ph3About Phibro Animal Health Corporation /h3 pPhibro Animal Health Corporation 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. /p pPhibro 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. /p pAt 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. /p pIf you are interested in working for Phibro and feel that you do not meet all qualifications, we encourage you to apply as you might be the right candidate for this role or other positions. /p pThe QC Supervisor is an integral part of our Quality Control team based out of our Medolla, Italy site. /p h3Position Details /h3 pThis role is responsible for overseeing the laboratory and QC team, planning workload, procedures and testing to ensure acceptable product quality. /p h3Key Responsibilities /h3 ul liResponsible for the laboratory, including stability, retention, safety, cleanliness and order.



/li liSchedules and assigns all activities and ensures they are completed on time. /li liTrains department staff to comply with GMP/GLP regulations and company policies. /li liIn 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. /li liResponsible for assembling the analytical package of batches and delivering it to the site QP for the release of the product batches. /li liIssues analytical certificates of the production batches and submit them to the QP for review. /li liReviews and approvals all documents for release of materials for production use. /li liCheck and control the lab metrics to ensure all KPIs are met. /li liResponsible for writing stability protocols and ensuring that stability tests are performed on time and according to the stability protocol. /li liResponsible for lab investigations and deviations, their execution with the application of the DMAIC method, their opening and management with requested timing. /li liPrepares 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. /li liResponsible 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. /li liSupports the qualification of new materials/suppliers and process validations with analytical tests. /li liResponsible 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. /li liActively participates in external and internal audit. /li liWorks in collaboration with other departments including production, engineering and QA to achieve common site goals. /li liOther duties as assigned. /li /ul h3Key Competencies, Requirements, Complexity /h3 ul liGood knowledge of GMP regulations /li liStrong communication, management and multitasking skills. /li liGood oral and written English. /li liPlanning and organizational skills, including developing successful teams. /li liAbility to independently solve problems. /li /ul h3Education, Knowledge, Year Of Experience /h3 ul liBachelor’s degree in chemistry/biology/chemistry and Pharmaceutical Technologies. /li liAt least 2 years of experience in QC testing including HPLC tests and GC. /li /ul h3Phibro is an Equal Opportunity Employer /h3 pAll 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. /p h3Business Unit: Animal Health Mineral Nutrition /h3 h3Division: Animal Health Nutrition /h3 h3Department: Quality Control /h3 h3Location: Medolla, Italy /h3 h3Work Schedule: Monday - Friday (40 Hours) /h3 /p #J-18808-Ljbffr

📌 QC Supervisor (Medolla)
🏢 Phibro Animal Health
📍 Medolla