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Jobs Search
Start Date
Immediate
Expiry Date
28 Nov, 25
Salary
97500.0
Posted On
28 Aug, 25
Experience
2 year(s) or above
Remote Job
Yes
Telecommute
Yes
Sponsor Visa
No
Skills
Iso, Medical Device Directive, Medical Devices, Regulations
Industry
Pharmaceuticals
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.