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Medical Device Cybersecurity Jobs in Remote, OR (NOW HIRING)

Demonstrated experience supporting or leading cybersecurity activities for medical device or other regulated product development programs. * Strong communication, collaboration, stakeholder ...

... medical device, or healthcare IT). * Strong understanding of IT roles such as software engineering, data science, cloud, infrastructure, cybersecurity, and systems supporting clinical or R&D ...

Partner with the CTO on architecture, data governance, AI model decisions, and FDA cybersecurity ... Familiarity with FDA regulatory pathways for Software as a Medical Device (SaMD) or 510(k)

Medical Device Cybersecurity information

See Remote, OR salary details

$21

$49

$96

How much do medical device cybersecurity jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for medical device cybersecurity in Remote, OR is $49.79, according to ZipRecruiter salary data. Most workers in this role earn between $35.05 and $59.57 per hour, depending on experience, location, and employer.

What are some common challenges faced by professionals in medical device cybersecurity, and how can they be addressed?

Professionals in medical device cybersecurity often encounter challenges such as integrating security measures into legacy devices, ensuring compliance with evolving regulations, and balancing usability with robust protection. Collaborative efforts with engineering, regulatory, and clinical teams are crucial to embedding security throughout the product lifecycle. Staying current with threat intelligence and participating in cross-functional risk assessments also help anticipate and address vulnerabilities proactively.

What is medical device cybersecurity?

Medical device cybersecurity refers to the protection of medical devices and the data they process from cyber threats and unauthorized access. As medical devices become increasingly connected to hospital networks and the internet, robust cybersecurity measures are essential to ensure patient safety and protect sensitive health information. This field involves identifying vulnerabilities, implementing safeguards, and complying with regulatory requirements to reduce the risk of cyberattacks on medical technology.

What is the difference between Medical Device Cybersecurity vs Medical Device Quality Assurance?

AspectMedical Device CybersecurityMedical Device Quality Assurance
Required CredentialsCertifications in cybersecurity, such as CISSP or CISA; knowledge of medical device regulationsCertifications in quality management, like CQE or ISO 13485 auditor
Work EnvironmentIT security teams, R&D, regulatory compliance in healthcare settingsManufacturing, clinical, and regulatory environments focused on product quality
Employer & Industry UsageMedical device manufacturers, healthcare providers, cybersecurity firmsMedical device companies, regulatory agencies, quality assurance firms

Medical Device Cybersecurity focuses on protecting medical devices from cyber threats, ensuring data integrity and security. Medical Device Quality Assurance emphasizes maintaining product quality, safety, and compliance throughout development and manufacturing. While both roles support patient safety, cybersecurity specialists address digital vulnerabilities, whereas quality assurance professionals ensure the device meets regulatory standards.

What are the key skills and qualifications needed to thrive in medical device cybersecurity, and why are they important?

To thrive in Medical Device Cybersecurity, you need a solid background in cybersecurity principles, risk management, and biomedical engineering, often supported by a relevant degree and certifications like CISSP or CISM. Familiarity with regulatory standards (such as FDA cybersecurity guidelines), network security tools, and vulnerability assessment systems is essential. Strong analytical thinking, attention to detail, and effective communication skills help professionals collaborate with cross-functional teams and address complex security challenges. These skills are crucial to ensure medical devices remain secure from cyber threats, protecting patient safety and maintaining regulatory compliance.
What are popular job titles related to Medical Device Cybersecurity jobs in Remote, OR? For Medical Device Cybersecurity jobs in Remote, OR, the most frequently searched job titles are:
What job categories do people searching Medical Device Cybersecurity jobs in Remote, OR look for? The top searched job categories for Medical Device Cybersecurity jobs in Remote, OR are:

