Global Regulatory Affairs Lead — International Strategy

Page Executive

Barcelona

On-site

EUR 90,000 - 120,000

Full time

4 days ago

Be an early applicant

Application generator

Turn this role into an interview — a resume and cover letter built around what this employer wants.

Get past ATS filters

Job summary

Page Executive is seeking a senior Regulatory Affairs professional to shape strategic regulatory initiatives for an expanding pharmaceutical portfolio. You will lead international registrations and lifecycle management, coordinating with R&D, Quality, Medical Affairs, and commercial teams to drive timelines and compliance.

The role offers the opportunity to influence regulatory strategy in a transforming, globally active company with a broad Rx/OTC footprint across multiple markets.

Qualifications

8–15 years of experience in Regulatory Affairs within the pharmaceutical industry.
Proven track record managing international registrations and lifecycle activities.
Experience developing and implementing regulatory strategies for development and marketed products.
Experience coordinating activities across international markets with external partners.

Responsibilities

Define and execute regulatory strategies for development and marketed products across global markets.
Lead planning and execution of registrations, variations, renewals and lifecycle management.
Monitor regulatory timelines, risks and deliverables across projects.

Skills

Regulatory strategy

Stakeholder management

Cross-functional leadership

International regulatory coordination

Project management

English fluency

Job description

The role offers the opportunity to influence regulatory strategy in a transforming, globally active company with a broad Rx/OTC footprint across multiple markets.

Get your free, confidential resume review.

or drag and drop your file here.