1 year contract – hybrid Job Model – French speaking desired

Are you passionate about bridging IT and Quality in a highly regulated environment? We are looking for an experienced Life Science professional to take on a pivotal role ensuring IT compliance and quality oversight across complex manufacturing systems.

What you’ll do

• Act as the key contact between IT and Quality, fostering a strong quality culture.
• Ensure compliance of site IT systems with GxP, EU-GMP Annex 11, and 21 CFR Part 11.
• Lead Computer System Validation (CSV) activities and support data integrity programs.
• Translate compliance requirements into test strategies (FAT, SAT, IQ, OQ, PQ).
• Partner with cross-functional teams and external stakeholders to drive compliance and continuous improvement.
• Support audits, infrastructure integration, and remediation projects.

What you bring

• A degree in Life Sciences, Quality, Engineering, or related field.
• 5–10 years of experience in the pharmaceutical, biotech, or life science industry, with at least 5 years in IT compliance, validation, or quality roles.
• Solid knowledge of Quality Management Systems, GxP systems (MES, LIMS, etc.), and Data Integrity.
• Strong IT foundation (OS, infrastructure, networking, systems).
• Expertise in CSV and regulatory frameworks (21 CFR Part 11, EudraLex, MHRA).
• Excellent communication skills, a structured and analytical mindset, and the ability to thrive in an international, multidisciplinary environment.

Why join?
This is a unique opportunity to contribute to high-impact manufacturing operations, ensuring compliance, data integrity, and patient safety. You’ll work in a dynamic environment that values ethics, collaboration, and continuous learning.