QC Supervisor

About Phibro Animal Health Corporation Phibro 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. Phibro 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. At 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. If 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. The QC Supervisor is an integral part of our Quality Control team based out of our Medolla, Italy site. Position Details This role is responsible for overseeing the laboratory and QC team, planning workload, procedures and testing to ensure acceptable product quality. KEY RESPONSIBILITIES • Responsible for the laboratory, including stability, retention, safety, cleanliness and order.  • Schedules and assigns all activities and ensures they are completed on time.  • Trains department staff to comply with GMP/GLP regulations and company policies.  • In 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.  • Responsible for assembling the analytical package of batches and delivering it to the site QP for the release of the product batches.  • Issues analytical certificates of the production batches and submit them to the QP for review.  • Reviews and approvals all documents for release of materials for production use.  • Check and control the lab metrics to ensure all KPIs are met.  • Responsible for writing stability protocols and ensuring that stability tests are performed on time and according to the stability protocol.  • Responsible for lab investigations and deviations, their execution with the application of the DMAIC     method, their opening and management with requested timing.  • Prepares 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.  • Responsible…