GxP Compliance & QA Auditor + SOP Writer (Hybrid)

PPG US ProPharma Group, LLC; West Virginia; Hybrid; USD 90,000 - 130,000; Full time

Job summary

ProPharma 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.

Qualifications

• Bachelor’s degree in a scientific discipline is required.
• Minimum 5 years in quality assurance and GxP compliance.
• Experience auditing and CAPA implementation.

Responsibilities

• Represent the company in QA and GxP projects.
• Provide consulting and project management support.
• Lead or participate in audits and CAPA activities.
• Promote quality systems and SOP training.

Skills

GxP knowledge

Regulatory compliance

Audit management

Client communication

Education

Bachelor’s degree in a scientific discipline

Graduate degree preferred

Tools

QMS knowledge

Job description

ProPharma 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.