QA Lead: LIMS Implementation & GMP QC Oversight

Swisslinx

Stein

Vor Ort

CHF 110.000 - 140.000

Teilzeit

vor 44 Stunden
Sei unter den ersten Bewerbenden
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Zusammenfassung

Swisslinx seeks an experienced QA professional to lead QC QA oversight during the implementation of a laboratory execution system (gLIMS) in a Life Sciences setting. You will ensure GMP compliance, review QC documentation, and drive SOP development while coordinating with cross-functional teams.

The role focuses on supporting the QC department, managing deviations, and facilitating QA inspections. Fluent English is required; German is a plus.

Qualifikationen

  • Provide QA oversight and guidance to QC department ensuring GMP compliance and internal procedures.
  • Act as the primary QA contact for the implementation of gLIMS/LIMS.
  • Support cross-functional growth projects and ensure QA deliverables meet timelines.
  • Review and approve GMP-relevant QC documentation including SOPs for gLIMS.

Aufgaben

  • Provide QA oversight and guidance to the QC department, ensuring GMP compliance.
  • Act as the primary QA point of contact for gLIMS/LIMS implementation.
  • Support cross-functional projects and ensure QA/QC deliverables meet timelines.
  • Review and approve GMP-related QC documentation and SOPs for gLIMS.
  • Manage quality activities including change requests, deviations and document management.
  • Write, revise and own SOPs within your area of expertise.
  • Support QC raw data review where required.
  • Ensure compliance with internal quality standards and health authority guidance.
  • Support inspections and audits and contribute to KPI reporting.

Kenntnisse

LIMS implementation
GMP compliance
Quality Assurance
SOP development
CSV/Validation
Regulatory liaison
Project management
Cross-functional collaboration

Tools

gLIMS/LIMS software

Jobbeschreibung

Swisslinx seeks an experienced QA professional to lead QC QA oversight during the implementation of a laboratory execution system (gLIMS) in a Life Sciences setting. You will ensure GMP compliance, review QC documentation, and drive SOP development while coordinating with cross-functional teams.

The role focuses on supporting the QC department, managing deviations, and facilitating QA inspections. Fluent English is required; German is a plus.

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