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.