description du poste

Senior Quality Assurance Auditor

I'm currently looking to speak with a highly experienced Quality Assurance Consultant to support a GMP Audit.

This is a short-term, on-site consulting engagement in Belgium, ideal for a senior QA professional who has led or conducted multiple inspections or mock inspections and is comfortable operating at an executive and inspection-facing level.

Key Details:

• 10+ years of Clinical QA / GMP experience
• Proven track record with FDA/EMA-style inspections or mock inspections
• 8 hours prep + 8 hours post-inspection report write-up
• Strong biotech/pharma clinical development background

Scope includes:

• GMP inspection readiness assessment
• Stakeholder interviews & document review
• Identification of inspection risks and gaps
• Clear, actionable mock inspection report

If you are a senior GMP QA consultant (or can recommend one) who enjoys high-impact, inspection-focused work, I'd love to connect.

Please message me directly or comment below.

#ClinicalQA #GMP #MockInspection #InspectionReadiness #ClinicalResearch #BiotechConsulting #QualityAssurance #FDA #EMA #ConsultingRoles