Senior International Regulatory Affairs Specialist – EMEA

Agilent Technologies

Regulatory Affairs Specialist at Agilent managing international IVD product submissions and ensuring compliance in EMEA. Collaborating with global teams to oversee registrations and regulatory assessments.

Posted 7/30/2026full-timeRemote • 🇮🇹 ItalySenior💰 €45,296 - €70,775 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in Regulatory Affairs with a focus on IVD product registration and compliance, alongside strong analytical and organizational skills to manage multiple responsibilities effectively.

Highest-signal resume keywords

Regulatory ExperienceIVD RegulationsGTS Tool ProficiencyAnalytical ThinkingInterpersonal Communication

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Regulatory Block ManagementIVD Product RegistrationRegulatory Assessment DocumentationProduct Change TrackingRegulatory Standards Interpretation

Soft Skills

CollaborationStrong Organization SkillsCritical Thinking

Tools & Technologies

GTS Tool

Industry Keywords

IVD ProductsMedical Device RegulationsChannel Partner Business Licenses

About the role

Key responsibilities & impact

Create, manage, and ensure closure of daily Regulatory blocks
Become an expert with the GTS tool handling Regulatory release of IVD products
Create, train, and implement tools for accurate tracking of product changes
Collaborate with Global Regulatory Affairs ensuring regulatory assessments of changes is sought, obtained, and documented
Oversight of Channel Partner business licenses and renewals
Oversight of IVD registrations and renewals
Collaborate with Global Regulatory Affairs ensuring timely registration of IVD products and their renewals

Requirements

What you’ll need

A university degree in a relevant field such as Life-Science/Engineer/Law etc.
Significant regulatory experience with a solid understanding of IVD/medical device regulations and registration requirements.
Ability to interpret regulations and standards in relation to specific products.
Excellent interpersonal and communication skills in English
Proven capability in analytical and critical thinking, collaborating across global teams, strong organization skills, ability to run multiple ongoing responsibilities, and driving tasks through to completion.

Benefits

Comp & perks

Agilent Result Bonus
Stock Purchase Plan
Life Insurance
Pension
Healthcare
Employee Assistance Program
Holiday
Company activities