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Scientist, Validation & Investigations - French speaking

Job in 6300, Zug, Kanton Zug, Switzerland
Listing for: AurigaVision AG
Contract position
Listed on 2026-06-06
Job specializations:
  • Engineering
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 30000 - 80000 CHF Yearly CHF 30000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Scientist, Validation & Investigations  - French speaking | 6 month duration

Our client is a science-driven pharmaceutical organization focused on developing and ensuring robust manufacturing processes across the full product lifecycle. For a manufacturing site in Switzerland, we are currently looking for a

Scientist, Validation & Investigations ()
French speaking | 6 month duration

In this role you will support validation and investigation activities within manufacturing processes, contributing to product quality and compliance. The position involves close collaboration with cross-functional teams, including Engineering, Technical Services, Manufacturing, Quality Control, and Quality Assurance. In addition, the role requires interaction with global MS&T teams and participation in continuous improvement initiatives.

Your main tasks
  • Prepare and maintain validation and qualification documentation, including protocols, reports, and traceability matrices
  • Execute validation, qualification, and robustness activities, including data collection and analysis
  • Support the implementation of new products, technologies, and systems at the manufacturing site
  • Assess the impact of changes, deviations, and maintenance interventions on validated systems
  • Conduct and lead investigations, including root cause analysis and implementation of corrective and preventive actions
  • Perform scientific risk assessments and contribute to deviation classification processes
  • Participate in audits, inspections, and continuous improvement activities within MS&T projects
Your profile
  • Degree in Engineering, Chemistry, Pharmacy, or a related natural science field
  • Fluency in French & English
  • Professional experience in pharmaceutical operations, validation, or quality-related functions (MS&T)
  • Solid understanding of current regulatory requirements and GxP standards
  • Strong analytical and problem-solving skills
  • Ability to work across functions and communicate effectively at different organizational levels
  • Experience in health authority inspections or audit support is considered a plus
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