




Job Summary: The professional will be responsible for conducting training sessions, drafting and reviewing quality management documents, guiding interns, and ensuring compliance with Good Manufacturing Practices. Key Highlights: 1. Conducting operational and technical training 2. Drafting and reviewing documents of the Quality Management System 3. Guiding and supervising interns * Conduct operational and technical training within the area to disseminate and standardize validation knowledge. * Draft and review documents of the Quality Management System. * Guide and supervise the technical activities of interns. * Control and improve the assigned validation activities. * Stay updated on current legislation and propose adjustments and improvements to ensure compliance. * Critically analyze received data and information to support decision-making. * Guide interfacing departments regarding understanding and compliance with Good Manufacturing Practices. **Requirements:** * Bachelor's degree in Chemistry, Pharmacy, or related fields. * GMP (Good Manufacturing Practices) \- Ensure compliance with GMP. * Ability to write technical documentation clearly and concisely. **Working Hours:** Monday to Friday, from 3:00 PM to 11:56 PM, and alternate Saturdays from 11:00 AM to 5:00 PM. Employment Type: Full-time CLT Salary: R$2\.947,40 \- R$4\.000,00 per month Benefits: * Medical assistance * Commercial agreements and discounts * Profit-sharing program * Life insurance * Transportation allowance Work Location: On-site


