Senior Laboratory Interface Administrator

ThermoFisher Scientific

Zaventem

Sur place

EUR 65 000 - 90 000

Plein temps

Il y a 9 jours

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Résumé du poste

Thermo Fisher Scientific in Zaventem, Belgium, seeks a Senior Application Administrator to own the configuration, validation, and lifecycle management of laboratory middleware and instrument interfaces in a regulated GxP environment.

You will lead CSV activities (IQ/OQ/PQ), develop and maintain validation artifacts, support change control, ensure data integrity, and provide production support across LIS and instrument interfaces.

Qualifications

  • Bachelor's degree in IT/CS/Engineering/Medical Technology or related field.
  • 5+ years administering regulated laboratory, healthcare, clinical, or manufacturing apps.
  • 3+ years supporting medical device, instrument, middleware, or lab system integrations.
  • Experience in GxP-regulated environments.
  • Experience with CSV activities (IQ, OQ, PQ).
  • Experience with change control, validation docs, and audit support.
  • Technical skills in LIS and middleware platforms.
  • Experience with Instrument Manager or similar middleware.
  • Knowledge of TCP/IP networking and interface troubleshooting.

Responsabilités

  • Application Administration & Interface Management - Administer middleware apps incl. Instrument Manager and LIS.
  • Configure and maintain instrument interfaces, routing rules, test mappings, and communications parameters.
  • Manage configurations across Development, Test, Validation, and Production environments.
  • Support onboarding of new instruments, analyzers, assays, and third-party interfaces.
  • Configure and maintain TCP/IP, serial, file-based, and other interface methods.
  • Root cause analysis for interface failures and data integrity concerns.
  • CSV - Execute IQ, OQ, PQ activities and validation documentation updates.
  • Maintain validation artifacts, traceability, and evidence packages.
  • Lead end-to-end testing for new/modified interfaces and validate workflow processing.
  • Ensure compliance with 21 CFR Part 11, GDP, CSV and quality procedures.

Connaissances

Validation leadership
Data integrity
Cross-functional communication
Documentation excellence
Attention to detail
Project coordination
Audit readiness
Problem solving

Formation

Bachelor's degree in IT/CS/Engineering/Medical Tech

Outils

LIS and middleware platforms
Instrument Manager
TCP/IP networking
Interface troubleshooting
Electronic document management

Description du poste

Thermo Fisher Scientific in Zaventem, Belgium, seeks a Senior Application Administrator to own the configuration, validation, and lifecycle management of laboratory middleware and instrument interfaces in a regulated GxP environment.

You will lead CSV activities (IQ/OQ/PQ), develop and maintain validation artifacts, support change control, ensure data integrity, and provide production support across LIS and instrument interfaces.

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