**Description**: For over 30 years, we have worked to deliver the **best of veterinary medicine**, **research**, and **science** to all our partners who, every day, strive to bring **care to animals**. We understand that, to achieve this, we must first value human relationships, recognizing our employees who dedicate themselves and make our work happen and progress daily. We have been awarded among the **“Best Companies to Work For”** by Great Place to Work Brazil, in the Industry and São Paulo 2020 rankings and the Agribusiness 2021 ranking; achieving this recognition confirms that we are on the right path. Join our team! **Opportunity:** QC Analyst II – Technical Documentation **Work Location:** Louveira/SP (On-site) **What are the requirements?** * Degree in Pharmacy, Chemistry, or related fields; * Knowledge of HACCP processes; * Experience in audits and validation of analytical methodologies; * Experience with Quality Control procedures and methodologies; * Preferred: training in Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP); * Experience with technical documentation focused on Quality Control; * Practical experience in developing and reviewing analytical documentation for raw materials, finished products, and packaging materials; * Intermediate English – Reading and Interpretation. **What are the main responsibilities?** Responsible for developing and reviewing Standard Operating Procedures (SOPs), General Methods, Specifications, Analytical Methods, and Certificates of Analysis for raw materials, finished products, and packaging materials via the ERP system, ensuring definition of acceptable quality standards for each material. Performs verification of raw data and Certificates of Analysis, releasing materials in the system, with focus on maintaining quality and customer satisfaction. Participates in development and verification of technical documentation for R&D raw materials to onboard new suppliers or materials, ensuring compliance with required quality standards. Participates in and supports internal and external audits, preparing, reviewing, and presenting required documentation, as well as developing, implementing, and monitoring corrective action plans to address identified non-conformities. Monitors Quality Control activities related to the Change Control system, attending meetings and tracking action plans to assess impacts and ensure timely resolution. Trains department staff on Good Documentation Practices and ERP system usage, providing support to internal customers in resolving queries, defining deadlines, and submitting documents, to ensure adherence to procedures and record quality. Performs and verifies data collection and completion of annexes related to raw materials controlled under Ordinance 344/98 and IN 35/17 for submission to the Technical Department. Plans and monitors schedules for developing documentation for raw materials, SOPs, general methods, and finished products, maintaining updated performance indicators for the Quality Control Documentation area and ensuring document migration to the Protheus system. Also participates in Cleaning Validation and Process Validation programs, reviewing protocols, reports, and raw data, ensuring adherence to established timelines. Employment Type: Full-time Salary: BRL 1,000.00 – BRL 2,000.00 per month Benefits: * Medical insurance * Dental insurance * Free parking * Life insurance * Meal allowance * Food voucher * Transportation voucher