Jobs · Quality Assurance · California

Validation Coordinator

Actalent · Los Angeles, CA · 1 mo ago
On-siteQuality Assurance$22–$26/hrContract

Position Summary

The Sanitation Validation Coordinator is responsible for managing and maintaining sanitation validation documentation in support of manufacturing operations within a cosmetic contract manufacturing environment. This role partners closely with Quality, Manufacturing, Validation, and Sanitation teams to ensure validation records are accurate, compliant, and audit-ready.

Key Responsibilities

  • Cook up and maintain validation protocols, reports, forms, logbooks, and supporting records.
  • Prepare and route validation packets for accuracy, completeness, and compliance.
  • Ensure all required approvals, signatures, and supporting data are properly documented.
  • Track validation projects and schedules to support production timelines.
  • Collaborate with cross-functional teams to resolve documentation discrepancies.
  • Generate and maintain SOPs, work instructions, and validation templates.
  • Support investigations related to documentation errors, deviations, and validation exceptions.
  • Maintain organized, inspection-ready electronic and paper validation files.
  • Aid during customer audits, regulatory inspections, and internal audits.
  • Monitor validation status and communicate project updates to management.
  • Support continuous improvement initiatives and ensure compliance with cGMP requirements.

Qualifications

  • Education: Associate's or Bachelor's degree in Life Sciences, Chemistry, Biology, Quality, Engineering, or a related field preferred. Equivalent experience may be considered.
  • Experience: 1-3 years of experience in Quality Assurance, Document Control, Validation, Regulatory Affairs, or a GMP-regulated environment. Experience with validation protocols, batch records, and controlled documentation preferred. Cosmetics, personal care, pharmaceutical, food, or consumer products manufacturing experience is a plus.

Required Skills

  • GMP/cGMP compliance
  • Quality Assurance and Document Control
  • Validation documentation and packet review
  • SOP creation and revision
  • Good Documentation Practices (GDP)
  • Strong proofreading and attention to detail
  • Change control and record management
  • Microsoft Office (Excel, Word, Outlook)
  • Excellent organization and communication skills

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