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Regulatory Manager

Job in Los Angeles, Los Angeles County, California, 90079, USA
Listing for: American International Industries
Full Time position
Listed on 2026-02-01
Job specializations:
  • Healthcare
    Healthcare Compliance
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Personal Care & Beauty Products | Onsite | Full-Time

A leading manufacturer and distributor of beauty and personal care products is seeking an experienced Regulatory Affairs Manager to join our team. This is a full-time, onsite role supporting domestic and international regulatory compliance across our product portfolio.

About the Role

In this role, you will be a key contributor to global product compliance, ensuring that all cosmetic and personal care products meet applicable regulatory requirements across multiple markets. You will partner cross-functionally with Quality, R&D, Product Development, and Commercial teams to support product launches, registrations, and ongoing compliance.

The ideal candidate is detail-oriented, proactive, and current on global cosmetic regulations, with the ability to translate regulatory requirements into practical business solutions.

Key Responsibilities
  • Prepare and manage global regulatory submissions, including registrations, renewals, amendments, and annual updates
  • Coordinate and compile documentation for international cosmetic regulatory filings
  • Obtain FDA Certificates of Export and other applicable export documentation
  • Monitor and interpret global regulatory changes impacting cosmetic and personal care products
  • Maintain organized and compliant regulatory files and archives in accordance with U.S. and international requirements
  • Develop and maintain a regulatory reference library, including company documentation and regulatory guidance
  • Advise internal teams on product registration strategies, market entry requirements, and ingredient compliance
  • Review and approve ingredient disclosures, quantitative/qualitative formulas, and label claims
  • Support Quality by creating and reviewing documentation such as Certificates of Analysis (COAs), specifications, and stability data
  • Prepare, revise, and manage Safety Data Sheets (SDS) in compliance with global standards
  • Support compliance activities related to CARB, VOC, EPA, and transportation regulations (DOT / IATA / IMDG)
  • Collaborate cross-functionally to ensure customer and regulatory satisfaction across assigned markets
  • Perform additional regulatory duties as required
Qualifications & Experience
  • Bachelor’s degree in Chemistry, Life Sciences, Engineering, or a related field (preferred)
  • 5–7+ years of Regulatory Affairs, Quality, or Product Development experience within cosmetic or personal care manufacturing
  • Associate/Specialist level candidates with 3–5 years of relevant regulatory experience will also be considered
  • Strong working knowledge of U.S. and international cosmetic regulations, including EU Cosmetic Regulation (EC) No. 1223/2009
  • Familiarity with CARB surveys, VOC regulations, and global compliance requirements
  • Understanding of manufacturing and quality systems
  • Experience preparing regulatory submissions and compliance documentation
  • Excellent written and verbal communication skills
  • Strong organizational skills with exceptional attention to detail
  • Ability to work independently and manage multiple priorities
  • Proficiency with Microsoft Office and regulatory documentation systems

Our benefits include medical, dental, vision, paid time off, holiday pay, supplemental insurance and voluntary life insurance.

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