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Regulatory Affairs Specialist

  1. England, East Anglia
Buckinghamshire
  1. Contract
Competitive
  1. Drug Safety / Pharmacovigilance
35688
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Regulatory Affairs Specialist - Pharmaceuticals - 6-Month Contract 

Do you want to be part of a forward thinking global pharmaceutical client who have facilities in over 60 countries worldwide? Then this is the next step for you! One of our global pharmaceutical clients is currently requiring an experienced Regulatory Affairs Specialist for their Buckinghamshire based location.  


Responsibilities: 
  • 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 organisational 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.

If this role is of interest to you, please apply now! 

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