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Alexis Lambert

Regulatory Affairs and Document Control Specialist

Talent
Fairbanks, AlaskaMember since July 17, 2026
Regulatory AffairsDocument ControlChange ControlHealth CanadaRegulatory DocumentationQuality SystemsCross-Functional Collaboration
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Regulatory AffairsDocument ControlChange ControlHealth CanadaRegulatory Documentation

About

Regulatory Affairs and Document Control Specialist with 5+ years of experience supporting regulatory compliance, quality systems, and product development in the dietary supplement and cosmetics industries. Experienced in change control, regulatory documentation, product labeling, and cross-functional collaboration.

Experience

Document Control Specialist - doTERRA

(2023-12 - 2024-05)

  • Managed end-to-end change control processes, ensuring changes were evaluated, approved, and documented in compliance with quality standards.
  • Conducted impact assessments and coordinated implementation plans with cross-functional stakeholders.
  • Maintained change control documentation and reports to support audits and post-implementation reviews.

Regulatory Document Control Specialist - LifeVantage

(2022-11 - 2023-10)

  • Built and managed a centralized raw material document library, improving accessibility and regulatory compliance.
  • Developed raw material specifications and collaborated with suppliers and internal teams to support product development.
  • Reviewed regulatory documentation and implemented pre-launch product checklists for domestic and international markets.

Regulatory Affairs Specialist - Xyngular

(2021-05 - 2022-09)

  • Reviewed product labels and claims for regulatory compliance across U.S. and international markets.
  • Supported international product registrations and Health Canada NPN compliance.
  • Maintained regulatory documentation and developed standardized labeling guidelines.

Document Control Specialist - Modere

(2019-09 - 2021-05)

  • Created and audited master batch records to support compliant manufacturing operations.
  • Investigated product complaints and adverse events, supporting FDA and Health Canada reporting requirements.
  • Reviewed manufacturing documentation to ensure quality and regulatory compliance.

Education

High School Diploma - Spanish Fork High School

Skills

Regulatory Affairs and Document Control Specialist

Reviews

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