Job DescriptionI am collaborating with a leading international Medical Device company who are looking to add a Regulatory Affairs Specialist to their Regulatoryy team to preapre them for the arrival of the new MDR, MDSAP audit programme and FDA inspections. This is an exciting opportunity for an experienced consultant to work for an organisation that is growing rapidly and enabling people around the world improve one of their vital senses.
My client is looking for an individual who has knowledge of post market surveillance aswell as well change management. Someone who is dynamic, agile and dedicated to the task in hand.
-2+ years regulatory affairs experience in Medical Devices (Preferebly class I + IIa)
-Fluency in English, (German Desirable)
-Degree in related field
-PMS and change management
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 - firstname.lastname@example.org
LinkedIn - www.linkedin.com/in/antony-polito-5abab69b