Description
On behalf of my client, a leader in the medical devices industry, I am currently recruiting a Medical Devices - Regulatory Affairs Manager for a 3-6 month project which should be changed into a permanent assignment after the initial contract period. Therefore, candidates who are willing to take the long term opportunity will be preferred.Your responsibilities will include (not limited to):
*US submissions for manufacturing process
*Advice on regulatory requirements
*Provide RA Strategy
*Perform Product Change Notifications
*RA POC for inspections and readiness programs
*Change management
*Continues RA related process
Requirements:
*Engineering Degree
*At least 5 years of experience in Medical Devices (or other LS industries)
*Expert for Medical Devices submissions knowledge (US Class II/III & EU AIMD)
*Strong Compliance/Quality Systems Regulations
*Fluent in English (French is a significant advantage)
If this role could be of interest for you please reply with your up to date CV including your hourly rate expectation for immediate consideration.