor with judgement, builds capability in others, and drives alignment across a highly matrixed, global environment.

Minimum Requirements/Qualifications:

Minimum Bachelor's degree in a scientific or related field required; advanced degree welcomed

10+ years of relevant experience in the pharmaceutical or biotech industry, particularly in R&D strategy and operations and/or program management

Demonstrated people management experience, including direct line management

Demonstrated delivery in global matrix environments

Experience working with external counterparties—partners, licensors, CROs, or vendors

Fluent English at a level suitable for global governance forums

Working knowledge of R&D processes, such as clinical development, regulatory, safety, and quality systems

Track record of strong project management and leading complex, cross-functional programs to completion with external counterparties

Demonstrated people leadership (e.g., building, developing and retaining a high-performing team)

Experience designing and implementing improved processes or digital tooling in a regulated environment, with measurable outcomes

Understanding of data and records management, such as regulatory data transfer, system transitions, and archival strategies

Familiarity with global R&D systems and infrastructure, and how they interact during transitions

Strong communication and interpersonal skills and ability to drive a collaborative environment

Ability to navigate ambiguity and drive progress, even in highly complex environments

Preferred:

Experience in any of the following: R&D alliance management, Business Development (e.g., M&A integration, divestment, in-licensing), asset termination, or Life Sciences Strategy or Management Consulting

Experience deploying project and portfolio management platforms (e.g., Planisware), business intelligence and dashboard tooling (e.g., Power BI), workflow automation, or AI-enabled ways of working

Process excellence credentials or equivalent practical experience

Contract literacy

Budget forecasting, tracking and closeout for program spend

Experience working across cultures and time zones

Additional Information:

May require travel, including international travel

This position is currently classified as "hybrid" in accordance with Takeda’s Hybrid and Remote Work policy.

More about us:

At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.

Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

This position is currently classified as "hybrid" following Takeda's Hybrid and Remote Work policy.

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Locations

Lodz, Poland

Base Salary Range:

zł421,400.00 - zł579,480.00

For information about our benefits, please click here.

Locations

Warsaw, PolandLodz, Poland

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time