Joint skills in QA and IT required! French speaking job

• Join a Global Leader in Biopharmaceutical Innovation
• ASAP | Initial Contract: 6 months (extension highly probable until end of 2025)
• As a QA IT MES Specialist, you will be at the forefront of ensuring excellence and compliance during the implementation of an electronic batch record system. With a strong focus on Computerized System Validation (CSV), you will work alongside cross-functional teams to uphold the highest standards of quality and compliance.

What You’ll Do:

• Represent Quality in site and global project teams, providing oversight and expertise on CSV and validation activities.
• Ensure all quality aspects of the project comply with Global Policies, SOPs, and GMP regulations.
• Review and approve key documentation, including risk assessments, validation protocols, and configuration specifications.
• Collaborate with project teams to address quality issues, organize QA activities, and promote compliance with data integrity standards.
• Act as a key QA liaison, ensuring seamless communication among stakeholders and supporting an agile validation approach.

What You’ll Bring:

• Proven experience in Computerized System Validation (CSV) and a strong understanding of cGxPs and industry standards.
• Fluency in English and French is essential.
• Exceptional communication and organizational skills to collaborate across diverse teams.
• A proactive mindset with the flexibility and dedication to meet project timelines.
• Residency or work permit in Switzerland is mandatory (cross-border workers welcome).

What’s in it for You?

• Be part of a globally renowned biopharmaceutical company.
• Collaborate on cutting-edge projects that shape the future of healthcare.
• Work in a state-of-the-art facility overlooking the beautiful Lake of Neuchâtel.