Regulated Lab IT Systems Specialist

Our 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...

Pauwels Consulting is seeking an experienced IT Lab Systems Specialist to manage IT infrastructure and software within regulated laboratory environments in Belgium. The role focuses on supporting quality control and manufacturing science to ensure system reliability, performance, and data integrity. The ideal candidate has over 10 years in IT infrastructure...

Bij Select Projects draait alles om jou als consultant. We willen dat jij elke dag met goesting aan de slag gaat, jezelf kan zijn en de ruimte krijgt om te groeien. Als consultant werk je aan uitdagende projecten waar je jouw talent volop kan inzetten en verder ontwikkelen. Je krijgt vertrouwen, autonomie en de kans om bij te leren via opleidingen,...

Job Description As an IT Specialist, Laboratory Systems, you’ll manage and support GMP and non-GMP laboratory systems used by the Quality Control and Manufacturing Science and Technology teams. You’ll provide day-to-day IT support and project assistance across laboratory software, servers, workstations, infrastructure, maintenance, validation,...

Functieomschrijving Als Senior Lab Systems Engineer beheer en ontwikkel je kritische laboratoriumsystemen binnen een farmaceutische productieomgeving. Je ondersteunt zowel GMP- als niet-GMP-laboratoria binnen Quality Control en Manufacturing Science & Technology. Daarbij combineer je operationele ondersteuning met projectwerk rond implementaties, upgrades en...

Ben jij een ervaren CSV- en IT Quality-expert die graag de lat hoog legt voor compliance?We zoeken een Senior CSV Specialist die de kwaliteit, compliance en validatie van IT-systemen en -processen trekt in een internationale farmaceutische omgeving.Validatiestrategieën en -documentatie opvolgen gedurende de volledige levenscyclus van...

Job Description Join Amaris Consulting and contribute to data integrity and compliance projects within the pharmaceutical industry. You will support a key pharmaceutical client in reviewing GxP-regulated analytical equipment and associated computerized systems across Manufacturing and Quality Control (QC). Working alongside site Subject Matter Experts and...

Job DescriptionAct as the primary escalation point for complex MES incidents and production issues.Configure, administer, and optimize MES functionalities supporting GMP manufacturing activities.Perform root cause analysis and implement permanent corrective actions.Support electronic batch records, manufacturing workflows, and production processes.Lead...

Overview PM Group are seeking an experienced Turnover Coordinator to join our pharma construction project team in Geel, Belgium. PM Group is an employee owned, international project delivery firm. We are world leaders in the pharma, food, medtech and mission critical sectors. From our network of offices in Europe, Asia and the US, we work with the world's...