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Regulatory Compliance Coordinator

Contract type

Location

Marina del Rey, CA

Specialty

Salary

$30/hour - $35/hour

Remote

Yes

Reference

516929

Contact name

Lexy Hartwell

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Job description

We are seeking a detail-oriented Regulatory Compliance Coordinator to join a personal care brand! This role will manage day-to-day administrative regulatory workflows, including document procurement, product testing logistics, product registrations, and Toxicological Risk Assessment (TRA) initiation.

Details:

  • Hourly rate: $30-35/hr. DOE
  • Schedule: 30-40 hours a week
  • Duration of assignment: 6-month contract
  • Location: Marina del Rey, CA 90292
  • Schedule: Hybrid

Key Responsibilities

  • Request, gather, and organize compliance documentation from raw material manufacturers, testing facilities, and internal sources (e.g., laboratories, Qualio, artwork folders).
  • Conduct preliminary reviews of raw material documents against internal brand standards and regional regulatory requirements.
  • Maintain clean, centralized, and up-to-date filing systems and follow up with external suppliers to retrieve missing information.
  • Coordinate and oversee sample procurement, preparation, packaging, and shipping for product testing (including WERCS testing).
  • Track testing progress with external laboratories and follow up to ensure timely delivery of results.
  • Maintain logs and file completed lab reports in designated system folders.
  • Prepare and submit product registrations across required portals, including MoCRA, CDPH (performing basic fragrance allergen calculations), and WERCS.
  • Track registration statuses and maintain accurate records of all submissions and approvals.
  • Gather initial formulas, safety data sheets (SDSs), supplier documentation, and required inputs to initiate ad-hoc TRA requests for senior toxicologists/reviewers.

Qualifications & Skills

  • 1–3 years of experience in regulatory compliance, quality administration, supply chain, or a related technical support role (experience in cosmetics, personal care, or CPG preferred).
  • Familiarity with FDA/MoCRA, CDPH, WERCS, or raw material safety documentation (SDSs, COAs, allergen declarations) is a strong plus.
  • Basic proficiency in performing calculations (e.g., fragrance allergen percentages).
  • Familiarity with Quality Management Systems (e.g., Qualio), document control systems, and MS Office / Google Workspace.
  • Exceptional attention to detail and organizational skills.
  • Strong written and verbal communication skills for supplier follow-ups and internal cross-functional collaboration.
  • Ability to manage multiple priorities in a fast-paced environment and track recurring tasks to completion.

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