Remote Product Security Risk Analyst - Medical Devices

SQUAD - Cabinet de conseils et d’expertises; Spain; Remote; EUR 45,000 - 60,000; Full time

Benefits offered by this job

Remote work

Job summary

SQUAD Group is hiring a Product Security Risk Analyst to perform SRAs on R&D medical device products, aligning with AAMI TIR57:2016 and IEC 62304 considerations. The role supports a global leader in in vitro diagnostics and is 100% remote.

You will gather requirements, scope assessments, run workshops, analyze architecture changes, and report results to stakeholders, contributing to KPI tracking and monthly reviews.

Qualifications

• 3+ years in product security or risk analysis.
• Degree or Master’s in engineering, CS or cybersecurity.
• Hands-on experience with AAMI TIR57:2016.
• Solid knowledge of IEC 62304 for medical device software lifecycle.
• Proven experience conducting Product Security Risk Assessments.
• Ability to facilitate technical workshops and communicate findings to R&D teams.
• Strong analytical and technical writing skills.
• Fluent English; French is a strong plus.
• Experience in medical devices/healthcare is a plus.

Responsibilities

• Gather requirements from the client’s Cybersecurity R&D Center of Expertise.
• Scope and plan Product Security assessments.
• Prepare and lead workshops with R&D teams.
• Perform the various categories of Security Risk Assessments requested.
• Analyze the cybersecurity impact of architecture changes.
• Integrate vulnerability scanner results into the risk analysis.
• Create, update, and review SRAs.
• Present and report assessment results to stakeholders.
• Contribute to KPI tracking.
• Participate in the monthly committee with the Cybersecurity R&D Center of Expertise.

Skills

Product security

Security risk analysis

Workshop facilitation

Analytical writing

Stakeholder communication

English fluency

French a plus

Education

Engineering degree

Master's in CS/Cybersecurity

Job description

SQUAD Group is hiring a Product Security Risk Analyst to perform SRAs on R&D medical device products, aligning with AAMI TIR57:2016 and IEC 62304 considerations. The role supports a global leader in in vitro diagnostics and is 100% remote.

You will gather requirements, scope assessments, run workshops, analyze architecture changes, and report results to stakeholders, contributing to KPI tracking and monthly reviews.