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Regulatory Affairs Specialist

4 months ago

United Kingdom Meet Recruitment Limited Full time

I am seeking a highly motivated and experienced Regulatory Affairs Specialist with expertise within OTC/Cosmetics experience to join us on a contracted basis for a period of 6 to 12 months. As a key member of the Regulatory Affairs team, you will play a crucial role in ensuring our products comply with all relevant regulations and standards in various markets.

Responsibilities:

  • Conduct regulatory assessments and ensure compliance of cosmetic products with local and international regulations, including but not limited to FDA, EU, and other global regulatory agencies.
  • Prepare and submit regulatory documents, including ingredient lists, safety assessments, and product dossiers, for product registrations and approvals.
  • Stay up-to-date with changes in regulations and guidelines affecting the cosmetics industry and provide guidance to internal teams on compliance requirements.
  • Collaborate cross-functionally with R&D, Quality Assurance, Marketing, and other departments to support product development and launch activities.
  • Respond to regulatory inquiries and requests for information from regulatory authorities in a timely and accurate manner.
  • Participate in regulatory audits and inspections, ensuring all documentation and processes meet regulatory requirements.

Qualifications:

  • Bachelor’s degree in a scientific discipline or related field; advanced degree preferred.
  • Minimum of 4-6 years of experience in regulatory affairs within the OTC/Cosmetics industry.
  • In-depth knowledge of cosmetic regulations and guidelines, including experience with FDA, EU Cosmetics Regulation, and other global regulatory frameworks.
  • Proven track record of successful product registrations and approvals in various markets.
  • Strong attention to detail and excellent analytical skills.
  • Ability to effectively communicate complex regulatory requirements to cross-functional teams.
  • Experience with regulatory submissions and documentation management systems is preferred.
  • Regulatory affairs certification or professional accreditation is a plus.
  • MUST be based in the UK

Contract Details:

  • Type: Contract, 6-12 months (with possibility of extension)
  • Location: Hybrid/Remote (Circumstances dependant)
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