We are looking for a consultant to support validation activities in IT projects within the Life Sciences industry. The role focuses on documentation, testing, and ensuring that IT systems meet internal quality and regulatory requirements. You will work as part of a project team and receive guidance from senior consultants and project managers.

Key Responsibilities

• Support IT projects with documentation and testing tasks
• Participate in system testing (IQ, OQ, PQ, UAT support)
• Help review documents to ensure compliance with company procedures
• Support risk assessments and deviation documentation
• Collaborate with project team members and stakeholders

Qualifications

• 0–2 years of experience in IT, validation, or regulated environments
• Fluent in French OR German language (spoken, written, reading, and listening)
• French: with an official certificate such as DELF/DALF (B2/C1...