Key Responsibilities
• Perform Process Validation activities. Schedule own tasks to be performed as well as tasks for other Specialists as determined by the Validation Manager
• Perform change control assessments for GMP equipment and associated validation activities to ensure compliance with regulatory requirements
• Program, organize, and maintain Validation equipment and supplies.
• Demonstrate a thorough understanding of validation procedures for Qualification. Develop validation protocols from Validation plans and engineering documents.
• Provide strong technical expertise when reviewing and approving SOPs, protocols, change controls, deviations
• Perform assigned Quality Systems activities including: Document Management System (DMS), Trackwise system (Change Control, Deviations, CAPA, etc.).
• Perform other duties as assigned

Key Requirements
• Bachelor’s Degree in Science or technical discipline
• More than 5 years of experience in validation, preferably in a batch...
Singapore

Salary Criteria