• New York, NY
  • $43–$55 Per Hour
  • Quick Apply
4 days ago

Job Description

Summary:
  • The Regulatory Affairs Manager ensures regulatory compliance of The Avon/LG H&H US cosmetic, OTC, dietary supplement, and device products from brief through launch in North America. Specifically, the Manager will assemble and review all product-related information including formulas, specifications, and quality/regulatory compliance documentation, and for approving claims, labeling, and advertising.
  • Communicate emerging regulations to key stakeholders and their impact on The Avon/ LG H&H US portfolio in NA.
  • This is a 6 months contract to hire role.
  • You will report to the Senior Manager, Quality, Safety and Regulatory Affairs.
Roles & Responsibilities:
  • Participate in project teams in assigned categories to ensure completion of appropriate documents during the development process through final formula approval and launch.
  • Maintain and ensure compliance with The Avon ingredient policies and appropriate product regulations.
  • Ensure claims are compliant with The Avon and local regulatory requirements and consistent across labels, advertising, and other consumer communications.
  • Review and approve NA artworks.
  • Responsible for US regulatory submissions, including FDA drug and establishment registrations, supplement notifications, WERCS and EPA and state pesticide registrations.
  • Assist monitoring US state and federal regulations impacting the cosmetic and personal care industry including OTC.
  • Support with upcoming changes in the regulations including any specific monitoring and implementation for states, e.g., California.
Minimum Qualifications:
  • Scientific degree.
  • Over 5 years of Regulatory Affairs experience within a regulated industry, preferably skin and personal care products including OTC.
  • Product development experience strongly preferred.
  • Skin and personal care including OTC claim review experience strongly preferred.
  • Track record adhering to compliance requirements (i.e. FDA, Health Canada, EPA, FTC, cGMP, ISO, etc.).
  • Strong written communication skills, especially detail oriented and technical material.
  • Experience communicating with cross-functional teams and customers including verbal presentations.
  • Ability to work effectively both independently and as part of a team.
  • Ability to meet deadlines while being flexible to changes in priorities and interruptions.
  • Excellent organizational and analytical skills to complete assignments accurately.
  • Full usability of MS Office suite (Excel, Word, Outlook, PowerPoint).

Numbers & Facts

LocationNew York, NY
Salary$43–$55 Per Hour

Skills

  • Advertisingunmatched
  • Analysis Skillsunmatched
  • Communication Skillsunmatched
  • Consultingunmatched
  • Consumer Advertisingunmatched
  • Cross-Functionalunmatched
  • Current Good Manufacturing Practice (cGMP)unmatched
  • Detail Orientedunmatched
  • Documentationunmatched
  • Environmental Protection Agency (EPA)unmatched
  • FDA (Food and Drug Administration)unmatched
  • Federal Laws and Regulationsunmatched
  • Health Canadaunmatched
  • ISO (International Organization for Standardization)unmatched
  • Maintain Complianceunmatched
  • Microsoft Excelunmatched
  • Microsoft Officeunmatched
  • Microsoft Outlookunmatched
  • Microsoft PowerPointunmatched
  • Microsoft Wordunmatched
  • Organizational Skillsunmatched
  • Personal Careunmatched
  • Product Developmentunmatched
  • Product Reviewsunmatched
  • Regulationsunmatched
  • Regulatory Complianceunmatched
  • Regulatory Requirementsunmatched
  • Safety/Work Safetyunmatched
  • Sales Presentationunmatched
  • Skin Careunmatched
  • State Laws and Regulationsunmatched
  • Time Managementunmatched
  • Usability Engineeringunmatched
  • Writing Skillsunmatched

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