QC Supervisor

ppSelect how often (in days) to receive an alert: /ppbAbout Phibro Animal Health Corporation /b /ppbPhibro Animal Health Corporation /b is a publicly traded, global organization with a rich history in animal health and nutrition as a manufacturer and marketer of medicated feed additives, vaccines, nutritional specialty products, and mineral nutrition. We strive to be a trusted partner with livestock producers, farmers, veterinarians, and consumers who raise or care for farm and companion animals by providing solutions to help them maintain and enhance the health of their animals. /ppPhibro is a diversified company in manufacturing and marketing products for ethanol performance, microbials for plants, home and industrial applications, and specialty chemicals for various industrial markets.In addition to, Phibro’s revenues are in excess of $1 billion and are supported by over 2,300 employees worldwide. /ppAt Phibro, people are our greatest asset. We strive to develop a diverse workforce that fosters an environment where people feel supported in openly sharing their creativity and skills that allows them to be the most successful that they can be. /ppTheQC Supervisoris an integral part of our Quality Controlteam based out of our Medolla, Italysite. /ppThis role is responsible for overseeing the laboratory and QC team, planning workload, procedures and testing to ensure acceptable product quality. /ph3KEY RESPONSIBILITIES /h3ulliResponsible for the laboratory, including stability, retention, safety, cleanliness and order. /liliSchedules and assigns all activities and ensures they are completed on time. /liliTrains department staff to comply with GMP/GLP regulations and company policies. /liliIn accordance with the current Monographs, examines and reviews the results of the analytical tests of the finished products, ensuring their integrity and compliance with the registered specifications. /liliResponsible for assembling the analytical package of batches and delivering it to the site QP for the release of the product batches. /liliIssues analytical certificates of the production batches and submit them to the QP for review. /liliReviews and approvals all documents for release of materials for production use. /liliCheck and control the lab metrics to ensure all KPIs are met. /liliResponsible for writing stability protocols and ensuring that stability tests are performed on time and according to the stability protocol. /liliResponsible for lab investigations and deviations, their execution with the application of the DMAIC method, their opening and management with requested timing. /liliPrepares and reviews procedures, monographs, analytical methods and ensures that all department GMP documents are updated according to other departments documentations, applicable regulations and company policies. /liliResponsible for the good condition and efficiency of all equipment lab, ensures that all equipment and instruments used for analyses are qualified and within a periodic maintenance plan. /liliSupports the qualification of new materials/suppliers and process validations with analytical tests. /liliResponsible for the evaluation of analytical data, preparation of annual trends and definitely of control limits for key analytical parameters, as part of the preparation of annual product review. /liliActively participates in external and internal audit. /liliWorks in collaboration with other departments including production, engineering and QA to achieve common site goals. /liliOther duties as assigned. /li /ulh3KEY COMPETENCIES, REQUIREMENTS, COMPLEXITY /h3ulliGood knowledge of GMP regulations. /liliStrong communication, management and multitasking skills. /liliGood oral and written English. /liliPlanning and organizational skills, including developing successful teams. /liliAbility to independently solve problems. /li /ulh3EDUCATION, KNOWLEDGE, YEAR OF EXPERIENCE /h3ulliBachelor’s degree in chemistry/biology/chemistry and Pharmaceutical Technologies. /liliAt least 2 years of experience in QC testing including HPLC tests and GC. /li /ulpbPhibro is an Equal Opportunity Employer /b /ppAll qualified applicants will receive consideration for employment without regard to race, national origin, gender, age, religion, disability, sexual orientation, gender identity, veteran status, marital status or any other characteristics protected by law. /ppbBusiness Unit:Animal Health Mineral Nutrition /bbr/bDivision:Animal Health Nutrition /bbr/bDepartment:Quality Control /bbr/bLocation:Medolla, Italy /bbr/bWork Schedule:Monday - Friday (40 Hours) /b /p /p #J-18808-Ljbffr