Product Security Process Analyst II

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Date: Aug 11, 2026

Location: Lakewood, CO, US

Requisition : 35373

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.

Terumo Blood and Cell Technologies designs, engineers, and builds medical technology that helps save lives. The Product Security Process Analyst II plays a key role in strengthening and sustaining product security governance for regulated medical devices. This role concentrates on interpreting regulatory and industry cybersecurity requirements, assessing their applicability, and shaping how those requirements are implemented, documented, and sustained.

This position partners closely with Product Security Engineers, R&D, Quality, and Regulatory Affairs to translate evolving cybersecurity regulations and standards into clear, auditable, and practical product security processes.

• Serve as a product security process subject‑matter expert, supporting compliance with FDA cybersecurity guidance and global medical device cybersecurity regulations and standards.
• Support the creation, maintenance, and continuous improvement of product security Policy, SOPs, and work instructions.
• Own or support product security quality plans and CAPA activities, including documentation, tracking, and coordination with cross‑functional stakeholders.
• Translate product security requirements into clear, actionable requirements and ensure traceability within the requirements tool.
• Partner with Product Technical Leads, R&D, and Product Security Engineers to ensure product security activities align with quality plans and lifecycle expectations.
• Support internal audits, regulatory agency inspections/audits, and readiness activities related to product security.
• Monitor adherence to defined product security processes and identify gaps or improvement opportunities.
• Act as a connector between Product Security, Quality, and Regulatory teams to ensure consistent execution and communication.

• May be required to travel to other company locations on occasion.

Bachelor’s degree in Engineering, Computer Science, Cybersecurity, Biomedical Engineering, or a related technical discipline, or an equivalent combination of education and relevant experience sufficient to perform the essential functions of the role.

• Minimum 5 years of experience in Systems Engineering, Software Development, or Cybersecurity in a regulated environment, preferably medical devices.
• Experience working with regulated products, development processes, or quality systems is strongly preferred.

• Strong analytical and written communication skills, with the ability to translate complex requirements into clear guidance.
• Ability to work collaboratively across engineering, quality, regulatory, and security teams.
• Comfortable influencing without direct authority and navigating ambiguity.

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…