QC Lab Coordinator: Documentation, Sampling & Compliance

Incyte

Yverdon-les-Bains

Vor Ort

CHF 70.000 - 95.000

Vollzeit

Vor 2 Tagen
Sei unter den ersten Bewerbenden
Bewerbungsgenerator

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Zusammenfassung

Incyte is seeking a QC Lab Coordinator to support Quality Control through administrative tasks such as documentation management, procurement, goods receipt, shipment arrangements, and invoice reconciliation. The role includes assisting with sample handling and basic analytical support for physico-chemical analyses, while upholding safety and compliance in a GMP environment.

The candidate will manage QC samples, purchase requests, reagent inventory, and QA-aligned document workflows,

Qualifikationen

  • Diploma in analytical chemistry or equivalent.
  • GMP environment experience in pharma/biotech.
  • Rigorous, organized and proactive.
  • Fluent French with written English preferred.
  • Strong safety discipline in lab work.

Aufgaben

  • Receive, aliquot and record QC samples in LIMS; store and ship as needed.
  • Manage purchase requests: quotes, PO creation, goods receipts and invoicing.
  • Oversee reagents/consumables: tracking, labeling, inventory, kanban, release coordination.
  • Coordinate goods delivery and inter-department communication.
  • Create and maintain quality documents (SOPs, WI), with QA review and archiving.
  • Ensure cross-team communication within QC, Manufacturing, Supply Chain, QA, and providers.
  • Support inspections/audits and respond to observations; assist with basic lab work.

Kenntnisse

GMP experience
Analytical chemistry
Documentation management
LIMS knowledge
Team collaboration
Proactivity
Safety awareness
English (written)

Ausbildung

Diploma in analytical chemistry

Jobbeschreibung

Incyte is seeking a QC Lab Coordinator to support Quality Control through administrative tasks such as documentation management, procurement, goods receipt, shipment arrangements, and invoice reconciliation. The role includes assisting with sample handling and basic analytical support for physico-chemical analyses, while upholding safety and compliance in a GMP environment.

The candidate will manage QC samples, purchase requests, reagent inventory, and QA-aligned document workflows,

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