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Quality Assurance Specialist m/f/d

Aristo Group · Visp

Visp · On-siteFull-TimePosted Jun 24, 2026

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Job description

The Deviation Specialist will support a large-scale mammalian cell culture facility by owning and investigating deviations to ensure compliance, product quality, and continuous improvement.

Project title: Deviation Specialist (m/f/d)

Type of employment: Payroll

Industry: Engineering

Skills: Deviation management,Mammalian Genetics

Project start: 01.07.2026

Project duration: 6 months

Location: 3930 Visp, Switzerland

Tasks:

  • Own, document, and investigate deviations in alignment with cGMP requirements.
  • Collaborate with SMEs and stakeholders to determine root causes and assess product/system impact.
  • Apply structured investigational tools (e.g., Fishbone, Fault Tree, Event & Causal Factors).
  • Define effective CAPAs and associated effectiveness checks.
  • Drive timely closure of quality records and support process improvement initiatives.

Qualifications:

  • Bachelor’s degree in chemistry, biotechnology, life sciences, or related field.
  • Experience with deviations and cGMP in pharma/API is a strong advantage.
  • Knowledge of biotech manufacturing processes and analytical methods is beneficial.
  • Familiarity with Human & Organizational Performance and risk management is a plus.
  • Strong technical writing and communication skills; fluency in English (German is a plus).
  • Structured, organized, proactive, and open to change.

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