Product Quality Associate, IMP

☞ Argenx

Ver: 125

Día de actualización: 16-11-2025

Ubicación: Ghent East Flanders

Categoría: Mecánica / Técnica Mantenimiento

Industria:

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Contenido de trabajo

To further strengthen our Quality team, we are looking for an experienced and motivated Product Quality Associate, IMP. The Product Quality Associate, IMP will play a role in further build out of GMP quality infrastructure at argenx in close collaboration with internal business teams and will be responsible to ensure the quality oversight of CMO’s involved in secondary packaging and labeling of IMP batches, and to follow-up on the timely completion of the Batch Record Review of IMP batches.

This position can be filled in permanently or through consultancy.

Key Accountabilities and Responsibilities:

  • In close collaboration with external and internal manufacturing and supply teams from both CMO and the company:
    • review of executed batch record documentation of IMP batches and support release of IMP for clinical studies ensuring timelines are met
    • review of deviation investigations related to manufactured batches and related corrective and preventive actions
    • review of change control related to manufacturing processes and related effectiveness checks
    • review and support assessment of temperature excursions
    • support in compiling of submission dossiers for Clinical Trial Applications
  • Monitoring of the performance of the manufacturing processes through metrics
  • Contributes to internal and external audit planning and follow-up.
  • Support the further build-out of quality processes and systems.
  • The role may also support the QA team with additional ad hoc project support

Desired Skills and Experiences:

  • 3y+ experience in a quality assurance role, dealing with biopharmaceuticals with experience in biological manufacturing operations.
  • Experience with Batch Record Review is a plus.
  • Experience with working in an outsourced model, closely collaborating with a CMO is and asset.
  • Experience with audits is a plus.
  • Knowledge of FDA and EU regulations and ICH Guidelines.
  • Strong technical mastery, analytical and investigation skills.
  • Accurate in execution and reporting, quality-minded.
  • Able to work effectively together with both internal and external stakeholders.
  • Able to operate in a dynamic surrounding of a fast growing biotech company with challenging timelines.
  • Fluent in English – our working language.

Offer:

  • A competitive salary package with extensive benefits
  • Front seat in the development of therapeutic antibodies
  • A work environment in a human-sized, dynamic and rapidly growing biotech company
  • Possibility to work remotely with limited travelling required
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Plazo: 31-12-2025

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