V

Verathon

Bladder measurement and airway visualization devices

Cybersecurity Engineer

Full-TimeUpdated on 10/5/2026Deadline 7/31/27
$147.5k - $182k+ Annual bonus
Senior
Bachelor's
Bothell, WA, USA
In Person

About the job

Requirements
  • A bachelor's degree in Systems Engineering, Electrical Engineering, Computer Engineering, or a related technical discipline is required.
  • At least 5 years of demonstrated experience in cybersecurity engineering, product security engineering, or a related field, including at least 3 years focused on cybersecurity for connected or regulated products.
  • Demonstrated experience with system-level threat modeling methodologies such as STRIDE, PASTA, or TARA as defined in IEC 81001-5-1 or AAMI SW96.
  • Working knowledge of medical device cybersecurity regulatory requirements, including FDA premarket and postmarket cybersecurity guidance, IEC 81001-5-1, AAMI SW96, and IEC 62443.
  • Experience defining security requirements and producing verification evidence in a regulated product development environment.
  • Experience with CVE/NVD triage and vulnerability impact assessment at the system level, including CVSS-based vulnerability scoring and cybersecurity risk assessment methodologies.
  • Working knowledge of networking fundamentals, including ports, protocols, and firewalls, and OS-level security concepts across Linux and/or Windows environments relevant to connected medical devices.
  • Working knowledge of architecture and modeling tools such as Visio, PlantUML, or basic SysML for producing security architecture and threat-model artifacts.
  • Strong written communication skills and demonstrated ability to produce clear, audit-ready technical documentation.
Responsibilities
  • Define product security architecture, including identification of software and hardware assets, trust boundaries, control objectives, and interface documentation; specify and review designs for authentication, authorization, cryptography, secure update mechanisms, event logging, data integrity, and system hardening, including STIG-based hardening where applicable.
  • Lead system-level threat modeling, such as STRIDE or MITRE ATT&CK for ICS, and allocate mitigations across hardware, firmware, and software; ensure trust-boundary assumptions are explicit, traceable, and testable.
  • Derive cybersecurity requirements from FDA guidance and consensus standards, including IEC 62443, IEC 81001-5-1, and AAMI SW96; define verification strategies specifying required evidence, timing, and ownership.
  • Produce and maintain design-level product security documentation, including architecture views, control rationale, security requirements traceability matrices, and interface/external connection records.
  • Own the engineering interface during penetration testing and other third-party security engagements by leading scope clarification, environment setup, and technical Q&A; assess the design impact of findings, define the technical remediation approach, and support retest readiness.
  • When post-release remediation is required, define the technical scope and verification approach; coordinate with engineering and release functions to ensure validated deployment and documentation closure.
  • Lead interoperability security assessments for device interfaces with external systems, networks, and devices; evaluate security and safety risks across normal and fault operating modes and define appropriate risk controls for interface trust boundaries.
  • Conduct CVE impact analysis for fielded products; assess the applicability of newly disclosed vulnerabilities to system-level components and architecture; support prioritization and remediation scoping.
  • Contribute to release readiness for security-driven sustaining updates, including inputs to patch packaging, documentation updates, and design change records.
  • Collaborate with Software to ensure security requirements are correctly allocated and verification evidence is complete across the system.
  • Work cross-functionally across Systems, Software, Quality, and Regulatory disciplines to align on security architecture decisions and ensure consistent implementation.
  • Own and maintain the Product Security Management Plan and associated Product Security Management File, ensuring all required cybersecurity activities are planned, traceable, and audit-ready.
  • Support Verathon's Quality Management System, including participation in design reviews, ECO procedures, and DHF/regulatory submission artifact preparation.
  • Stay current with evolving FDA cybersecurity guidance, EU MDR and MDCG 2019-16, NIST CSF, and relevant medical device security standards; identify implications for Verathon products and processes.
Desired Qualifications
  • Experience with FDA QSR/ISO 13485 QMS is preferred.
  • Experience supporting or managing third-party penetration testing engagements, including findings triage and remediation scoping, is strongly preferred.
  • A relevant security certification such as CISSP, CISM, CEH, CompTIA Security+, or equivalent is preferred; candidates with equivalent demonstrated experience will be considered.
  • Familiarity with SBOM concepts and supply chain security considerations for medical devices is an asset.

