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Job Summary: CQ II Analyst - Technical Documentation responsible for ensuring quality standards in veterinary medicine through the preparation and review of documentation, support during audits, and training of employees. Key Highlights: 1. Awarded company as "Best Company to Work For" 2. Essential role in quality and customer satisfaction 3. Participation in Cleaning and Process Validation programs **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 every day. We are awarded among the **"Best Companies to Work For"** by Great Place to Work Brasil, in the Industry and São Paulo 2020 ranking and in the Agribusiness 2021 ranking; achieving this recognition confirms that we are on the right path. Join our team! **Opportunity:** CQ II Analyst - 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; * Desired: Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) training; * Experience with technical documentation focused on Quality Control; * Practical experience in preparing and reviewing analytical documentation for raw materials, finished products, and packaging materials; * Intermediate English - Reading and Interpretation. **What are the main responsibilities?** Responsible for preparing 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 analysis certificates, releasing materials in the system with a focus on maintaining quality and customer satisfaction. Prepares and verifies technical documentation for R&D raw materials to include new suppliers or materials, ensuring compliance with required quality standards. Participates in and supports internal and external audits by preparing, reviewing, and presenting necessary documentation, and by developing, implementing, and monitoring 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 employees on Good Documentation Practices and ERP system usage, providing support to internal customers in resolving queries, defining deadlines, and submitting documents to ensure procedural compliance and record quality. Performs and verifies data collection and completion of annexes related to raw materials controlled by Ordinance 344/98 and IN 35/17 for submission to the Technical Department. Plans and monitors schedules for preparing raw material documents, SOPs, general methods, and finished product documents, keeping Quality Control Documentation area indicators up-to-date and ensuring migration of documents to the Protheus system. Also participates in Cleaning Validation and Process Validation programs, reviewing protocols, reports, and raw data to ensure adherence to established timelines. Employment Type: Full-time Salary: R$1,00 - R$2,00 per month Benefits: * Medical assistance * Dental assistance * Free parking * Life insurance * Meal allowance * Food allowance * Transportation allowance