Product Cybersecurity Architect

Bausch + Lomb

OR • On-site, Remote

Full-time

Dental, Vision, Life, Retirement, PTO

Posted 29 days ago


Bausch & Lomb rating

8.6

Company rating: 8.6 out of 10

Based on 39 frontline employees who took The Breakroom Quiz

22nd of 538 rated manufacturers


Job description

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world-from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better.
Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future.
Why this Role Matters
Join the Surgical R&D organization in a role where you will help ensure the cybersecurity, safety, and reliability of innovative surgical products that support patient care. In this position, you will be responsible for embedding secure-by-design practices throughout the product lifecycle while partnering with engineering, quality, regulatory, and corporate security teams to deliver compliant and resilient solutions. This is a strong opportunity for someone who brings deep product security expertise, strong cross-functional collaboration skills, and a passion for advancing cybersecurity within a regulated medical device environment.
What You'll Do
  • Architect and implement a consistent cybersecurity strategy across surgical capital equipment product lines to establish a scalable and secure product ecosystem.
  • Embed secure-by-design principles throughout the product lifecycle, providing guidance on secure architecture, threat modeling, design controls, cryptography, and secure communication protocols.
  • Lead execution of cybersecurity requirements across development programs, ensuring alignment with regulatory expectations, corporate standards, and product quality objectives.
  • Coordinate vulnerability management activities, including intake, triage, risk assessment, remediation tracking, and documentation of product security issues through closure.
  • Serve as the Surgical R&D cybersecurity representative for vulnerability disclosure and incident response activities, supporting investigations, impact assessments, root cause analyses, and remediation efforts.
  • Partner with engineering teams to implement security testing practices, including SAST, DAST, SCA, penetration testing, and automated security controls within development pipelines.
  • Support supplier and third-party security initiatives by defining security requirements, managing software supply chain risks, and maintaining Software Bill of Materials (SBOM) processes.
  • Collaborate with Quality, Regulatory Affairs, IT, and Corporate Product Security teams to ensure compliance with evolving cybersecurity regulations and industry standards while enabling efficient product delivery.

What You'll Bring
Required Education & Experience:
  • Bachelor's degree in Engineering, Computer Science, Cybersecurity, or a related technical discipline.
  • 7+ years of experience in product security, application security, medical device cybersecurity, or software security within a regulated environment.
  • Demonstrated experience supporting or leading cybersecurity activities for medical device or other regulated product development programs.
  • Strong communication, collaboration, stakeholder management, and problem-solving skills.
  • Ability to translate technical cybersecurity risks into clear, actionable guidance for engineering, quality, and regulatory stakeholders.

Specialized Technical, Regulatory & Industry Skills & Knowledge
  • Strong expertise in secure product design, threat modeling, vulnerability management, and secure software development practices.
  • Working knowledge of connected device security, embedded systems, and software-enabled product architectures.
  • Experience with security testing tools and methodologies, including SAST, DAST, SCA, and penetration testing.
  • Understanding of software supply chain security practices, including SBOM development and third-party risk management.
  • Experience working across cross-functional and global teams to drive cybersecurity outcomes and influence stakeholders without direct authority.
  • Knowledge of secure development lifecycle (SDLC) frameworks, vulnerability disclosure processes, and product incident response activities.
  • Familiarity with cybersecurity governance, risk assessment, and compliance processes within regulated industries.

Preferred
  • Advanced degree in Cybersecurity, Computer Science, Engineering, or a related field.
  • Relevant industry certifications such as CISSP, CSSLP, OSCP, GWAPT, or equivalent.
  • Experience in medical device, healthcare, or other regulated industries, and/or working within a quality-managed or GxP regulated environment.
  • Working knowledge of medical device cybersecurity regulations and standards (e.g., FDA premarket/post market guidance, IEC 81001-5-1, AAMI TIR57, UL 2900, NIST frameworks).
  • Experience developing cybersecurity documentation to support regulatory submissions and audits.

This position may be available in the following location(s): US - Remote
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
For U.S. locations that require disclosure of compensation, the starting pay for this role is between $140,000 and $180,000. The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors.
U.S. based employees may be eligible for short-term and/or long-term incentives. They may also be eligible to participate in medical, dental, vision insurance, disability and life insurance, a 401(k) plan and company match, a tuition reimbursement program (select degrees), company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive sick time, floating holidays and paid vacation.
Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms.
To learn more please read Bausch + Lomb's Job Offer Fraud Statement.
Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

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About Bausch & Lomb

Sourced by ZipRecruiter

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world--from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our nearly 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 12,500 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Bridgewater, NJ, US

Year founded

1853