GxP Compliance & QA Auditor + SOP Writer; Hybrid
Listed on 2026-11-01
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Quality Assurance - QA/QC
Regulatory Compliance Specialist -
Pharmaceutical
Regulatory Compliance Specialist
Pro Pharma is seeking a Compliance and Quality Assurance Consultant (CQA) to support management of compliance and quality assurance projects across GxP domains, including GMP, GCP, and GLP. The role involves client-facing consulting, QA oversight, audits, and development of QMS.
You will work with cross-functional teams, stay current with FDA/EMA regulations, travel as needed, and contribute to CAPA implementation while promoting continuous improvement.
This is an excellent opportunity to take on the GxP Compliance & QA Auditor + SOP Writer (Hybrid) role at PPG US Pro Pharma Group, LLC.
We appreciate your interest in this position.
Join PPG US Pro Pharma Group, LLC and contribute to our ongoing work.
Take a moment to read everything above and see whether this role is right for you.
This posting is for the GxP Compliance & QA Auditor + SOP Writer (Hybrid) role at PPG US Pro Pharma Group, LLC, based in WV, United States.
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