IT Lab Systems Specialist – QC
Il y a 4 heures
Geel, Flanders, Belgique
Pauwels Consulting
Temps plein
Gratuit avec email ou Google
Enregistrez cette offre et organisez votre recherche
Créez un compte gratuit pour enregistrer des offres d'emploi, créer des alertes et revenir à cette liste depuis votre tableau de bord.
Gratuit avec email ou Google
En continuant, vous acceptez nos Conditions d’utilisation & Politique de confidentialité.
pOur client, a leading pharmaceutical company, is seeking an experienced IT Lab Systems Specialist to manage IT infrastructure and software within regulated laboratory environments. The project focuses on supporting quality control and manufacturing science departments to ensure system reliability, performance, and compliance. The role combines hands-on technical management with a strong focus on data integrity and business continuity. /p br/ ul liManage servers, desktops, and workstations within specialized laboratory environments. /li liMaintain and support laboratory software and associated IT infrastructure components. /li liPerform installation, configuration, maintenance, and upgrades of laboratory applications. /li liProvide technical support, troubleshooting, and system performance evaluations. /li liPrepare requirements, architecture design specifications, and installation instructions for laboratory systems. /li liEnsure compliance with bGMP /b, bGAMP 5 /b, and bData Integrity /b requirements across all platforms. /li liManage system security, archiving requests, and disaster recovery testing to ensure business continuity. /li /ul br/ ul liYou have 10+ years of relevant experience in IT infrastructure and laboratory system support. /li liYou possess advanced knowledge of bWindows Server /b, bActive Directory /b, bTCP/IP /b, and general bIT infrastructure /b. /li liYou bring experience in the installation and troubleshooting of bMicrosoft operating systems /b and scripting with bPowerShell /b or bDOS /b. /li liYou're familiar with managing client-server applications within a regulated pharmaceutical environment. /li liYou have a structured working approach with strong documentation and interpersonal skills. /li liYou are fluent in bDutch /b and bEnglish /b. /li /ul br/ h3Nice to Haves /h3 br/ ul liKnowledge of bGAMP 5 /b, b21 CFR Part 11 /b, and validation or qualification methodologies. /li liPossession of relevant bMicrosoft certifications /b. /li /ul br/