Product Security Engineer — Interventional Vascular Medical Device (Bedford, MA)

Philips

Closes in 2 days

Quick summary

Work type
On-site
Location
Bedford, MA
Salary
$157,000–$157,000 / yr
Posted
6 days ago
Closes
Jun 17, 2026 (soon)
Nearby
99+ roles within 25 mi

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $176k
This role $157k
$127k most similar roles pay here $216k

This role pays less than 67% of similar roles. Most pay $148,500–$204,500 — the shaded band above. At the midpoint, this role pays about $157k versus about $176k for comparable roles.

Based on 240 similar postings.

Employer

About Philips

Royal Philips (founded 1891) is a leading Dutch health technology company focused on improving well-being through innovation, transitioning from a diversified electronics giant to a specialist in healthcare, imaging, patient monitoring, and personal health.

Philips currently has 12 open roles on FindRole.

Listed pay typically runs $115,000–$182,000 across 12 roles with salary data.

Most-posted roles

View all roles at Philips

At a glance

TL;DR · Product Security Engineer — Interventional Vascular Medical Device (Bedford, MA)

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As a Product Security Engineer at Philips in Bedford, MA, you will lead the Secure Product Development Lifecycle (SPDLC) for interventional vascular medical devices, defining and maintaining standards that ensure regulatory compliance and patient safety. Your daily responsibilities include driving secure design practices, threat modeling, and vulnerability management across engineering teams, while continuously integrating new tools and industry standards to enhance security. You will collaborate with R&D, quality, and regulatory teams to produce cybersecurity documentation and manage vulnerabilities, ensuring a balance between security, usability, and time-to-market. Ideal candidates have 5+ years of experience in product/application security or embedded systems security, expertise in medical device cybersecurity standards (IEC 81001-5-1, AAMI TIR57), and strong technical writing skills for regulatory documentation.

Skills

IEC_81001-5-1 AAMI_TIR57 FDA_guidance IEC_62304 SBOM_management ISO_14971 ISO_13485 21_CFR_820 CISSP CSSLP GIAC OSCP Secure_Product_Development_Lifecycle Threat_Modeling Secure_Coding Vulnerability_Assessment Penetration_Testing Technical_Writing Regulatory_Documentation

What you'll do

  • Define and maintain Secure Product Development Lifecycle (SPDLC) standards for medical devices.
  • Implement SPDLC practices across engineering teams, including secure design and threat modeling.
  • Continuously update security practices with new tools and industry standards.
  • Lead threat modeling and security risk assessments throughout the product lifecycle.
  • Ensure regulatory compliance by producing cybersecurity documentation and managing vulnerabilities.

What we're looking for

  • 5+ years of experience in product/application security or embedded systems security.
  • Expertise in secure development lifecycle (SDL) processes and threat modeling.
  • Knowledge of medical device cybersecurity standards and regulatory compliance.
  • Experience with SBOM management, ISO 14971/13485, and 21 CFR 820.
  • Bachelor’s degree in Computer Science, Engineering, Cybersecurity or related field.
  • Strong technical writing skills for regulatory documentation.

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