Quality Specialist - Risks

Description

Job Summary: The professional will manage the Pharmaceutical Quality System, with a focus on Quality Risk Analysis, investigations, and continuous improvement in the pharmaceutical industry. Key Highlights: 1. Management of the Pharmaceutical Quality System. 2. Focus on Quality Risk Analysis and Good Manufacturing Practices (GMP). 3. Participation in continuous improvement and innovation projects. At **Hypofarma**, caring for lives is what drives us after **77 years**. We are a Minas Gerais-based pharmaceutical manufacturer specializing in **injectable medications for the hospital segment**, committed to quality, responsibility, and innovation. Here, we believe that **listening, collaborating, innovating responsibly, and continuously evolving** are attitudes that take us further. If you seek to join a **collaborative environment that values continuous learning and excellence**, come build this story with us and contribute to delivering greater quality, safety, and care to people's lives. **Hypofarma** **By your side for life.** **Responsibilities and Duties** * Manage the **Pharmaceutical Quality System**, focusing on **Quality Risk Analysis**, ensuring compliance with the **Quality Policy and Good Manufacturing Practices (GMP)**. * Responsible for **leading and supporting risk analyses, investigations of non-conformities, change controls, and internal audits**, as well as **developing and reviewing quality documents**. * Also participate in **continuous improvement projects**, supplier qualification, internal training, and implementation of programs such as the **Contamination Control Strategy (CCS)** and **5S**, contributing to strengthening the quality culture and mitigating process risks. **Requirements and Qualifications** * Bachelor’s degree in **Pharmacy, Chemistry, Chemical Engineering, or related fields**. * Experience in **Quality Assurance** within the pharmaceutical industry. * Solid knowledge of **Quality Risk Analysis (ICH Q9\)** and **Good Manufacturing Practices (GMP)**. * Experience with **deviation investigations, change control, audits, and quality document management**. * Intermediate or advanced Office suite proficiency. * Advanced English proficiency. * **Preferred qualifications:** * Experience with **Contamination Control Strategy (CCS)**. * Experience with **supplier qualification and continuous improvement programs**. **Additional Information** Benefits: Our essence is **care**. Since 1948, we have chosen to stand beside those in need—at every hospital bed, at every step toward well-being. We are part of the health story in Minas Gerais and across Brazil, steadfastly pursuing our strong social purpose. We do not merely deliver medicines—we offer **quality, trust, and dignity**. Every product released to the market carries the rigor of science, the discipline of processes, and continuous innovation. Above all, it embodies **human empathy**, our greatest virtue. **Protecting people** is what drives us. We look toward the future with courage, consistency, and boldness—never forgetting what brought us here: the seriousness of a family dedicated to ensuring the safety and quality required to achieve this goal. Hypofarma’s greatness is measured by every life preserved. It is a calling. It is a commitment. It is our legacy. ***We are by your side for life.*** **Our facilities:** **WE ARE, FIRST AND FOREMOST, PASSIONATE ABOUT WHAT WE DO:**