Hybrid Director, Regulatory Affairs

Posted 6 hours ago

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About the role

  • Director of Regulatory Affairs managing compliance for Luxury Brand Partners in beauty industry. Collaborating with product development and marketing teams while ensuring regulatory standards are met.

Responsibilities

  • Act as subject matter expert on regulatory affairs, safety and quality assurance.
  • Manage the regulatory department and oversee the day-to-day work of all regulatory associates.
  • Understand and manage formula and packaging compliance with US (e.g. California labeling guidelines) and international regulations for new and existing products.
  • Stay up to date with regulatory changes impacting ingredients and products and communicate developments to management and suppliers.
  • Ensure all products are in compliance with domestic and international regulatory, environmental and hazmat shipping regulations.
  • Author & maintain Safety Data Sheets, NAFTA certificates, handle regulatory filings and necessary updates to regulatory filings in each market (e.g., US, Canada, Europe).
  • Manage FDA registrations to ensure company compliance with new MOCRA regulations.
  • Ensure compliance with California Air Resource Board.
  • Support PD with performing product name trademark searches and compliant product descriptions based on global market requirements.
  • Support PD and marketing in clinical and consumer product claims testing.
  • Work closely with PD to evaluate product and packaging copy and providing feedback and recommended verbiage to ensure claims and verbiage are legal and substantiated.
  • Risk-assess every product launch (ie formula, product copy, claims, packaging labeling, marketing claims, etc) and call-out any potential concerns.
  • Generate ingredient lists for labeling of all products.
  • Perform artwork/label review from both a technical and claims perspective. Final approval of primary and secondary copy.
  • Address all product and regulatory questions from the team.
  • Approval of all product claims and consumer-facing marketing copy.
  • Perform all OTC evaluations and provide guidance to the team on process and requirements, including development, testing, labeling, copy/claims, FDA registration, launch, complaints, etc.
  • Compile documentation and maintain European regulatory Product Information Files for each product.
  • Oversee processes and advise on entering new markets from a regulatory standpoint.
  • Recommend and oversee quality assurance programs.
  • Oversee product safety, stability and claims testing (Micro, safety, RIPT).
  • Advocate for the company with industry associations and represent Luxury Brand Partners and its brands in industry groups (e.g., ICMAD, PCPC).
  • Act as primary point of contact and liaison for internal teams, vendors and regulatory representatives, MOH, etc.
  • Advise on ingredient usage, from a regulatory and marketing perspective for new formulation.
  • Create new operating procedures and protocols and create standardized written policies.
  • Proactively educate the team on ongoing or potential new regulations that may be passed into law; most importantly for the PD team to initiate reformulations and/or revisions with packaging and labeling.

Requirements

  • 10+ years of industry experience in regulatory affairs
  • Beauty, Skin Care, Hair Care and/or CPG experience a plus
  • Master’s degree in scientific discipline such as chemistry, biology, toxicology or environmental science is a plus
  • Expert understanding of global cosmetic and chemical regulations
  • Extensive knowledge of safety regulations and industry standards relating to a variety of consumer products in the US, EU and Canada
  • Product development experience is a plus
  • OTC experience is a plus
  • Established industry relationships
  • Excellent verbal & written communication and organizational skills
  • Extremely detail-oriented
  • Strategic thinker who blends strong analytics and creativity and curiosity
  • Strong work ethic and can-do attitude
  • Problem solving and entrepreneurial in nature
  • Ability to manage multiple projects and priorities simultaneously
  • Strong team player
  • Thrive in a fast-paced entrepreneurial environment

Benefits

  • Comprehensive health, dental, and vision insurance along with additional ancillary benefits
  • Flexible spending and health savings accounts (FSA/HSA)
  • Employer paid life insurance coverage with optional supplemental life insurance available
  • Employer paid long-term and short-term disability
  • Access to Employee Assistance Program (EAP)
  • Starting with 10 vacation days, 4 fixed personal days and 5 sick days (unless state law requires otherwise, in which case we will comply with state law)
  • Twelve paid holidays
  • Paid parental leave
  • Summer Fridays between Memorial Day & Labor Day
  • Compensation commensurate with industry standards and your qualifications
  • 401(k) with company match
  • Monthly technology allowance
  • Eligible for annual discretionary bonus

Job title

Director, Regulatory Affairs

Job type

Experience level

Lead

Salary

$150,000 - $170,000 per year

Degree requirement

Postgraduate Degree

Location requirements

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