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Job Summary: A professional responsible for developing, updating, and reviewing analytical technical documentation to ensure product quality, in compliance with guidelines and regulations. Key Highlights: 1. Focus on veterinary product quality and animal welfare. 2. Award-winning company recognized as one of the "Best Companies to Work For". 3. Essential role in Quality Control documentation. **Description**: For over 30 years, we have been committed to delivering the **best in veterinary medicine**, **research**, and **science** to all our partners—professionals who, every day, strive to bring **care to animals**. We understand that, to achieve this, we must first value human relationships, recognizing our dedicated employees whose commitment makes our work possible and drives our daily progress. We have been honored among the **"Best Companies to Work For"** by Great Place to Work Brazil in the Industry and São Paulo 2025 rankings, and in the Agribusiness 2021 ranking. Achieving this recognition confirms that we are on the right path. Join our team! **Opportunity:** QC Analyst \- Technical Documentation \- Junior **Work Location:** Louveira/SP (On-site) **What are the requirements?** * Degree in Pharmacy, Chemistry, or related fields; * Experience in audits and validation of analytical methodologies; * Preferred: training in Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP); * Practical experience in developing and reviewing analytical documentation for raw materials, finished products, and packaging materials; * Experience in developing and reviewing procedures, methods, and validation documentation for analytical methodologies within the scope of Quality Control; * Intermediate English \- Reading and Interpretation. **What are the main responsibilities?** Responsible for developing, updating, and reviewing documentation for raw materials, finished products, and packaging materials (Analytical Methods, Technical Specifications, Working Sheets, and Analytical Certificates), ensuring the quality of products made available for sale, in accordance with Good Manufacturing Practice guidelines and applicable local and international regulatory requirements for Quality Control. Review raw data (working sheets) and analytical certificates for finished products, raw materials, and packaging materials, and release materials in the ERP system, aiming to ensure product quality and customer satisfaction. Develop and review documentation for R&D raw materials for inclusion of new suppliers or new materials (Analytical Methods, Technical Specifications, and Analytical Certificates), to determine whether prospective raw materials meet the required quality standards to guarantee product quality and customer satisfaction. Prepare reports/certificates for products intended for international commercialization (export/COMEX). Review annexes of department-related procedures according to Good Manufacturing Practice guidelines, aiming to ensure product quality and customer satisfaction. Collect data and complete annexes for raw materials controlled under Ordinance 344/98 and IN 35/17 for submission to the Technical Department. Support and participate in audits through preparation, review, and presentation of required documentation, ensuring its consistency and implementation of agreed actions, as well as conducting critical evaluations regarding the implementation of all necessary requirements. Employment Type: Full-time Compensation: R$1,00 \- R$2,00 per month Benefits: * Medical assistance * Dental assistance * Free parking * Life insurance * Meal allowance * Food voucher * Transportation voucher Work Location: On-site
