Validation Analyst

Description

Position Summary: We are seeking a Validation Analyst for a pharmaceutical laboratory, focused on continuous improvement, execution and monitoring of validations, and document management. Key Highlights: 1. Key support in the execution and monitoring of validation activities 2. Management and updating of Quality Management System documentation 3. Active participation in corrective and preventive actions within the department At VITALINE, a pharmaceutical laboratory specializing in the manufacturing of ophthalmic products with international presence, we are currently seeking a professional to assume the role of Validation Analyst, oriented toward continuous improvement. Requirements: Bachelor's degree in Pharmacy and Biochemistry, Industrial Engineering, or related fields. 2 years of experience in the position. Training or course in Good Manufacturing Practices (GMP). Training or course in Validations/Qualifications. Responsibilities: Support the execution and monitoring of validation activities. Maintain up-to-date documentation of the Validation Department's Quality Management System. Coordinate and organize activities related to validation processes. Execute validations of manufacturing, cleaning, sanitization, sterilization, and computerized systems. Develop protocols and reports, and monitor the Validation Master Plan. Statistically analyze and evaluate results obtained from validation studies. Monitor Quality Control analyses and scheduled training sessions. Participate in corrective and preventive actions related to the department. Benefits: Formal employment registration with all statutory benefits under the General Regime. 100% covered lunch. 100% covered transportation to the plant. Ongoing training and professional development. Opportunity to join a leading pharmaceutical company in the northern region of the country. Working Conditions: Workplace: Paita - Piura. -Requirements- Minimum Education: University graduate 1 year of experience Keywords: analyst