Job Summary: Junior QC Analyst - Technical Documentation responsible for preparing and reviewing analytical documentation to ensure product quality in accordance with GMPs and applicable regulations. Key Highlights: 1. Focus on quality and regulatory compliance 2. Development and review of technical documentation 3. Participation in audits for quality assurance **Description**: For over 30 years, we have worked to deliver the **best of veterinary medicine**, **research**, and **science** to all our partners, who, day in and day out, strive to bring **care to animals**. We understand that, to achieve this, we must first value human relationships, recognizing our employees who dedicate themselves to making our work happen and progress every day. We have been recognized among the **“Best Companies to Work For”** by Great Place to Work Brazil, in the Industry and São Paulo 2020 ranking and the Agribusiness 2021 ranking; earning this recognition confirms that we are on the right path. Join our team! **Opportunity:** Junior QC Analyst - Technical Documentation **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 preparation and review of analytical documentation for raw materials, finished products, and packaging materials; * Experience in preparation and review of procedures, methods, and documentation for validation of analytical methodologies within the scope of Quality Control; * Intermediate English – Reading and Interpretation. **What are the main responsibilities?** Responsible for preparing, updating, and reviewing documents for Raw Materials, Finished Products, and Packaging Materials (Analytical Methods, Technical Specifications, Working Sheets, and Analytical Certificates), aiming to ensure the quality of products made available for sale, in accordance with Good Manufacturing Practice guidelines and applicable local and international regulatory agency requirements for Quality Control. Perform verification of raw data (working sheets) and analytical certificates for Finished Products, Raw Materials, and Packaging Materials, and release materials in the ERP system, aiming to guarantee product quality and customer satisfaction. Prepare and verify documentation for Research and Development raw materials for inclusion of new suppliers or new materials (Analytical Methods, Technical Specifications, and Analytical Certificates), aiming to determine whether prospective raw materials meet the required quality standards to ensure product quality and customer satisfaction. Prepare reports/certificates for products destined for international commercialization (export/COMEX). Verify annexes of procedures related to the department 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 by preparing, reviewing, and presenting required documentation, ensuring its consistency and implementation of established actions, as well as conducting critical evaluations regarding implementation of all necessary requirements. Employment Type: Full-time Compensation: R$1,00 - R$2,00 per month Benefits: * Medical insurance * Dental insurance * Free parking * Life insurance * Meal allowance * Food allowance * Transportation allowance Work location: On-site