Senior Quality Control Analyst

Description

Job Summary: Senior Quality Control Analyst responsible for chemical analyses, stability studies, technology transfers, and qualifications in animal health. Key Highlights: 1. Responsibility for quantitative and qualitative analyses of raw materials 2. Use of HPLC and UV equipment in laboratory analyses 3. Development of stability and transfer protocols and reports **Senior Quality Control Analyst** A company’s success depends on the passionate people who work within it. 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 production animals (poultry, swine, ruminants), companion animals (dogs and cats), and wildlife. Our vision “Together, Beyond Animal Health” emphasizes that human health, animal health, and planetary health 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 employing persons with disabilities and will make necessary accommodations during the selection process to ensure inclusion and accessibility for all candidates. To request an accommodation, please contact a Ceva Human Resources representative. **Your Responsibilities:** * Responsibility for organizing primary and secondary standards used in laboratory 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, documenting, and reporting follow-up stability studies. * Responsibility for developing, executing, and reporting analytical transfer protocols; * Responsibility for developing, executing, and reporting supplier qualification protocols. **Your Profile:** * Bachelor’s degree in Pharmacy, Chemistry, Biochemistry, or Chemical Engineering; * Knowledge of health regulations and legislation; * Implementation of processes and procedures; * Methodology validations; * Knowledge of GMP (Good Manufacturing Practices); * Hands-on experience with HPLC, UV, and other laboratory equipment; * Good laboratory equipment practices and troubleshooting skills; * Familiarity with pharmacopoeias (United States, European, and Brazilian), IN No. 15 (stability testing of veterinary pharmaceutical products); * Knowledge of 5S systems; * Intermediate English (writing/reading) preferred; * Knowledge of KPIs (Key Performance Indicators) for raw materials, products, and stability.