2-Month Contract (m/f/d)Start: 01 Sept 2025 | home office 1 day after onboarding

Are you ready to take ownership in a highly regulated and innovative environment? In this role, you will ensure quality oversight and compliance of all IT systems at the manufacturing site in Boudry. You will collaborate closely with internal teams and external partners to ensure all systems meet regulatory requirements (including EU-GMP Annex 11 and 21-CFR Part 11) and uphold the highest quality standards.

Key Responsibilities:

• Ensure quality and compliance for site IT systems
• Implement and monitor regulatory requirements
• Support audits and data integrity initiatives
• Act as a bridge between IT, Quality Assurance, and business functions
• Lead and facilitate meetings on IT compliance topics

Your Profile:

• University degree in IT, Quality, Engineering, or related field
• Minimum 5 years in a similar role within the pharmaceutical/biotech industry
• Strong knowledge of GxP systems and Computer System Validation (CSV)
• In-depth understanding of 21-CFR Part 11, EU-GMP, and Data Integrity requirements
• Fluent in English; French is a plus
• Analytical, structured, and solution-oriented mindset

Special Requirements:

• Full-time on-site presence (home office possible up to 1 day/week after onboarding)
• Applicants must be based in Switzerland or hold a valid Swiss work permit