Posted:
February 18, 2026
Location:
Visp, Valais, Switzerland

Job Description

Key Responsibilities

  • Take ownership of deviation records from initiation through investigation to final closure
  • Lead root cause investigations and document findings in compliance with internal quality standards
  • Partner with Subject Matter Experts and relevant stakeholders to evaluate deviation impact on products and systems
  • Apply structured investigational methodologies such as Fault Tree Analysis, Fishbone Diagram or Event and Causal Factor Analysis
  • Define appropriate CAPAs and effectiveness checks to ensure sustainable resolution and prevent recurrence
  • Maintain full compliance with cGMP requirements throughout the investigation lifecycle
  • Ensure accurate documentation and timely completion of quality records
  • Contribute to continuous improvement initiatives and support ongoing operational changes

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Job Overview

Job Type: Full-time
Location: Visp, Switzerland
Posted: February 18, 2026
Deadline: March 30, 2026