Project details
Recommended projects
Quality Compliance Auditor (GCP/GCLP/GVP) (M/W/D)
Senior Regulatory Compliance Expert (FDA inspection preparation) (m/f/d)
EHS Specialist – Cell Manufacturing
EHS Specialist – Facilities (M/W/D)
EHS Specialist – Body in White (M/W/D)
Cyber Risk Consulting (Senior Level)
AI Evaluation Consultant (m/w/d)
Tax Strategy Consulting
Construction & Contractor Safety Specialist (SiGeKo) (M/W/D)
Cyber Security Consultant – Product Security & Regulatory Compliance (m/f/d)
Commissioning & Qualification (C&Q) Engineer (m/f/d)
Senior Factor 10 Developer (IPS / IPM) (m/f/d)
Dentist for Training AI Models (m/f/d)
Biologist with Python Experience (m/w/d)
Project Manager/Account Manager (Senior to Director) (m/f/d)
Project Manager Brand Guardianship (m/f/d)
Freelance Electrical Engineer with Python Experience (m/w/d)
Project Manager for Magazines / Magazine Production (m/f/d)
Sales Manager for a Media Company (m/f/d)
IT project manager ISO 27001 - Gap Closure (m/f/d)
Freelance Automotive Engineer (with Python) - Quality Assurance / AI Trainer
Freelance Biology Expert for AI Model Training (m/f/d)
Safety and Health Protection Coordinator (SiGeKo) and Safety Specialist (SiFa) (m/f/d)
Account Manager B2B for a Media Company (m/f/d)
Senior Project Manager Customer Interaction
ERP Transformation Manager (m/f/d)
IT Project Manager ServiceNow (Senior)
Freelance Product Owner for Point of Sale App
Control Systems Technician / Control Systems Specialist (m/f/d)
Development of TM1 Planning Analytics and Interfaces (m/f/d)
Java IT Architect (m/f/d)
Frontend developer to HR platform with Angular experience
Quality Compliance Auditor (GCP/GCLP/GVP) (M/W/D)
Project info
- Period09.02.2026 - 14.06.2026
- Capacityfrom 95%
- LocationGermany
- Languages
- German(Advanced),
- English(Advanced)
- German
- Remoteup to 100%
Description
A company is looking for an experienced Quality Compliance Auditor responsible for ensuring compliance with GCP, GCLP, and GVP standards. The project's aim is to conduct internal and external audits, prepare and support regulatory inspections, and identify compliance gaps to derive corrective actions.
The role includes planning and conducting audits, supporting regulatory inspections, and ensuring compliance with ICH guidelines as well as EMA/FDA regulations.
- Conduct internal and external audits (GCP, GCLP, GVP)
- Prepare and support regulatory inspections (e.g., MHRA, FDA, EMA)
- Identify compliance gaps and derive corrective actions
Requirements
- Master's degree in life sciences, pharmacy, medicine, or quality management
- 5–10 years of professional experience in clinical research, pharmacovigilance, or laboratory compliance
- Hands-on experience with ICH guidelines and EMA/FDA regulations
- Proven experience in audit planning and CAPA management
- Understanding of clinical trial processes and documentation
- Knowledge of pharmacovigilance systems and data integrity
- Strong communication and reporting skills
- Certification (e.g., RQA) preferred
- Experience with risk-based audit approaches