BAS Systems Administrator (100%)
Fehraltorf (Zurich), Switzerland
Job Posting Categories – Bioanalytical Services /
Full-Time /
Hybrid
At Celerion, we are driven by one mission: to advance clinical research and bring life-changing therapies to patients faster. As a leader in early clinical research, we combine medical expertise with cutting-edge technology to deliver exceptional results.
We're currently seeking a
BAS Systems Administrator(100%)
to join our Bioanalytical Services (BAS) team in Fehraltorf / Zürich
Key Responsibilities
- Administer and maintain lab systems including LIMS, ELNs, LIS, and other specialized software
- Ensure compliance with GxP standards (GLP, GCP) and regulatory requirements such as 21 CFR Part 11
- Support integration between laboratory instruments and data systems for secure and accurate data transfer
- Manage user roles, access controls, and system configurations
- Monitor and optimize system performance, apply updates, and lead software upgrades
- Serve as the local IT lead for BAS-related infrastructure and project support
- Coordinate with global IT, quality assurance, lab operations, and external vendors
- Participate in audits and provide necessary system documentation
The BAS Systems Administrator plays a key role in ensuring the seamless operation, compliance, and performance of laboratory information systems. Working at the intersection of IT, science, and quality assurance, you will support the digital backbone of our bioanalytical labs—enabling high-quality data that supports global clinical research.
Qualifications
- Bachelor’s degree in IT, Computer Science, Life Sciences, or related discipline
- 3–5 years of experience supporting lab IT systems in a clinical, pharma, or CRO environment
- Hands-on experience with LIMS, ELNs, or other GxP systems
- Strong knowledge of data integrity and compliance frameworks (e.g., GLP, GCP)
- Proficient in Windows Server environments, networking, and SQL databases
- Excellent communication skills in English; German is a plus
- Experience with validated systems and computerized system validation (CSV) is a strong asset
Why Celerion?
- Purpose-Driven Work: Support groundbreaking clinical research that improves lives
- Collaborative Culture: Partner with international teams across IT, lab sciences, and compliance
- Professional Development: Grow your expertise in regulated, high-impact environments
- Global Reach, Local Impact: Be part of a world-class organization - right here in Zürich
Are you ready to make a meaningful impact in drug development and research?
Apply now and join Celerion in shaping the future of health: https://www.celerion.com/careers
