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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