Senior CIP/CQV Engineer - GMP Biotech Systems
Verista
Verista is seeking a Clean-in-Place (CIP) Engineer on site in Apex, NC, to lead commissioning and qualification for CIP systems within GMP environments. You will develop C&Q documentation, coordinate with design engineers, and ensure systems meet quality and safety standards. Responsibilities include leading CIP cycles, URS/QRAES development, IOQ protocols, and collaboration with automation and SME teams to finalize test plans; you will support FATs/SATs and maintain system ownership #J-18808-Ljbffr Verista
Vacancy posted 4 days ago
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