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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.