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
Interested? We are looking forward to get in touch with you.
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