Role Overview

The Computer System Validation (CSV) Specialist helps to ensure IFF Pharma Solution’s compliance with company policies, procedures, and industry guidance. The CSV Specialist will risk assess systems, review change requests and test scripts, draft protocols and initiate and review GMP documentation revisions. This role will be based remotely.

Job Requirements

Responsibilities:

• Coordinate with a multi-disciplinary validation team and be responsible for the validation of automated equipment and control systems.
• Initiate/update GxP and Risk Assessments of computerized systems.
• Create and modify validation documentation including but not limited to criticality assessments, validation plans, user requirement specifications, functional and design specifications, traceability matrices, and CSV protocols (IQ, OQ, PQ).
• Write reports which summarize the results of the protocol execution...