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Regulatory Affairs Specialist

  1. East Anglia
Buckinghamshire
  1. Contract
Competitive
  1. Drug Safety / Pharmacovigilance
35688
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Regulatory Affairs Specialist - Pharmaceuticals - 12-Month Contract 

Our client has an exciting new opportunity for a Regulatory Affairs Specialist to join the team. Our client has specialised in pharmaceutical products and people's well-being for over a century and work with some well-known household brands. 


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 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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