Regulatory Affairs Consultant

Role: Labelling Manager
Duration: 6 Months
Location: 2 days on site at High Wycombe
Responsibilities and Deliverables:
• Regulatory review and approval of product labelling for Cosmetics and other non-OTC classes per the company portfolio in mainly UK & Ireland
• Regulatory review and approval and advertising or promotional copy for Cosmetics and other non-OTC classes mainly in UK & Ireland
• Support the Regulatory team with specific tasks per the needs of the department, which may include claims tracker updates, databases, compliance tasks
• Work with the regulatory team to develop project implementation plans and manage resource planning to ensure on time completion of projects and tasks
• Project management and implementation of regulatory changes to company assets (product label and promotional materials)
• Work with cross functional partners to drive regulatory strategy and implementation
• Regulatory review and approval of key documents before product ap
• Complete market impact assessments
• Portfolio survey (where used of ingredients)
Experience/Qualifications:
• Minimum B.S. Chemistry, Biology, or related fields
• Significant experience in Cosmetic Regulatory affairs mainly with promotional material and artwork review/approval at all stages of life cycle management, with demonstrated accountability of managing multiple brands.
• Well versed with UK ASA, CAP, BCAP Guidance for Advertising, proven record of successful project management of dossiers with ClearCast
• Strong knowledge and application of the UK & EU Cosmetic Product Regulation
• Excellent leadership, communication, and organizational skills
• Attention to detail, effective in written and oral communication
• Works independently to plan, conduct, and manage regulatory projects to meet department and company objectives
• Responsible for identifying, implementing and managing key RA Departmental projects and/or strategies based on both short- and long-term RA Department objectives.