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.