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Senior Manager, Quality Assurance & Regulatory

Job in El Segundo, Los Angeles County, California, 90245, USA
Listing for: Meaningful Beauty
Full Time position
Listed on 2026-03-01
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Meaningful Beauty is seeking a disciplined, detail oriented, and business minded Senior Manager, Quality Assurance and Regulatory to oversee product integrity and compliance across our portfolio of skincare, haircare, bodycare, and select OTC sunscreen products.

Founded by Cindy Crawford over 20 years ago, Meaningful Beauty delivers effective skincare solutions rooted in science and long‑term use to women 34+.

As Meaningful Beauty continues to expand its portfolio and increase product complexity, this role will ensure that quality systems, documentation, and regulatory processes are structured and aligned with the needs of a business at our scale and prepared for continued category growth. Reporting directly to the Co‑President, this individual will serve as the internal owner of quality documentation, compliance governance, and release readiness oversight.

This is a hands‑on individual contributor role requiring strong judgment, structured thinking, and the ability to collaborate effectively across functions.

Why This Role Matters

As Meaningful Beauty continues to evolve and expand its portfolio, the strength of its quality systems and compliance infrastructure must match the size and complexity of the brand. This role strengthens the brand’s ability to:

  • Maintain structured, audit‑ready documentation
  • Assess risk thoughtfully and proportionately
  • Reduce post‑launch compliance issues
  • Protect brand integrity while enabling innovation
What You Will Do Quality Systems & Documentation Ownership
  • Own and maintain PLM as the system of record for: formula documentation, packaging documentation, finished good specifications, COAs and SDSs.
  • Review production documentation and quality records prior to release readiness.
  • Develop, implement, and maintain SOPs governing documentation, change control, and compliance processes.
  • Lead investigations related to deviations, quality issues, and corrective actions.
  • Maintain product retains and quality standards.
  • Monitor complaint trends and ensure appropriate documentation and follow up.
  • Ensure documentation is structured, complete, and audit ready.
Regulatory Oversight
  • Manage product registrations and required filings across applicable regulatory bodies.
  • Ensure compliance with FDA cosmetic regulations and applicable OTC monograph requirements, including sunscreen labeling and Drug Facts panel standards.
  • Review formula and labeling documentation to ensure compliance prior to launch.
  • Maintain current raw material and supplier regulatory documentation.
  • Oversee adverse event documentation and required reporting.
  • Partner with Legal and cross‑functional teams on claims and labeling considerations.
Cross‑Functional Partnership
  • Collaborate closely with Sourcing & Operations, Packaging Engineering, and R&D to ensure alignment between innovation, manufacturability, and compliance.
  • Provide practical, proportionate risk assessment during development and production.
  • Elevate significant compliance or quality concerns to leadership when appropriate.
  • Support the business in minimizing late‑stage production surprises and post‑launch compliance issues.
Who You Are

The ideal candidate will be a detail‑oriented expert in quality assurance and regulatory compliance within the beauty or personal care industry who is able to work collaboratively with cross‑functional teams to ensure product integrity and compliance across Meaningful Beauty’s portfolio of products.

  • 8+ years of experience in quality assurance and/or regulatory within beauty or personal care.
  • Strong working knowledge of FDA cosmetic regulations.
  • Exposure to OTC products (sunscreen experience preferred but not required to be the primary focus).
  • Experience working with contract manufacturers.
  • Highly detail‑oriented with strong documentation discipline.
  • Experience reviewing COAs, batch documentation, and managing deviations.
  • Familiarity with adverse event documentation processes.
  • Sound business judgment with the ability to balance compliance rigor and operational practicality.
  • Collaborative communication style and comfortable working cross‑functionally.
  • Comfortable operating as an independent senior individual contributor in an established organization.
About Us

Mea…

Position Requirements
10+ Years work experience
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