Responsibilities:

• Provide expert consulting on GMP, GDP, or GCP compliance
• Support audits, gap assessments, and CAPA implementation
• Advise on quality systems and regulatory frameworks

Requirements:

• Proven experience in GxP environments
• Familiarity with EU and local pharma regulations
• Strong communication and report-writing skills

What’s on Offer:

• Flexible freelance or project-based work
• Opportunities to work with global clients
• Support impactful pharmaceutical development in emerging markets