VALIDATION ANALYST

Description

Position Summary: We are seeking an analyst to execute, document, and monitor process and cleaning validation activities in the pharmaceutical industry, ensuring compliance with GMP and quality standards. Key Highlights: 1. Execution and monitoring of process and cleaning validation 2. Participation in qualification of equipment and systems 3. Ensuring compliance with GMP and pharmaceutical regulations An analyst is required to execute, document, and monitor process and cleaning validation activities, ensuring compliance with GMP, 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 applicable GMP guidelines, FDA, EMA, PIC/S, and ICH requirements. * 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. Work Location: On-site employment