Description:
* Must have 1-2 years of experiences in Medical Device Reg Affairs
* Have working knowledge in EU MDR Have working knowledge in Regulatory...
As an individual contributor, the function of a Regulatory Affairs Specialist is to provide support for the regulatory department to ensure efficient...
Now hiring in Parsippany, New Jersey SummaryOur client, a Fortune 500 Medical Device Company, has engaged GForce Life Sciences to provide a complaint...
Now hiring in New York, New York Position SummaryThe primary responsibility of the Regulatory Affairs Specialist is to manage and perform regulatory...
Lead Mechanical Engineer opportunity to work for a top 10 premier CDMO. This position is working on a well funded site that will be growing over the...