VALIDATION ANALYST

Description

Job Summary: We are seeking a Validation Analyst to execute and document process and cleaning validation activities, ensuring compliance with GMP and pharmaceutical quality standards. Key Highlights: 1. Execute and document process and cleaning validations 2. Ensure compliance with GMP and pharmaceutical regulations 3. Participate in qualification of equipment and production systems A Validation Analyst is required to execute, document, and follow up on process and cleaning validation activities, ensuring compliance with GMP, regulatory requirements, and pharmaceutical industry quality standards. **Key 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 production processes.** * Manage change controls associated with validated processes, equipment, and procedures. * Ensure compliance with GMP, 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. Work Location: On-site employment