QA Expert (Senior)

QA Expert (m/f/d)

Location: Neuchâtel, Switzerland
Duration: 01/05/2026 to 30/09/2026

Responsibilities

• Act as Quality Assurance representative for routine GMP activities and site improvement projects related to bulk drug substance (BDS) manufacturing and release.
• Ensure compliance with current GMP guidelines, regulatory requirements and internal quality standards throughout manufacturing and release processes.
• Perform inspection and release of raw materials and externally manufactured BDS.
• Ensure release planning is up to date and contribute to KPIs related to raw material release.
• Ensure proper archiving of quality documentation in accordance with applicable requirements.
• Prepare, evaluate, review and approve new or revised controlled documents (e.g. SOPs, procedures, forms, specifications, quality systems documentation).
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