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Quality Assurance Specialist

Valais
NOUVEAU
  • 07.10.2026
  • 100%
  • Poste à responsabilités
  • Temporaire

Quality Assurance Specialist

Location: Visp, Valais, Switzerland
Contract Duration: Minimum 6 months
Start Date: Immediate availability required
Industry: Pharmaceutical / Biotechnology
Languages: Fluent English and German (mandatory)
About the Role

We are currently seeking an experienced Quality Assurance Logistic Specialist - Raw Materials to join a leading pharmaceutical and biotechnology manufacturing environment in Visp, Valais. This is an excellent opportunity for a quality professional with a strong GMP background and proven experience in raw material qualification, supplier management, and material release activities.

The successful candidate will play a key role in ensuring the compliant receipt, qualification, release, and supplier management of raw materials while supporting GMP-compliant manufacturing operations.

Key Responsibilities
  • Perform incoming raw material verification in accordance with applicable GMP procedures and quality standards.
  • Manage the qualification and release of raw materials used in manufacturing processes, including physical verification and release activities within LIMS.
  • Establish, maintain, and monitor approved raw material suppliers, SOPs, and quality systems.
  • Review and manage supplier change notifications and quality alerts.
  • Investigate and manage material-related deviations, non-conformances, and change controls.
  • Monitor and collect KPIs associated with raw material qualification and release activities.
  • Ensure accurate and compliant documentation and data management.
  • Escalate critical quality issues and potential compliance risks in a timely manner.
  • Collaborate closely with Manufacturing, QC, Supply Chain, and external suppliers to ensure uninterrupted operations.
  • Support continuous improvement initiatives related to raw material management and supplier quality processes.
Required Qualifications
  • Bachelor's degree in Life Sciences, Chemistry, Biotechnology, Pharmacy, or a related scientific discipline.
  • Minimum 3 years of confirmed experience in Quality Assurance within the pharmaceutical or biotechnology industry.
  • Strong knowledge of GMP regulations and quality systems.
  • Experience with:
    • Raw material qualification and release
    • Supplier quality management
    • Deviations, CAPAs, and Change Controls
    • LIMS and electronic quality systems
    • Quality risk assessment
Language Requirements
  • English: Fluent (mandatory)
  • German: Fluent (mandatory)