About the company

Verathon makes medical devices that help clinicians assess and manage patients. Its main products are the BladderScan, a noninvasive ultrasound tool that estimates bladder volume, and the GlideScope video laryngoscope, which provides a live view of the airway during intubation. The BladderScan uses ultrasound to measure the bladder without penetration, and the GlideScope uses a camera on a slim scope to show the airway on a screen. The company differentiates itself with a focused, proven portfolio and a global footprint in more than 70 countries, aiming to improve patient care by offering accurate, noninvasive tools and clearer airway visualization that support better clinical decisions and reduce unnecessary procedures.

Company Size

501-1,000

Company Stage

N/A

Total Funding

N/A

Headquarters

Bothell, Washington

Founded

1984

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Simplify's Take

What believers are saying

  • Verathon launched CFlex on May 15, 2026, entering two-million-plus annual U.S. cystoscopy procedures.
  • SamplePro launched May 21, 2026, strengthening ICU bronchoscopy workflow and cross-sell into BFlex 2 accounts.
  • Verathon's August 25, 2026 newsroom shows continued product cadence, supporting revenue momentum under Roper.

What critics are saying

  • April 2024 GlideScope Core monitor recall remains open, threatening hospital trust and sales cycles.
  • Ambu, Stryker, and Olympus squeeze Verathon's airway and endoscopy pricing through faster innovation.
  • Single-use plastics backlash and hospital cost scrutiny pressure CFlex and BFlex adoption through 2027.

What makes Verathon unique

  • GlideScope, BladderScan, and CFlex span airway, urology, and single-use endoscopy workflows.
  • May 2026 CFlex extends Verathon into cystoscopy with 510(k)-cleared single-use flexible design.
  • May 2026 SamplePro deepens BFlex 2 integration with closed-system bronchoscopy specimen collection.

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Benefits

Health Insurance

Dental Insurance

Vision Insurance

Life Insurance

Paid Holidays

Paid Time Off

401(k) Company Match

Performance Bonus

Tuition Reimbursement

Growth & Insights and Company News

Headcount

6 month growth

↑ 6%

1 year growth

↑ 6%

2 year growth

↑ 5%
The National Law Review
May 21st, 2026
Verathon expands airway portfolio with SamplePro(TM) for BFlex(TM) 2, delivering a spill-proof specimen collection system.

