RAM - US Submissions

Job type:
on-site
Start:
03/2015
Duration:
6 Months
From:
Real Staffing
Place:
Geneva
Date:
03/06/2015
Country:
flag_no Switzerland

Project description:
Warning
This project is archived and not active any more.
You will find vacant projects in our project database.
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.