Engineer - NPI Electro Mechanical

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Date: Jan 20, 2026

Location: Lakewood, CO, US

Requisition : 34546

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.

Step into a key role as an Engineer 2 – NPI Electro‑Mechanical
, where you’ll help bring innovative, highly complex electro‑mechanical medical devices from concept to full-scale production. You’ll be part of a collaborative engineering team focused on New Product Introduction and design transfer for low‑to-mid‑volume manufacturing. In this role, you’ll own the engineering execution of your projects and partner closely with cross‑functional teams to turn breakthrough ideas into life‑changing products.

• Supports the manufacturing launch of new/revised products.
• Performs research, design, and development of manufacturing processes including production flow, assembly methods, and production test equipment.
• Designs, implements, and validates high performing processes that assure product quality.
• Partners with Design Team to understand product requirements and supports Design for Manufacturability initiatives.
• Prepares and reviews engineering/technical documents such as reports, SOPs, protocols, MOPs, and validation documentation.
• May provide work direction to production assemblers during design transfer activities.
• Takes initiative and demonstrates inquisitive approaches to solve moderately complex problems, identifying problems, generating alternatives, and recommending solutions.
• Follows department processes and regularly makes recommendations on these processes.
• Follows technical specification requirements, developing reports, charts, and graphs to support project recommendations and responds to questions from technical staff members and management.
• May work with manufacturing and other functional groups on manufacturing and regulatory compliance issues.
• May work with other manufacturing sites, including CMOs.

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

• Minimum 2 years experience.
• Two (2) years of related working experience in HLA/System integration preferred.
• Experience with functional test or manufacturing test systems preferred.

• Understands manufacturing and test equipment concepts, technologies, and techniques and how to apply them to improve quality and efficiency.
• Experience with Solidworks and Minitab preferred.
• Requires interactive skills in cross-functional participation and influence, mentoring and acceptance of guidance, technical leadership, project management, coordination with cross-functional team members including global manufacturing teams, team behavior, provides support for subordinates, junior engineers, technicians, and management.
• Mechanical and electronic ability and aptitude to assist with equipment trouble‑shooting.
• Interfaces with staff, suppliers, and external subject matter experts to resolve technical issues and train and provide work direction to operators and production service technicians.
• Understanding of and adherence to GMP practices and FDA regulations.
• Knowledge and ability to implement FDA or regulatory requirements as necessary.
• Demonstrated…