Verathon expands airway portfolio with SamplePro(TM) for BFlex(TM) 2, delivering a spill-proof specimen collection system. Designed to protect the specimen and reduce handling risk in ICU bronchoscopy BOTHELL, WA, UNITED STATES, May 21, 2026 /EINPresswire.com/ - Verathon(R), a global medical device company known for its GlideScope(R) and BFlex(TM) brands, today announced the U.S. launch of SamplePro(TM), an integrated closed-system specimen collection solution purpose-built for the BFlex(TM) 2 single-use bronchoscopy platform. SamplePro extends Verathon's leading airway portfolio with a self-sealing sampling solution that protects the collected specimen while safeguarding clinicians and patients. In ICU bronchoscopy, specimen collection during bronchoalveolar lavage (BAL) and bronchial wash (BW) procedures has long depended on traditional specimen traps such as the Lukens trap. These methods require disconnecting suction tubing between collection modes, which can interrupt workflow, raise the risk of cross-contamination, and lead to specimen loss from spillage. Newer alternatives have addressed the tubing problem, but they still rely on open containers or manual locks, leaving the system partially exposed. SamplePro addresses that gap with self-sealing valves that maintain a closed system. What SamplePro delivers for ICU teams: - Specimen security: Self-sealing containers maintain a closed system from collection through detachment, protecting the collected specimen from spills and the user from exposed pathogens. - Simplified workflow: An easy click-and-connect setup reduces time spent preparing the equipment and switching between sampling containers. - Strong clinician preference: In a recent study, 100% of providers rated SamplePro's collected specimen security as excellent/good, and 85% reported a better sampling workflow compared to their existing device. Purpose-built for the BFlex 2 platform, SamplePro integrates with the bronchoscope to support consistent and reliable sampling, even when managing difficult secretions. Together, BFlex 2 and SamplePro create a fully integrated bronchoscopy workflow designed to reduce disruption during specimen collection. "Specimen collection has always been one of the more vulnerable steps in bronchoscopy, with open containers, tubing changes, and the risk of losing what you just collected," said Ashley Smith, VP of Airway. "SamplePro transforms the collection process. The system stays closed through the entire procedure, which reduces a real source of variability when specimen integrity matters." The bronchoscopy market continues to evolve toward more integrated, procedure-focused solutions designed to improve workflow consistency, simplify handling, and support ICU efficiency. Innovations like SamplePro reflect the ongoing industry focus on advancing bronchoscopy workflows through more streamlined, connected, and clinician-centered procedural technologies. SamplePro for BFlex 2 is now available in the United States, with additional markets to follow. Availability may vary by region. For more information or to request a demonstration, visit verathon.com/airway. About Verathon Verathon(R) is a global medical device company dedicated to advancing single-use endoscopy and point-of-care visualization for airway management and urology. Its GlideScope(R) video laryngoscopes, BFlex(TM) bronchoscopes, BladderScan(R) bladder volume systems, and CFlex(TM) single-use flexible cystoscopes are designed to help clinicians improve workflow efficiency and patient care. Headquartered in Bothell, Washington, and operating across North America, Europe, and Asia, Verathon is a business unit of Roper Technologies. Comparative and performance claims are based on internal bench testing data on file at Verathon. Erna Kristinsdóttir Verathon +1 425-588-1587 email us here Visit us on social media: LinkedIn Instagram Facebook YouTube X Legal Disclaimer: EIN Presswire provides this news content "as is" without warranty of any kind. We do not accept any responsibility or liability for the accuracy, content, images, videos, licenses, completeness, legality, or reliability of the information contained in this article. If you have any complaints or copyright issues related to this article, kindly contact the author above.

Associated Press
May 15th, 2026
Verathon launches CFlex single-use flexible cystoscope with 70% more flow during instrument use

Verathon, a global medical device company, has launched CFlex, an FDA 510(k)-cleared single-use flexible cystoscope in the United States. The product marks the company's expansion into cystoscopy procedures, extending its urology portfolio beyond its existing BladderScan brand. CFlex is designed to address common cystoscopy challenges with integrated adapters, up to 70% more irrigation flow during instrument use compared with other single-use cystoscopes, and high-contrast imaging. The device features a 15 Fr insertion tube and 210-degree bidirectional articulation for improved manoeuvrability. The single-use design eliminates reprocessing requirements and scope repair cycles. CFlex incorporates sustainability features including a reusable cable and a handle manufactured with 80% bio-based plastics. The product was featured at the American Urological Association Annual Meeting in Washington, D.C., in May 2026.

The National Law Review
May 15th, 2026
Verathon Expands urology portfolio with CFlex(TM), its first single-use flexible cystoscope.

