Regulatory Affairs Specialist

20 hours ago


Irvine, California, United States Orion Group Full time
Job Summary

Orion Group is seeking a highly skilled Regulatory Affairs Specialist to support the development and implementation of the global regulatory strategy for company cosmetic and OTC products.

The ideal candidate will have a strong understanding of personal care product industry regulatory affairs discipline throughout the product lifecycle, including development, commercialization, and operations.

  • Review and prepare regulatory documents and labeling for cosmetic or OTC product registrations/updates.
  • Research and interpret health authority regulations/guidance and provide regulatory information to cross-functional teams.
  • Conduct regulatory assessments of product changes, labeling revision, and new product introduction.
  • Generate ingredient lists, quantitative and qualitative assessments, and cosmetic or OTC formulation assessments.

Key Responsibilities:

  • Review product labeling for accuracy and communicate planned/approved changes with other functions.
  • Provide regulatory guidance to other departments to ensure compliance with regulations.
  • Conduct regulatory assessments of product changes and labeling revision.
  • Generate regulatory documentation for cosmetic registration and respond to regulatory questions as needed.

Requirements:

  • BS degree in a scientific field, plus two years' experience in regulatory affairs; or equivalent relevant work experience.
  • MS degree in a scientific field, plus one year experience in regulatory affairs; or equivalent relevant work experience.
  • PhD degree in a scientific field, with no experience in regulatory affairs.


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