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Laboratory Coordinator & Hub Manager

INSTITUUT VOOR TROPISCHE GENEESKUNDE in ANTWERPEN
Vaste jobs
Online sinds 7 apr. 2026
For a detailed introduction, background and job description, we refer to the PDF document Set-up and manage the ‘Cell Isolation and Imaging Hub’, assist in its daily laboratory activities (e.g. cell isolation/enrichment, flow cytometry) Coordinate usage of shared equipment within the department, including maintenance contracts and related budgetary activities, in collaboration with the purchase and quality departments Assist in ordering and exporting of reagents/equipment, drafting tender procedures, negotiating with major suppliers, and audit readiness, in collaboration with the purchase and logistic departments Provide technical advice in laboratory set-up and drafting of biosafety files. More specifically, you will play a central role in the preparation and roll-out of new laboratory infrastructure in ITM’s extension plans Implement (bio)safety and environmental requirements in collaboration with the prevention unit of ITM (e.g. introduction of new activities/instruments/chemicals) Aid in proper health and safety introduction for new users and regulation of lab access to the BSL-1/2/3 laboratories Aid in implementation of QA systems (including calibration activities) for both non-regulated as well as ISO accredited activities in collaboration with QA unit Actively look for opportunities for improvement, help streamline activities across the departments, and attend relevant conferences/meetings & trainings.

QC scientist HPLC Compendial techniques

LabCorp in MECHELEN
Vaste jobs
Online sinds 28 apr. 2026
A), and assay documentation Oversee assay execution, troubleshoot analytical challenges, and guide teams through unexpected scientific issues Review and approve regulatory data, assay based quality documents (Quality Events, risk assessments, CAPA’s, change controls and Out of Specification) and investigation reports Coordinate laboratory activities and ensure work aligns with SOPs, GMP, and client expectations With understanding of all methodologies for a Client project you will formulate reports using approved data that fulfils the protocol design and all regulatory expectations Track study progress, anticipate risks, and drive timely resolution of issues Lead in depth scientific and/or quality discussion with the client and/or internal customer Manage multiple batch testing, release testing, sample analysis, stability, assay development and validations/transfers studies Mentor and support colleagues, contribute to training materials, and help strengthen scientific capability across the team Represent Labcorp at conferences, client meetings, and scientific forums Navigate the regulatory framework to ensure that the client programs are conducted with scientific integrity, to meet the defined milestones along the drug development pathway Identification and communication of scientific and regulatory developments to QC operations and the wider senior scientific group (e.g. Method Development/Clients) Maintain in depth knowledge of relevant scientific and GMP guidelines and knowledge of the relevant area of the drug development process Maintain in depth knowledge of regulatory expectations and multiple method capabilities.