Senior Manager Regulatory Affairs | $90,000- 140,000/Yr

PWR Staffing is collaborating with Crowdstaffing to hire a Senior Regulatory Affairs (RA) Manager for beauty client in New York, NY.

Job Overview:

The Senior 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 Sr. 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.

You will report to the Head of Sr. RA manager.

- Work Type: Full-time

- Work condition: Temporary Hybrid (3 days week in office)

Roles & Responsibilities

Specific Duties and Responsibilities

• Support with upcoming changes in the regulations including any specific monitoring and implementation for states, e.g., California
• Ensure claims are compliant with The Avon and local regulatory requirements and consistent across labels, advertising, and other consumer communications
• Participate in project teams in assigned categories to ensure completion of appropriate documents during the development process through final formula approval and launch
• Review and approve NA artworks
• Assist monitoring US state and federal regulations impacting the cosmetic and personal care industry including OTC
• Maintain and ensure compliance with The Avon ingredient policies and appropriate product regulations
• Responsible for US regulatory submissions, including FDA drug and establishment registrations, supplement notifications, WERCS and EPA and state pesticide registrations

Minimum Qualifications

Qualifications

• Over 8 years of Regulatory Affairs experience within a regulated industry, preferably skin and personal care products, including OTC
• Experience communicating with cross-functional teams and customers including verbal presentations
• Excellent organizational and analytical skills to complete assignments accurately
• Track record adhering to compliance requirements (i.e. FDA, Health Canada, EPA, FTC, cGMP, ISO, etc.)
• Product development experience is strongly preferred
• 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
• Scientific degree
• Full usability of MS Office suite (Excel, Word, Outlook, PowerPoint)
• Skin and personal care, including OTC claim review experience, strongly preferred
• Strong written communication skills, especially detail oriented and technical material