Senior Regulatory Affairs Manager, EU Procedures

Elanco

. Support regional registration activities for existing animal health products registered in two or more European Economic Area countries or the United Kingdom .

Posted 10/28/2026full-timeHook • United KingdomSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in regulatory affairs within the animal health sector, including the preparation of technical submission packages and coordination of regulatory submissions across European Economic Area countries and the United Kingdom. Proficient in managing timelines and collaborating with cross-functional teams to ensure compliance and maintain marketing authorisations.

Highest-signal resume keywords

Regulatory Affairs ExperienceTechnical Submission PreparationVault RIM ManagementFluent EnglishAnimal Health Industry Knowledge

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Regulatory Submission CoordinationTechnical Submission Package DeliveryProduct Labelling ActivitiesPost-Approval Commitments ManagementLegislation MonitoringDossier PublicationNational Requirements CoordinationFee Payment ManagementProcess Improvement ContributionProject and Budget Forecasting

Soft Skills

Interpersonal SkillsCommunication Skills

Tools & Technologies

Vault RIM

Certifications & Qualifications

Bachelor’s Degree in Veterinary MedicineMaster’s Degree in Related Field

Industry Keywords

Animal HealthEuropean Economic AreaUnited KingdomRegulatory AuthoritiesCross-Functional TeamsResearch and DevelopmentMarketing ComplianceInfectious DiseasesImmunologyBiologics

Tech Stack

Tools & technologies

Vault

About the role

Key responsibilities & impact

Support regional registration activities for existing animal health products registered in two or more European Economic Area countries or the United Kingdom
Coordinate regulatory submissions, product labelling activities and post-approval commitments
Partner with affiliates, global teams and regulatory authorities to maintain marketing authorisations and support continued product supply
Plan, prepare, publish and deliver technical submission packages for European Union and United Kingdom regulatory procedures
Manage regulatory submission timelines, tracking and prioritisation using Vault RIM
Partner with European affiliates, Marketing, Research and Development and other functions to complete national requirements, maintain product labelling and support product compliance
Act as a point of contact for regulatory authorities and support authority meetings, questions and responses, and post-approval commitments
Monitor changes in legislation and regulatory guidance, assess business impact, contribute to process improvements, regulatory advocacy, and project and budget forecasting

Requirements

What you’ll need

Bachelor’s or Master’s degree in veterinary medicine, biologic, infectious diseases, immunology, or a related field
2+ years of experience in regulatory affairs
Fluent English
Ability to prepare and deliver complete, high-quality technical submission packages to competent authorities
Experience coordinating submission components such as national requirements, translations, fee payments and dossier publication
Experience in the animal health industry preferred
Experience working with cross-functional and international teams across regulatory, Research and Development, Marketing and affiliate organisations preferred
Strong interpersonal and communication skills preferred

Benefits

Comp & perks

Hybrid work model
Around 10% travel
Diverse and inclusive work environment
Opportunities to acquire new skills and experiences
Equal opportunity and affirmative action employer