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Quality control Laboratory Assistant (contingent worker)

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Onsite

Quality control Laboratory Assistant (contingent worker)

WuXi AppTec

Quality control Laboratory Assistant (contingent worker)

Skills

Inventory Management

15 days ago

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Important information


Contract type:

Permanent

Work mode:

Onsite

Published on:

9 October 2026

What they need


Job Summary This position is responsible for participating in inventory management and ordering of test-related supplies that is required for release of raw and packaging materials, final product and stability samples as well as all IPC testing. Additional responsibilities can be to perform basic laboratory work as well as the support for maintenance of dedicated equipment.

As a QC team member, the person filling this position supports all activities to continuously maintain the GMP status of the QC Laboratory.

Essential Job Functions

  • This position is responsible for ensuring all EHS requirements in the laboratory:

  • Respect EHS procedures and rules

  • Report immediately all incidents and near-misses to the management and/or to the EHS representative people

  • Responsible for chemical reagents management (Ordering – Inventory)

  • Performs dedicated analytical testing (IR, pH, conductivity, TOC, titration, weighing, etc.).

  • Performs basic laboratory work (buffer preparation, growth promotion test, waste disposal management, washing of lab dishes, cleaning of the labs etc.

  • Supports management supply of consumables.

  • Supports maintenance/calibration of equipment and keeps relationship with suppliers.

  • Performs archiving activities for QC Lab.

  • Writes specific standard operations procedures (in his field of activity)

  • Create and/or verification of GMP documents

  • Supports selection, purchase and commissioning of new reagent - consumables.

  • Acts as a SME for defined areas

  • Can be assigned special tasks and project work

Job Requirements Experience / Education

  • Federal Certificate of Capacity or Maturity with Chemistry and/or Biology knowledge
  • 1 — 2 years of work experience in a GMP environment

Knowledge / Skills / Abilities

  • Good knowledge and interpretation of cGMP and regulations applicable to the Quality Control environment
  • Good writing skills.
  • Excellent team spirit.
  • Good knowledge in English and French.
  • Knowledge of most common office software.

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. Employees holding this position will be required to perform any other job-related duties as requested by Management.

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