QA CQV Lead - GMP Biologics, Site Expansion; Equity
Listed on 2026-10-15
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, QA Specialist - Analyst/Manager
CSL Behring is expanding its Kankakee (KAN) site to support Ig production. This role provides quality oversight for the Commissioning and Qualification activities for the M7/8 site expansion, ensuring GMP-compliant planning and execution throughout all CQV phases.
The role requires a degree in a related scientific discipline and at least 5 years in quality/GMP, with strong knowledge of FDA/EU/GxP guidelines and experience in CQV of production facilities and clean rooms.
We are currently recruiting a QA CQV Lead - GMP Biologics, Site Expansion (Equity) for our team in Bradley, IL, United States.
We would love to welcome a new QA CQV Lead - GMP Biologics, Site Expansion (Equity) to our organisation in Bradley, IL, United States.
For the QA CQV Lead - GMP Biologics, Site Expansion (Equity) position at CSL, we are reviewing applications now.
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