Job Description

Requisition ID: 34982

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.

As a Supplier Quality Engineer II, you’ll play a critical role in ensuring supplier readiness and product success by partnering directly with suppliers to drive process reliability, consistency, and compliance from design transfer through product launch. In this highly collaborative role, you’ll apply your expertise in process controls, validation, auditing, CAPA investigations, and supplier development to proactively identify and resolve quality risks while strengthening scalable, standardized supplier quality practices. You’ll work cross‑functionally and independently, using sound judgment and creativity to adapt proven engineering methods, improve manufacturing capability, and elevate supplier performance—making this an ideal opportunity for a quality professional who thrives on ownership, problem‑solving, and building strong supplier partnerships that enable high‑quality, manufacturable products.

The primary focus of this role will be to ensure suppliers are qualified, capable, and prepared to deliver compliant and manufacturable components prior to design transfer and product launch. This role works cross-functionally and directly with suppliers to improve process reliability, repeatability, controls, and resolution of quality issues, while contributing to standardized and scalable supplier quality processes.

ESSENTIAL DUTIES

• Serves as the supplier quality representative on assigned NPD/NPI Core Teams.
• Engages early in concept and design phases to assess supplier capability, capacity, and risk.
• Provides Design for Manufacturability (DFM) and supplier readiness input to support production-scale feasibility.
• Tracks and closes supplier-related deliverables and action items.
• Supports supplier selection, evaluations, and qualification activities for components, OEM products, and contract manufacturing services.
• Defines and executes component and process qualification strategies, including validation and verification activities.
• Collaborates with suppliers to identify and close gaps related to process capability, validation, controls, or documentation.
• Manages Supplier Corrective Action Requests (SCARs) and supports corrective and preventive action activities.
• Drives supplier readiness and risk assessments prior to design transfer and launch.
• Partners with Procurement, Operations, Manufacturing, and Quality to ensure effective handoff from development to production.
• Approves disposition of nonconforming product and facilitates implementation of supplier product or process changes.
• Monitors supplier quality performance using defined metrics and data analysis.
• Works on-site at suppliers, as needed, to address quality or delivery concerns and support continuous improvement initiatives.
• Applies statistical tools such as process capability analysis, equivalence testing, and measurement system analysis (e.g., Gage R&R).
• Adheres to standardized global GSQ-NPI and Supplier Quality procedures, tools, and documentation requirements.
• Maintains accurate and compliant project records, qualification reports, and technical documentation in accordance with regulatory expectations.
• Contributes to the development, standardization, and continuous improvement of scalable supplier quality processes through lessons learned, kaizen activities, and cross-functional feedback.
• Performs ISO 13485 and/or ISO 9001-based supplier audits and other supplier capability assessments.
• Knowledge of plastic injection molding, extrusion, thermoforming and other relevant manufacturing processes.
• Work assignments may require additional development or broadening of in-depth engineering skill(s).
• May work with manufacturing and other functional groups on manufacturing and regulatory compliance issues.
• Works cooperatively and effectively across teams to achieve common goals and quality outcomes.

MINIMUM QUALIFICATION REQUIREMENTS

Education

• Bachelor’s degree or equivalent of education and experience sufficient to successfully perform the essential functions of the job may be considered.
• Bachelor of Science Degree in Engineering, preferred.

Experience

• Minimum 4 years of relevant experience.
• Two years of GMP manufacturing experience in a regulated industry or similar field.

Skills

• Project management and coordination with cross-functional team members.
• Understanding of GD&T, Gage R&R, and Correlation studies.
• Qualified Lead Auditor (ISO13485).
• Understanding of and adherence to GMP practices and FDA regulations.
• Continuous improvement mindset, e.g. LEAN, Six Sigma.
• Provides support for technicians, quality specialists, and management.
• Interfaces with staff, suppliers, and external subject matter experts to resolve technical issues.
• Knowledge and ability to implement FDA or regulatory requirements as necessary.
• Demonstrated ability to communicate effectively both verbally and in writing.
• Knowledge and use of relevant PC software applications and databases, and skills to use them effectively.
• Solves moderately complex problems, identifying problems, generating alternatives and recommending solutions.

-Or-

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

LOCATION

Lakewood, Colorado - Onsite (hybrid) - Open to candidates willing to relocate to the area.

TRAVEL

May require up to 20% travel based on business needs.

PHYSICAL REQUIREMENTS

• General Labor Environment requirements include use of personal protective equipment, reading, speaking, hearing, walking, bending, standing, stretching/reaching, hand/finger dexterity, and occasional lifting up to 50 pounds, or transporting up to 500 pounds via carts or mechanized equipment.
• 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.

Target Pay Range: $81,700.00 to $102,100.00 - 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: 7.0%

We anticipate this requisition will be open for a minimum of five days, from April 30, 2026. 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.