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.
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