Sr Director Strategic Platform Execution

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Date: Aug 21, 2026

Location: Lakewood, CO, US

Company: Terumo BCT, Inc.

Requisition ID:  35439  

 

At Terumo Blood and Cell Technologies, our 8,000+ global associates proud to come to work each day, knowing that what we do impacts the lives of patients around the world. For Terumo, for Everyone, Everywhere.

 

We make medical devices and related products that are used to collect, separate, manufacture and process various components of blood and cells. With our innovative technologies and service offerings, we touch a patient’s life every second of every day and are committed to continuing to increase the number of patients we serve. Advancing healthcare with heart.

 

With some of the best and brightest minds in the industry, an unmatched global footprint, comprehensive benefits and a distinct culture, Terumo Blood and Cell Technologies is a great place to work, grow and be part of a team that is focused on making a difference. Join us and help shape wherever we go next. You create your future and ours.

Sr Director Strategic Platform Execution

 

JOB SUMMARY

The Senior Director, Strategic Platform Execution leads a global organization accountable for bringing TerumoBCT's devices, disposables, and software to market. The role reports to the Senior Vice President, R&D and sits on the R&D Leadership Team. It owns how that work is planned, prioritized, sequenced, and delivered across multiple sites, along with the standards and governance that keep delivery predictable, and it is the senior R&D voice on what TerumoBCT builds and in what order. The Senior Director advises executive leadership on long-range strategy and investment, settles competing priorities, and is accountable for the results that follow, from growth in market share to lower cost and stronger product quality in developed and emerging markets. Much of that gets done through others. The functional engineering teams are peers rather than reports, so the work depends on the frameworks this role sets and on the credibility the leader builds with those teams. The same is true of Commercial, including Enterprise Marketing, where this organization is R&D's chief partner. Together they shape roadmaps, product line strategies, and value propositions, and they run Product Lifecycle Management as a shared process across functions. The Senior Director is accountable for turning what Commercial needs into commitments R&D can meet. Strategic Platform Execution is newly formed, and whoever takes it on will help decide how it is built and how TerumoBCT develops products in the years ahead. We welcome candidates who want that scope.

 

ESSENTIAL DUTIES

  • Is the senior authority and "go to" global leader for platform, program, and project execution across the devices, disposables, and software portfolio, and represents the organization on significant matters with internal and external stakeholders
  • Owns planning and decision-making for the portfolio, and advises top management on long-range direction for the global platform strategy
  • Is the primary R&D interface to the Commercial organization, including Enterprise Marketing. Partners with them on roadmapping, product line strategies, value propositions, and cross-functional Product Lifecycle Management, and brings forward new product opportunities with a clear view of value and risk
  • Designs and implements frameworks for R&D operational excellence, including standard methods for project execution, resource use, performance measurement, and continuous improvement
  • Develops, executes, and continuously improves the organization's build, buy, and borrow competency. Sets the criteria that decide when work is insourced, outsourced, or done with a partner, and leads partner selection, integration, and ongoing governance
  • Establishes systematic approaches for portfolio management, resource planning, and program execution, working with the engineering functions across multiple global sites
  • Leads the change management and communication that carry cultural change through global R&D, and adjusts the approach based on how well it takes hold
  • Defines metrics and governance that track operational performance and progress on change, and that reward the way the organization wants to work
  • Determines the structure and staffing this organization requires, and is responsible for reviewing, evaluating, and developing its leaders and teams while working across a global, cross-functional environment
  • Works across regional and functional boundaries to meet business objectives and project timelines
  • Ensures product design and documentation meet FDA and global regulatory requirements, sets standards for technical documentation and product lifecycle management, and leads or sponsors quality system remediation and major quality initiatives
  • Communicates with senior management and external customers on program, strategic, and business matters, and explains complex solutions to both technical and non-technical audiences

 

MINIMUM QUALIFICATION REQUIREMENTS

 

Education

  • B. S. degree in Engineering required
  • M.S. or PhD degree in Engineering combined with management degree preferred

 

Experience

Candidates will be evaluated on the depth and relevance of the following experience:

  • Minimum 15 years of progressive engineering experience, 10 of which have been leading engineering teams, including experience leading other people leaders
  • Minimum of 5 years medical device industry or equivalently regulated industry
  • Size and complexity of the portfolio held, measured by number of concurrent programs, annual revenue supported, and geographic footprint
  • Commercialized products delivered that combine devices, disposables, and software, and the candidate's specific accountability for each
  • Delivery through insourced, outsourced, and partnered development models, including the partners selected, the structures used, and the outcomes achieved
  • Scale and durability of an operating or process change the candidate led, and evidence it remained in place after their involvement ended
  • Direct engagement with FDA or comparable regulatory bodies, including submissions, inspections, or audits, and the candidate's role in each
  • Leaders developed and advanced, and the succession outcomes that followed