Verathon Expands urology portfolio with CFlex(TM), its first single-use flexible cystoscope. Designed to simplify setup, improve visualization, and expand maneuverability in cystoscopy procedures. BOTHELL, WA, UNITED STATES, May 15, 2026 /EINPresswire.com/ - Verathon(R), a global medical device company known for its GlideScope(R), BFlex(R), and BladderScan(R) brands, today announced the U.S. launch of CFlex(TM), an FDA 510(k)-cleared single-use flexible cystoscope. CFlex extends Verathon's urology portfolio into cystoscopy, applying the company's single-use endoscopy experience to a design built for cystoscopy workflow. The product will be featured at the Verathon Booth (#807) at AUA 2026 in Washington, D.C., May 15-18. In both office and operating room settings, cystoscopy can be slowed by setup complexity, reduced irrigation flow during instrument use, and visualization challenges that extend procedure time. CFlex is engineered to address these challenges with integrated adapters, up to 70% more flow during instrument use compared with other currently available single-use cystoscopes, and high contrast imaging. Additionally, it features a tapered, slim 15 Fr insertion tube designed to support patient comfort. What CFlex delivers for urologists: - Reduces setup steps and supports clinician control of flow with a dedicated irrigation inlet, built-in adapters, and fingertip flow control, with fewer hand-offs during setup. - Provides up to 70% more flow when an instrument is inserted1. Its larger (7.2 Fr) channel delivers more irrigation, helping maintain a clear field in cloudy or bloody environments. - Supports clear visualization of anatomy with high-contrast imaging and accurate color. - Expands the field of view and supports access across the bladder with 210° bidirectional articulation, which can help reduce the need for repositioning. Beyond the scope itself, CFlex is designed for the full procedure; it pairs with Verathon's CystoView 15-inch Full HD monitor and a cystoscopy cart for quick setup across office and OR environments. Because every case starts with a new scope, CFlex eliminates reprocessing and scope repair cycles, removing a common source of case delays and reducing the risk of cross-contamination. CFlex also reflects Verathon's continued focus on sustainability, featuring a reusable cable to help reduce waste and a handle manufactured with 80% bio-based plastics calculated via the mass balance approach. Cystoscopy volumes in the U.S. are estimated to exceed two million procedures annually, with a growing share performed in office-based settings where setup speed and workflow simplicity are at a premium. CFlex is purpose-built for this shift. "CFlex marks the next chapter for our urology business," said Parimal Shah, SVP, Urology Business Unit at Verathon. "We built a urology presence with BladderScan(R) and a single-use endoscopy platform with GlideScope(R) and BFlex(R). CFlex brings those together, and it's the first of a broader urology portfolio." Verathon will feature CFlex at Booth #807 during the 2026 American Urological Association Annual Meeting (AUA2026) at the Walter E. Washington Convention Center in Washington, D.C., May 15-18. Attendees can see live demonstrations, get hands-on previews, and meet with Verathon's urology team. The CFlex Single-use Cystoscope is a sterile, single-use, flexible cystoscope intended for endoscopic access to and examination of the lower urinary tract in adult patients. CFlex is 510(k) cleared by the U.S. Food and Drug Administration and is now available in the United States. For more information or to request a demonstration, visit verathon.com/urology. About Verathon Verathon(R) is a global medical device company dedicated to advancing single-use endoscopy and point-of-care visualization for airway management and urology. Its GlideScope(R) video laryngoscopes, BFlex(R) bronchoscopes, BladderScan(R) bladder volume systems, and CFlex(TM) single-use flexible cystoscopes are designed to help clinicians to improve workflow efficiency and patient care. Headquartered in Bothell, Washington, and operating across North America, Europe, and Asia, Verathon is a business unit of Roper Technologies. Comparative and performance claims are based on internal bench testing data on file at Verathon. Legal Disclaimer: EIN Presswire provides this news content "as is" without warranty of any kind. We do not accept any responsibility or liability for the accuracy, content, images, videos, licenses, completeness, legality, or reliability of the information contained in this article. If you have any complaints or copyright issues related to this article, kindly contact the author above.

EIN News
Aug 1st, 2025
Verathon Launches GlideScope ClearFit Video Laryngoscope Offering Cost-Effective Airway Management

Verathon launches GlideScope ClearFit video laryngoscope offering cost-effective airway management.

Medical Device Network
Nov 28th, 2024
Verathon launches sustainable single-use laryngoscope

Roper Industries acquired Verathon in 2009 from DW Healthcare Partners in a deal worth around $300m.