Validation Analyst

Description

Job Summary: A leading pharmaceutical company is seeking a Validation Analyst to ensure the state of control of facilities, equipment, systems, and manufacturing processes. Key Responsibilities: 1. Ensure control of facilities and equipment 2. Execution and documentation of qualification and validation (DQ, IQ, OQ, PQ) 3. Work under Good Manufacturing Practices (GMP) 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 accordance with Good Manufacturing Practices (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