Quality and Regulatory Managers @ Gsap - July 201918 July 2019
We are looking for a Medical Devices QA & RA Managers.
Management of the quality system according to the requirements of ISO 13485: 2016, 21CFR820, MDR.
Communication with the regulatory authorities.
Biotechnology Engineer / Electronics Engineer / Chemistry Engineer / Bachelor's degree in science.
Over 3 years of experience in managing quality systems in medical device companies - Class II products.
Certified Quality Engineer CQE / ICQE - a significant advantage.