Validation Engineer

Innovative Skincare-posted 25 days ago
Full-time • Mid Level
Onsite • Mesa, AZ
101-250 employees
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The Validation Engineer is responsible for developing, executing, and documenting validation protocols to ensure equipment, systems, and processes meet regulatory and company requirements. This role supports GMP compliance by validating new and existing equipment, utilities, and manufacturing processes. This position will be on-site in our new Mesa, AZ facility.

  • Develop and execute validation protocols (IQ, OQ, PQ) for equipment, utilities, and processes.
  • Prepare and maintain validation documentation, reports, and records.
  • Ensure compliance with GMP, SOPs, and regulatory guidelines.
  • Support commissioning and qualification of new equipment and systems.
  • Investigate and resolve validation deviations or non-conformances.
  • Work with Quality, Engineering, and Production teams to implement validated systems.
  • Participate in risk assessments and change control activities.
  • Support audits, inspections, and continuous improvement in validation practices.
  • Train staff on validation procedures when required.
  • Bachelor’s degree in Engineering, Life Sciences, or related field required.
  • 2+ years of experience in validation, quality, or engineering in a GMP-regulated industry.
  • Strong knowledge of validation principles, protocols, and regulatory standards (FDA, cGMP, ISO).
  • Strong organizational, analytical, and documentation skills.
  • Good communication and cross-functional teamwork abilities.
  • Must be able to lift up to 40 lbs and work in lab, production, and utility environments.
  • Must be able to stand and walk for extended periods of time
  • Must be able to sit and use a computer for long periods of time
  • Experience with equipment qualification and process validation preferred.
  • 401k
  • Life
  • Dental
  • Vision
  • Health
  • PTO
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