Overview
In this role you will shape global regulatory strategy for a diverse Consumer Health portfolio, guiding products from development to post-approval across markets. You will collaborate with global and local teams to secure approvals and maintain licenses, driving compliant market access. The position offers a global arena to influence regulatory decisions that impact millions of consumers. You will work in a cross-functional, matrix environment, delivering practical regulatory solutions and enabling innovation.
Pay / Benefits
- hybrid working
- private healthcare
- pension scheme
- life insurance
- wellness programs
- volunteering days
Responsibilities
- Develop and deliver global regulatory strategies across the product lifecycle, supporting innovation, launches, rollouts, and post-approval activities
- Lead regulatory submissions and registrations with affiliates to secure timely approvals and maintain marketing authorisations
- Prepare, maintain, and oversee regulatory dossiers and documentation ensuring compliance across markets
- Provide regulatory guidance to cross-functional stakeholders supporting business objectives while addressing health authority requirements
- Collaborate with global Regulatory, Commercial, Quality, Technical, and Scientific teams to ensure successful registration, lifecycle management, and market access
Key requirements
- 3–5 years of Regulatory Affairs experience, ideally within Consumer Health
- Experience supporting regulatory activities for medicinal products, cosmetics, and/or food supplements
- Strong understanding of regulatory submissions, lifecycle management, and global registration requirements
- Excellent communication and stakeholder management skills across countries and functions
- excellent communication
- stakeholder management
- collaborative mindset
- regulatory submissions
- lifecycle management
- global registration requirements
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