Senior Cleaning Validation Lead – Biologics GMP; Hybrid
Listed on 2026-09-30
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Quality Assurance - QA/QC
i-Pharm GxP in North Carolina is seeking an experienced Cleaning Validation Consultant to lead cleaning validation activities across multiple manufacturing suites ahead of a major regulatory inspection window. You will author and execute validation protocols and manage residue limits while partnering with Quality and Manufacturing to maintain an inspection-ready site.
The role requires 6–10+ years in cleaning validation in GMP pharma/biotech/CDMO environments, with a data-driven approach to
Are you ready to take on the Senior Cleaning Validation Lead – Biologics GMP (Hybrid) role at i-Pharm GxP?
Full responsibilities and requirements are described in the listing above.
Learn more about the Senior Cleaning Validation Lead – Biologics GMP (Hybrid) role in the description above.
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