




Position Summary: We are seeking a Validation Analyst for an international pharmaceutical laboratory focused on continuous improvement and execution of validation activities. Key Highlights: 1. Key role in continuous improvement at an international pharmaceutical laboratory 2. Responsible for executing and coordinating various validations 3. Active participation in corrective and preventive actions At VITALINE, an international pharmaceutical laboratory specialized in the manufacturing of ophthalmic products, we are currently looking for 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 course in GMP. Training course in Validations/Qualifications. Responsibilities: Support the execution and monitoring of validation activities. Maintain up-to-date documentation for the Quality Management System of the Validation area. 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 Master Validation Plan. Statistically analyze and evaluate results obtained from validation studies. Monitor Quality Control analyses and scheduled training programs. Participate in corrective and preventive actions related to the area. Benefits: Formal employment with all statutory benefits under the General Regime. 100% covered lunch. 100% covered transportation to the plant. Continuous training and development. Opportunity to join a leading pharmaceutical company in the northern region of the country. Working Conditions: Work Location: Paita - Piura. -Requirements- Minimum Education: University Graduate 1 year of experience Keywords: analyst
