GMP QC Lab Technician – Testing & Inventory

WuXi AppTec

Couvet

Vor Ort

CHF 65.000 - 90.000

Vollzeit

14 Tage+
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Zusammenfassung

WuXi AppTec in Neuenburg/Couvet seeks a QC Laboratory Associate to support inventory management, ordering of test supplies, and GMP-related documentation. The role includes basic lab work and analytical testing such as IR, pH, conductivity, TOC, titration, and weighing, along with archiving to maintain GMP status.

You will ensure EHS compliance, manage reagents, coordinate with suppliers, assist equipment calibration, and contribute to SOP creation and new reagent qualification.

Qualifikationen

  • Federal Certificate of Capacity or Maturity in Chemistry and/or Biology.
  • 1–2 years of GMP experience.
  • Good knowledge and interpretation of cGMP and related regulations.
  • Strong writing skills.
  • Excellent teamwork and collaboration.
  • Proficiency in English and French.
  • Knowledge of common office software.

Aufgaben

  • Participates in inventory management and ordering of test-related supplies for GMP release.
  • Performs dedicated analytical testing (IR, pH, conductivity, TOC, titration, weighing, etc.).
  • Performs basic laboratory tasks (buffer prep, growth promotion testing, waste disposal, washing dishes, lab cleaning).
  • Supports management in supplying consumables and maintaining relationships with suppliers.
  • Supports equipment maintenance/calibration and archiving in QC Lab.
  • Writes/updates standard operating procedures in the relevant field.
  • Creates/verifies GMP documents and supports selection, purchase, and commissioning of reagents and consumables.
  • Acts as SME for defined areas and may take on special tasks or projects.

Kenntnisse

cGMP knowledge
Technical writing
Team player
English
French
Office software

Ausbildung

Federal Certificate of Capacity or Maturity in Chemistry/Biology

Jobbeschreibung

WuXi AppTec in Neuenburg/Couvet seeks a QC Laboratory Associate to support inventory management, ordering of test supplies, and GMP-related documentation. The role includes basic lab work and analytical testing such as IR, pH, conductivity, TOC, titration, and weighing, along with archiving to maintain GMP status.

You will ensure EHS compliance, manage reagents, coordinate with suppliers, assist equipment calibration, and contribute to SOP creation and new reagent qualification.

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