We are seeking an experienced Validation / Commissioning Specialist to support a special project involving the replacement and qualification of load cells in a pharmaceutical manufacturing environment.

Project Overview

The selected candidate will support commissioning, qualification, validation, and documentation activities associated with the installation and startup of the new system.

Position Responsibilities

• Execute commissioning and qualification activities for equipment upgrades and system replacements.
• Support installation, operational, and performance qualification protocols (IQ/OQ/PQ).
• Ensure compliance with current cGMP regulations and pharmaceutical industry standards.
• Develop and review validation, commissioning, and technical documentation.
• Coordinate validation activities within a regulated manufacturing environment.
• Support computer system validation (CSV) activities associat...