VALIDATION ANALYST

Description

Job Summary: We are seeking an analyst to execute, document, and monitor process and cleaning validation activities, ensuring compliance with cGMP and quality standards. Key Responsibilities: 1. Execute and document process and cleaning validation 2. Ensure compliance with cGMP and regulatory requirements 3. Participate in equipment and system qualification We require an analyst to execute, document, and monitor process and cleaning validation activities, ensuring compliance with cGMP, regulatory requirements, and pharmaceutical industry quality standards. **Main Responsibilities:** * Develop, execute, and review process and cleaning validation protocols and reports. * Participate in qualification of equipment and systems (DQ, IQ, OQ, and PQ) related to manufacturing processes. * Manage change controls associated with validated processes, equipment, and procedures. * Ensure compliance with cGMP, FDA, EMA, PIC/S, and ICH guidelines. * Maintain the Validation Master Plan (VMP) documentation up to date. Requirements: Bachelor's degree in Pharmaceutical Chemistry, Chemistry, Chemical Engineering, Microbiology, or related fields. Minimum 1 year of experience in process validation and/or cleaning validation within the pharmaceutical industry. Workplace: On-site employment