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865 Regulatory Affairs Specialist Jobs Nationwide

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Our client, an Innovative Medical Device company, has engaged GForce Life Sciences to provide a Regulatory Specialist. This position will report...
* Assist with ensuring labeling and directions for use comply with all applicable regulatory requirements * Control labeling and Directions...
* 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...
* Provide administrative support to the Healthcare Regulatory Compliance team including reviewing, updating, and coordinating regulatory...
This is an onsite role, reporting to our Grove Avenue, Indianapolis, IN location daily. About Us Global Preparatory Academy (GPA), is a dual language...
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...
The Senior Regulatory Affairs Specialist will be responsible for performing a wide variety of tasks to ensure global compliance with all cosmetic...
* Manage vendor relationships and deliver on clinical portfolio * Maintain and report on program budgets, such as long-range forecasting and...
The successful candidate will be responsible for supporting regulatory strategy, systems, processes, submissions, and health authority interactions...
* Responsible for liaising with project teams to procure documents necessary for regulatory and ethics committee submissions. * Responsible...
Location: 19 East Chocolate Avenue, Hershey PA, 17033 (Possibility of remote after training with the team) Types of position: Contract Duration...
The Medical Communications Specialist develops, maintains, and applies an appropriate level of disease/therapeutic area/product knowledge...
Acts as technical regulatory lead on core product development teams, communicates regulatory requirements and impact of regulations to project...
* Assist in establishing and maintaining regulatory functions and systems to ensure continuous medical device and environmental regulatory...
Immediate need for Regulatory Affairs Specialist with a Clinical Research Organization in Raleigh. Hybrid position - will work partly in office...
* Manage Corrective and Preventive Actions (CAPA) processes, ensuring timely resolution and documentation. * Handle complaints efficiently...
As a Part-Time Cosmetic Adverse Events Data Entry Specialist, you will play a crucial role in maintaining accurate records of adverse events related...
We are NeuroVasc Technologies! We are committed to being the most dynamic creator of neurovascular devices in the world. We deliver excellence...
* Design, manage, and conduct industrial hygiene field activities related to worker exposures, including, but not limited to, air and noise sampling...
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