 

Skills

  • Credible as both a platform authority and an operational leader, setting portfolio direction while owning the discipline that delivers it
  • Builds R&D operating models, governance, and standards that hold up after individual programs end and leadership changes
  • Deep command of Design Controls and Quality Management Systems, with the standing to lead quality system remediation and defend decisions to regulators
  • Fluent in portfolio and program management methods, and able to apply them at global, multi-site scale
  • Builds and matures build, buy, and borrow capability, setting up sourcing and partnership models and strengthening them over time
  • Structures and governs external development relationships that hold quality, design control, intellectual property, and schedule accountability without giving up internal ownership
  • Sound judgment on platform trade-offs, and able to guide top management on portfolio direction, sequencing, and investment
  • Aligns senior stakeholders across a matrixed, consensus-driven, multi-region organization without relying on line authority
  • Develops senior leaders and builds succession depth for critical roles
  • Connects platform roadmaps to business results such as market share, cost, margin, and time to market
  • Uses performance data to find and close execution gaps rather than to report status
  • Makes trade-off decisions on scope, resources, quality, and risk with incomplete information

 

-Or-

An equivalent competency level acquired through a variation of these qualifications may be considered.

 

PHYSICAL REQUIREMENTS

Typical Office Environment requirements include: reading, speaking, hearing, close vision, walking, bending, sitting, and occasional lifting up to 20 pounds.

 

The physical demands described here are representative of those that must be met by an associate to successfully perform the essential duties of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential duties.

 

Up to 25% international travel required

 

 

Target Pay Range:  $245,900.00 to $307,400.00  -  Salary to be determined by the education, experience, knowledge, skills, and abilities of the applicant, internal equity, and alignment with market data
Target Bonus on Base:  40.0%

 

We anticipate this requisition will be open for a minimum of five days, from    . We encourage your prompt application.

 

At Terumo Blood and Cell Technologies, we provide competitive total reward offerings that consist of compensation, benefits, recognition, along with a wealth of other well-being, work-life and recognition programs which support in unlocking the potential for you and your family. Included in our expansive list of benefits offerings are multiple group medical, dental and vision plans, a robust wellness program, life insurance and disability coverages, also a variety of voluntary programs such as group accident, hospital indemnity, critical illness, pet insurance and much more. To help you save for retirement, we offer a 401(k) plan with a matching contribution and for work-life balance we have vacation and sick time programs for associates. For us, it’s about protecting the personal welfare of our associates and their families, helping to achieve personal goals and offering those extra touches for convenience, security and overall peace of mind.

 

  • Terumo Blood and Cell Technologies is part of Terumo Group, founded in 1921 and headquartered in Tokyo, Japan.
  • In 2024, Terumo Blood and Cell Technologies reached $1.5 billion in revenue.
  • We employ nearly 8,000 associates globally, with global headquarters in Lakewood, CO, U.S., and regional headquarters in Brussels, Buenos Aires, Singapore and Tokyo.
  • We manufacture devices, disposable sets and solutions at our facilities in Belgium, India, Japan, Northern Ireland, the U.S. and Vietnam. Our global presence enables us to serve customers in more than 130 countries.
  • Our core values help set our direction, guide our actions and keep us true to our corporate mission of contributing to society through healthcare.
    • Respect – Appreciative of others
    • Integrity – Guided by our mission
    • Care – Empathetic to patients
    • Quality – Committed to excellence
    • Creativity – Striving for innovation
  • We contribute to the Leukemia and Lymphoma Society (LLS), raising $2.4 million USD since 2025.

 

We are proud to be an Equal Opportunity Affirmative Action Employer.  All applicants will be afforded equal opportunity without discrimination because of race, color, religion, sex, gender identity or expression, sexual orientation, marital status, order of protection status, national origin or ancestry, citizenship status, age, physical or mental disability unrelated to ability, military status or an unfavorable discharge from military service.

 

Terumo Blood and Cell Technologies is committed to providing a safe, healthy and secure working environment. Our Colorado campus locations are tobacco-free workplaces, and we maintain a drug-free workplace and perform pre-employment substance abuse testing and detailed background verification.


Nearest Major Market: Denver

Job Segment: PLM, Medical Device, Testing, Substance Abuse, Behavioral Health, Management, Healthcare, Technology

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