




Job Summary: We are seeking a detail-oriented, responsible, and proactive Quality Analyst eager to contribute to process excellence, with a strong focus on regulatory compliance, continuous improvement, and product safety. Key Highlights: 1. Maintain and improve the Quality Management System (QMS) 2. Focus on regulatory compliance, continuous improvement, and product safety 3. Regulated environment governed by ANVISA, with technical training We are looking for a **Quality Analyst** who pays close attention to detail, demonstrates responsibility, and is committed to enhancing the excellence of our processes. This professional will be a **key contributor** to maintaining and improving the Quality Management System (QMS), focusing on **regulatory compliance, continuous improvement**, and **product safety**. If you possess a **solid technical education, analytical capability, organizational skills, and interest in working within an ANVISA-regulated environment**, this opportunity is for you. **Key Responsibilities:** * Support maintenance and improvement of the Quality Management System (QMS), ensuring compliance with RDC 665/2022 requirements and Good Manufacturing Practices (GMP); * Participate in the development, review, and control of quality documents, such as Standard Operating Procedures (SOPs), work instructions, records, and forms; * Support internal audit execution, contributing to corrective action plans and follow-up on resolutions; * Conduct inspections and verifications in production processes, ensuring product conformity with technical specifications and regulatory requirements; * Monitor quality performance indicators (KPIs), analyze data, and propose continuous improvement actions; * Assist in investigating nonconformities, technical complaints, and deviations using methodologies such as 5 Whys, Ishikawa, or similar; * Support implementation of quality programs, such as 5S, continuous improvement, and change control; * Contribute to onboarding and technical training on quality-related topics and sanitary regulations. **Requirements:** * Currently enrolled in or graduated from a Bachelor’s degree program in Engineering, Pharmacy, Biomedicine, Quality Management, or related fields; * Basic knowledge of quality tools (PDCA, 5 Whys, Ishikawa Diagram, etc.); * Familiarity with ANVISA regulations and applicable ISO standards is desirable; * Proficiency in Microsoft Office suite; * Strong communication and organizational skills. **Preferred Qualifications:** * Prior experience in regulated sectors (healthcare products, pharmaceutical, or hospital industries); * Training in quality, GMP, or internal auditing. **WORK SCHEDULE:** Monday to Thursday: 7:00 AM to 12:00 PM and 1:00 PM to 5:00 PM Friday: 7:00 AM to 12:00 PM and 1:00 PM to 4:00 PM Benefits: – Meal allowance; – Health insurance; – Dental insurance; – Pharmacy benefit plan; – Birthday day off; – Weekly breakfast; – Fruit day.


