QC Analyst

Il y a 2 jours

HeistopdenBerg, Antwerpen, Belgique Arcadis Temps plein 40 000 € - 60 000 € Contrat

As a QC Analyst, you will perform analytical testing on pharmaceutical products and ensure accurate reporting of results within a GMP-regulated laboratory environment.

Responsibilities

  • Perform and evaluate analytical tests including HPLC, GC, TLC, pH, spectroscopy, dissolution, microscopy, density, and viscosity testing.
  • Accurately document test results in the LIMS system.
  • Review analytical results generated by fellow analysts.
  • Report out-of-specification results to the Senior Analyst or Supervisor.
  • Follow cGMP guidelines and laboratory SOPs.
  • Support laboratory housekeeping, stock management, and inventory control.
  • Assist with training activities and onboarding of new team members.

Profile

  • Bachelor's degree in a scientific discipline (Chemistry, Biochemistry, Biotechnology, Pharmaceutical Sciences, or similar).
  • Minimum 2 years of experience in a GMP laboratory is an asset.
  • Hands-on experience with HPLC is required.
  • Knowledge of Waters HPLC systems is a plus.
  • Familiarity with analytical laboratory techniques.
  • Good knowledge of MS Office applications.
  • Good command of English.
  • Able to work in a shift-based environment.

Skills

  • Strong attention to detail and accuracy.