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 associated with equipment integration. Utilize digital validation management systems, including ALM platf...