About this opportunity
Katalyst CRO lists this Senior CSV Engineer for GMP Validation (Biopharma) opportunity in boston, Massachusetts. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Katalyst CRO seeks experienced CSV Engineers for on-site validation support in a regulated biopharmaceutical environment. The role centers on Computer System Validation while also supporting equipment qualification and broader CQV activities as priorities require.
Consultants will validate documentation and execute protocols, assess systems against GMP requirements, document results, investigate discrepancies, and work across Engineering, Quality, Manufacturing, Automation, IT, and system owners.
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Worksite address
boston, MA, 02298, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.