CSV Specialist & Technical Writer - Regulated Life Sciences

A leading consulting firm in life sciences is seeking a Computer System Validation Specialist/Technical Writer to support regulated manufacturing in Pennsylvania. The role involves executing and maintaining Computer System Validation (CSV) activities to ensure compliance with FDA, GxP, and internal quality standards. Candidates need 3–5 years of experience in regulated industries, strong technical writing skills, and the ability to produce clear, audit-ready documentation. This position offers a chance to contribute meaningfully in a collaborative environment. #J-18808-Ljbffr