WHY JOIN BRACCO MEDICAL TECHNOLOGIES?

We care as much about our employees as we do our patients. Our culture fosters a work environment where employees can thrive, be passionate and have fun along the way. Each member of the Bracco Medical Technologies team has the power to make a difference……every day!
As a Post Market Surveillance Specialist II , you will perform product complaint and post-market surveillance activities on a global basis for ACIST products. You will ensure compliance with global standards and regulations including but not limited to: FDA’s Quality System Regulations (21 CFR 820), ISO 13485, Medical Device Directive (93/42/EEC), the Canadian Medical Device Regulations, Brazil’s Resolution RDC No. 59, China SFDA Regulations for the Supervision and Administration of Medical Devices, Japan’s Ministerial Ordinance 169, and Korea’s Medical Device Regulation.