9 часов назад
QC System Expert (LabWare LIMS)
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
QC System Expert (LabWare LIMS): Deploying and maintaining QC digital systems, laboratory equipment records, and GxP-compliant qualification processes in a Singapore quality control laboratory with an accent on data integrity, validation, and regulatory compliance. Focus on administering LabWare LIMS and CMMS, investigating quality events, managing CAPAs and change controls, and supporting audits and inspections.
Location: Singapore
Company
is an R&D-driven, AI-powered biopharma company developing medicines and vaccines.
What you will do
- Represent the Singapore site in global Business Operating Communities for QC digital core models and coordinate local communication.
- Deploy, maintain, and administer LabWare LIMS and other GxP laboratory computerized systems.
- Maintain QC equipment and system master data, access controls, preventive maintenance, calibration schedules, and equipment histories in the CMMS.
- Execute and document qualification, validation, maintenance, UAT, risk assessment, traceability, deviation, and reporting activities.
- Investigate quality events, data discrepancies, deviations, and system issues; implement CAPAs, remediation actions, and change controls.
- Provide end-user training and support during regulatory inspections and audits, while driving continuous improvement in QC support processes.
Requirements
- Experience with QC digital tools, laboratory computerized systems, and technical system administration.
- Practical knowledge of LabWare LIMS, CMMS, GxP asset qualification, equipment maintenance, and calibration.
- Ability to prepare and review validation protocols, user acceptance tests, qualification deliverables, reports, and related quality documentation.
- Knowledge of cGMP, data integrity, compendial compliance, regulatory requirements, and HSE standards.
- Ability to investigate quality control events and discrepancies and implement CAPA and remediation actions.
- Work is based in Singapore in a regulated laboratory environment.
Culture & Benefits
- Work at the intersection of scientific research, quality control, and digital transformation.
- Represent a local site in global governance forums while owning local QC digital deployments.
- Contribute to compliant, reliable medicines and vaccines that reach patients.
- Equal-opportunity workplace with a focus on progress, inclusion, and scientific innovation.
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