Regulatory Affairs Manager Cosmetics

Your new company
Our client is an internationally recognised leader in pharmaceuticals, medical devices, consumer health and related products. They have a need for a contractor for their regulatory team and are seeking a Senior Regulatory Affairs Specialist to drive product approvals and ensure continued compliance across key markets.This is a fantastic opportunity to join a forward-thinking organisation where you'll influence strategy, shape product claims, and ensure successful launches across multiple categories including medicines, cosmetics, medical devices, and food supplements.Your new role
As a Senior Regulatory Affairs Specialist, you will act as the go-to expert for local regulatory requirements, approval pathways and compliance activities. You'll play a pivotal role in ensuring that new product registrations, line extensions and claims align with business goals and regulatory expectations.Key responsibilities include:Regulatory Strategy & Submissions

• Provide expert regulatory guidance to cross-functional product development teams
• Assess quality, preclinical and clinical data packages for submission readiness
• Prepare, compile and submit regulatory dossiers in line with local authority requirements.
• Monitor submission progress and maintain proactive communication with regulatory authorities.
• Evaluate and guide product labelling and claims to ensure full compliance

Regulatory Compliance & Governance

• Maintain up-to-date knowledge of evolving regulatory legislation across relevant markets
• Ensure local compliance with all regulatory and quality system requirements
• Review and approve promotional materials and product artwork
• Support internal and external audits in partnership with Quality teams.
• Identify process improvements and support the implementation of global/regional regulatory initiatives
• Maintain the accuracy of regulatory systems and ensure swift escalation and resolution of compliance concerns

What you'll need to succeed

• Highly knowledgeable in regulatory frameworks for healthcare and consumer products and must have experience working in cosmetics
• Confident working independently and providing authoritative regulatory advice
• Experienced in managing submissions and interacting with Health Authorities

What you'll get in return
Hybrid working pattern, 2 days onsite in Reading
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.

JBRP1_UKTJ