Validation Program Lead, cGMP Pharma
Listed on 2026-11-01
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Pharmaceutical
Pharma Engineer, Pharmaceutical Manufacturing -
Quality Assurance - QA/QC
Guerbet is seeking an experienced Validation Manager to lead the Validation department within our pharmaceutical manufacturing operations in North Carolina. You will oversee the complete validation lifecycle, including qualification, validation, requalification, and revalidation programs, partnering with Engineering, MS&T, Operations, QA, and Regulatory Affairs to support manufacturing initiatives.
The role requires deep cGMP pharmaceutical knowledge, especially in parenteral or injectable
This posting is for the Validation Program Lead, cGMP Pharma role at Guerbet, based in NC, United States.
This role is for the Validation Program Lead, cGMP Pharma role at Guerbet.
We are seeking a motivated Validation Program Lead, cGMP Pharma to join Guerbet in NC, United States.
Consider building your career as a Validation Program Lead, cGMP Pharma at Guerbet.
The Validation Program Lead, cGMP Pharma position in the Management & Operations, Engineering field is open for applications.
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