Senior Application Administrator
$31,200–$31,200 year
On-siteZaventem, Flanders, Belgium
Zaventem, Flanders, BelgiumOn-siteFull Time$31,200–$31,200 yearSenior LevelLarge
Full TimeSenior LevelLarge
Job Summary
Administer, configure, and validate laboratory middleware and instrument interfaces within a GxP environment, ensuring compliance with 21 CFR Part 11 and data integrity standards. Execute change control, IQ/OQ/PQ activities, and end-to-end testing for instrument-to-LIS integrations while supporting audit readiness and production stability. Partner with Laboratory Operations, Quality Assurance, and IT teams to manage validation documentation, troubleshoot interface failures, and onboard new instruments across multiple locations.
Required Qualifications
- Bachelor's degree in Information Technology, Computer Science, Engineering, Medical Technology, Clinical Laboratory Science, or related discipline
- Equivalent combination of education and relevant experience
- 5+ years of experience administering regulated laboratory, healthcare, clinical, or manufacturing applications
- 3+ years of experience supporting medical device, instrument, middleware, or laboratory system integrations
- Experience working in GxP-regulated environments
- Experience executing or supporting CSV activities including IQ, OQ, and PQ
- Experience with change control, validation documentation, and audit support
- Laboratory Information Systems (LIS) and middleware platforms
- Instrument Manager or comparable middleware applications
- Medical device and laboratory instrument interfacing
- TCP/IP networking, serial communications, and interface troubleshooting
- Configuration management and controlled software deployment practices
- Validation documentation and testing methodologies
- Microsoft Office applications and electronic document management systems
Desired Qualifications
- Experience in clinical laboratory, central laboratory, pharmaceutical, biotechnology, CRO, or medical device environments
- Knowledge of HL7, ASTM, or other healthcare messaging standards
- Familiarity with GAMP 5 principles
- Experience supporting quality control systems and laboratory workflows
- Knowledge of laboratory assay validation and reportable range management
- Experience with audit trail review and data integrity assessments
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