Quality Assurance Expert

Location: Neuchâtel

Workload: 100%

Start: ASAP

Duration: Until 21/11/2025 with chances for extension

As a QA Expert, you’ll report directly to the QA Manager and ensure compliance, validation, and quality oversight across engineering and QC laboratory projects. You’ll be both the quality representative for day-to-day GMP activities and for major project-related deliverables.

• Reviewing and evaluating change requests per GMP requirements and internal procedures
• Acting as the Quality partner for QC Laboratory projects and facility projects
• Ensuring deployment and adherence to quality systems in line with regulatory expectations
• Overseeing quality aspects during validation (plans, protocols, URS, risk assessments, etc.)
• Leading or reviewing deviations and defining CAPAs using tools like TrackWise
• Proactively communicating project activities, findings, and risks
• Preparing and approving revisions of controlled documentation
• Reporting critical issues to functional and senior management

• Bachelor’s or Master’s degree in Engineering, Biotechnology, Pharmacy or Quality Management
• 3–5 years of experience in a GMP environment (preferably biotech/pharma)
• Solid knowledge of FDA, EMA, ICH, ISO standards, and data integrity principles
• Experience with QC equipment, CSV, and validation processes
• Affinity for digital tools and automated systems
• Excellent communication skills in French and strong English (spoken and written)
• Organized, proactive, pragmatic, and solution-oriented
• Comfortable working cross-functionally and in a fast-paced setting

• A long-term contract with strong potential for extension
• The chance to work on high-impact projects in a world-class biotech environment
• Supportive recruitment process and guidance from our team throughout