Job DescriptionI am collaborating with a leading international health care company who are looking to add a Post Market Surveillance Specialist to their Quality team to prepare them for the arrival of the new MDR. This is an exciting opportunity for an experienced consultant to work for an organisation who creates tools, technologies, and processes to help researchers and pharmaceutical companies to bring new therapies into worldwide clinical use.
My client is looking for an individual to come in and aid the quality manager in coordinating and implementing PMS procedures and reports. The right individual for this role will have extensive experience in PMS for different classes of medical devices.
-5+ years PMS experience
-Fluency in English, writing and speaking (French Desirable)
-Degree in related field
-Knowledge of global medical device regulations regarding post-market surveillance is preferred (MDD Medical Device Directive & revisions, FDA MDR requirements, etc.)
-Strong communication skills
If this role is of interest to you and you would like to learn more please contact me:
Tel - 41 76 518 05 54
Email - email@example.com
LinkedIn - www.linkedin.com/in/antony-polito-5abab69b