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Quality Engineering- Compliants

Job description

We’re partnering with a high-growth, global life sciences manufacturer at the forefront of bioprocessing and single-use technologies.

They’re hiring a Quality Engineer to drive quality performance across complex, GMP manufacturing operations supporting leading biopharma customers.


The Role

  • Lead quality investigations (complaints, non-conformances, sterility issues)
  • Own root cause analysis + CAPA delivery
  • Partner cross-functionally across Manufacturing, Engineering, R&D, and Supply Chain
  • Drive continuous improvement (Lean / Six Sigma / SPC)
  • Act as key interface for customer, supplier, and regulatory quality topics
  • Support GMP, cleanroom, and validation-driven manufacturing processes

What They Need

  • Experience in biotech / pharma / medtech manufacturing environments
  • Strong grounding in QMS (CAPA, change control, deviations, validation)
  • Exposure to GMP and ISO (9001 / 13485 / FDA)
  • Proven ability to solve complex manufacturing quality issues
  • Comfortable operating in a fast-paced, cross-functional environment

Why This Role

  • High-impact role supporting cutting-edge biopharma manufacturing
  • Exposure to complex, high-value products and global customers
  • Opportunity to drive real operational and quality improvements at scale