regulatoryRaritan, NJ
Global IM CSV Quality Lead | System Validation & Compliance
Global IM CSV Quality Lead | System Validation & Compliance
Global IM CSV Quality Lead | System Validation & Compliance
regulatoryRaritan, NJ
yesterday
Pharmaceutical Preparation ManufacturingBiological Product (except Diagnostic) ManufacturingIn-Vitro Diagnostic Substance Manufacturing
Apply for this role →Johnson & Johnson is seeking an IM CSV Quality Lead to assess, implement, and improve the computer system validation strategy across GxP activities. The role ensures systems are validated and compliant with EU GMP Annex 11, FDA 21 CFR Part 11, and J&J standards.
This position may be based at listed locations or another J&J IM Supply Chain site, requiring global collaboration and strong leadership in CSV initiatives.
Also on the board Same function, level within a rung
Level
Manager
Location
Raritan, NJ
Occupation
Quality Control Systems Managers
Industry
Pharmaceutical Preparation Manufacturing
Posted
yesterday