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Description: * Must have 1-2 years of experiences in Medical Device Reg Affairs * Have working knowledge in EU MDR Have working knowledge in Regulatory...
* Maintain global establishment & medical device, drug, & cosmetic registrations & listings * Ensure product labeling claims are accurate, substantiated...
Our client, an Innovative Medical Device company, has engaged GForce Life Sciences to provide a Regulatory Specialist. Thisposition will report...
* Support the IVDR labeling conversion and revisions of technical files from the IVD Directive requirements to the new IVD Regulation. * Work cross...
Supply Chain Specialist-Must have experience with Drug Supply Chain Security Act (DSCSA) AREAS OF RESPONSIBILITY * Acquire in-depth knowledge...
DivIHN (pronounced "divine") is a CMMI ML3-certified Technology and Talent solutions firm. Driven by a unique Purpose, Culture, and Value Delivery...
DivIHN (pronounced "divine") is a CMMI ML3-certified Technology and Talent solutions firm. Driven by a unique Purpose, Culture, and Value Delivery...
As an individual contributor, the function of a Regulatory Affairs Specialist is to provide support for the regulatory department to ensure efficient...
Gentiva Hospice is a member of the Gentiva family - an industry leader in hospice, palliative, home health, and personal home care. Our place is...
Gentiva Hospice is a member of the Gentiva family - an industry leader in hospice, palliative, home health, and personal home care. Our place is...
Gentiva Hospice is a member of the Gentiva family - an industry leader in hospice, palliative, home health, and personal home care. Our place is...
Now hiring in New York, New York Kelly Science & Clinical is seeking a Regulatory Affairs Ops Specialist near Round Lake, IL. Long term contract...
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 Newark, New Jersey SummaryOur client, a Fortune 500 Medical Device Company, has engaged GForce Life Sciences to provide a complaint...
Our client, an Innovative Medical Device company, has engaged GForce Life Sciences to provide a Regulatory Specialist. Thisposition will report...
Now hiring in San Diego, California Regulatory Affairs SpecialistSalary Range: $90,000.00 To 110,000.00 Annually About the Opportunity:The...
Now hiring in Sacramento, California Our client, a leader in the pharmaceutical industry, is seeking a Regulatory Information Management Specialist...
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...
he Head of Medical Writing will be responsible for providing leadership and strategic direction to the medical writing function, ensuring the...
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