Validation Analyst

Description

Position Summary: A leading pharmaceutical company is seeking a Validation Analyst to ensure control of facilities, equipment, systems, and manufacturing processes through qualification and validation (DQ, IQ, OQ, PQ) under GMP. Key Responsibilities: 1. Ensure control of facilities, equipment, and critical systems. 2. Execution and documentation of qualification and validation activities. 3. Work in accordance with Good Manufacturing Practice (GMP) guidelines. A prominent pharmaceutical sector company is currently seeking a Validation Analyst responsible for ensuring the state of control of facilities, equipment, critical systems, and manufacturing processes through the execution and documentation of qualification and validation activities (DQ, IQ, OQ, PQ), in compliance with Good Manufacturing Practice (GMP) guidelines and the Validation Master Plan. Requirements * Technical or technological professional degree in Pharmaceutical Chemistry or related fields. * Experience in pharmaceutical process validation. * Knowledge of qualification (IQ, OQ, PQ). * GMP. Employment Type: Full-time Work Location: On-site employment