334 Regulatory Affairs Specialist Jobs Nationwide

The Regulatory Specialist will be a key member of the Beacon Regulatory and Operations team reporting to the Manager of Regulatory Affairs and...

Description: * Must have 1-2 years of experiences in Medical Device Reg Affairs * Have working knowledge in EU MDR Have working knowledge in Regulatory...

* Assist in establishing and maintaining regulatory functions and systems to ensure continuous medical device and environmental regulatory...

Location: Greensboro, NC - remote to start, but will transition to a hybrid model in the coming months * Contract: 3 month contract to highly likelihood...

Our client, an Innovative Medical Device company, has engaged GForce Life Sciences to provide a Regulatory Specialist. This position will report...

* With minimal supervision, the Regulatory Affairs Expert-Medical Devices manages assigned regulatory tasks related to health authority notifications...

* Responsible for liaising with project teams to procure documents necessary for regulatory and ethics committee submissions. * Responsible...

The Medical Communications Specialist develops, maintains, and applies an appropriate level of disease/therapeutic area/product knowledge...

This is an onsite role, reporting to our Grove Avenue, Indianapolis, IN location daily. About Us Global Preparatory Academy (GPA), is a dual language...

* Design, manage, and conduct industrial hygiene field activities related to worker exposures, including, but not limited to, air and noise sampling...

* Assist with ensuring labeling and directions for use comply with all applicable regulatory requirements * Control labeling and Directions...

Immediate need for Regulatory Affairs Specialist with a Clinical Research Organization in Raleigh. Hybrid position - will work partly in office...

The successful candidate will be responsible for supporting regulatory strategy, systems, processes, submissions, and health authority interactions...

* Prepare and submit regulatory submissions, including 510(k) and MDR, to ensure compliance and support product commercialization. * Collaborate...

Our client, an Innovative Medical Device company, has engaged GForce Life Sciences to provide a Regulatory Specialist. This position will report...

* Coordinates submission and review of documents for inclusion in Design History files. * Drafts, edits and compiles technical documentation...

Work Location is Irvine, CA - Non-Local Candidates, please do not apply. Hybrid Monday-Friday 8am-5pm 3 days on site Tuesday,Thursday and one...

We are NeuroVasc Technologies! We are committed to being the most dynamic creator of neurovascular devices in the world. We deliver excellence...

Our client, an Innovative Medical Device company, has engaged GForce Life Sciences to provide a Regulatory Specialist. This position will report...

Our client, a Fortune-500 Medical Device Company, has requested that we find them a regulatory affairs specialist to provide support and ensure...