Senior Quality Control Analyst

Description

Job Summary: Senior Quality Control Analyst responsible for quantitative and qualitative analyses of raw materials and finished products using laboratory equipment. Key Highlights: 1. Responsibility for quantitative and qualitative analyses 2. Use of equipment such as HPLC and UV 3. Development of stability and analytical transfer protocols **Senior Quality Control Analyst** A company's success depends on the passionate people who work there. Together, we share our talents. As one of the leading animal health companies, Ceva Animal Health believes that our success is linked to our passionate people who research, develop, produce, and deliver innovative health solutions for all animals—contributing to the future of our diverse planet. We are committed to ensuring the highest possible level of care and welfare for farm animals (poultry, swine, ruminants), companion animals (dogs and cats), and wildlife. Our vision “Together, Beyond Animal Health” emphasizes that the health and well-being of people, animals, and our planet are fully interconnected. More than ever, Ceva is committed to a “One Health” approach. As part of our “Diversity, Inclusion, and Equity” policy, Ceva Animal Health is committed to the employability of people with disabilities and will make the necessary accommodations during the selection process to ensure inclusion and accessibility for all candidates. To request an accommodation, please contact a member of Ceva’s Human Resources team. **Your Responsibilities:** * Responsibility for organizing primary and secondary standards used in the laboratory’s chemical analyses. * Responsibility for quantitative and qualitative analyses of raw materials and finished products. * Responsibility for operating HPLC, UV, and other equipment. * Responsibility for hosting, conducting, preparing protocols, and reporting on follow-up stability studies. * Responsibility for developing, executing, and reporting on analytical transfer protocols; * Responsibility for developing, executing, and reporting on supplier qualification protocols. **Your Profile:** * Bachelor’s degree completed in Pharmacy, Chemistry, Biochemistry, or Chemical Engineering; * Health regulations and legislation; * Implementation of processes and procedures; * Methodology validations; * Knowledge of GMP; * Operation of HPLC, UV, and other laboratory equipment; * Good laboratory equipment practices and troubleshooting; * Familiarity with pharmacopoeias (United States, European, and Brazilian), IN No. 15 (stability testing of veterinary pharmaceutical products); * Knowledge of 5S systems; * Intermediate English desirable (writing/reading); * Knowledge of KPIs (Key Performance Indicators) for raw materials, products, and stability.