Senior Regulatory Affairs Specialist working independently, is responsible for fulfilling regulatory compliance requirements by applying an understanding of regulatory standards and regulations for medical devices, pharmaceuticals, or biologics. As a Senior Regulatory Affairs Specialist you play a p...
A company is looking for a Regulatory Specialist - Dental Operations. Key Responsibilities:Support external and internal regulatory reporting, surveys, audits and investigations impacting dental operationsMonitor incoming regulations and share regulatory guidance with dental operationsPerform monito...
We are actively seeking a highly skilled Principal Regulatory Affairs Specialist to lead our FDA, Health Canada, and/or EU MDR submissions process. Maintains proficiency in worldwide regulatory requirements; monitors changes in the regulatory landscape and is responsible to communicate these changes...
A company is looking for a Regulatory Affairs Specialist. ...
Director/Principal Specialist, Regulatory Affairs - Permanent - Denver, CO. Proclinical is seeking a Director/Principal Specialist, Regulatory Affairs for a rapidly growing and exciting medical technology company specializing in SaMD with AI/ML with their location in the Denver, CO area. The Directo...
A company is looking for a Senior Regulatory Compliance Specialist. ...
The Regulatory Specialist will be responsible for ensuring that the claims made for our dietary supplement products are substantiated by scientific evidence and comply with regulatory requirements. We are looking for a positive, driven, and detail-oriented Regulatory Specialist to join our growing t...
As a Senior Regulatory Affairs Specialist you play a pivotal role in ensuring regulatory compliance and driving the success of our innovative medical products. Senior Regulatory Affairs Specialist. Represents regulatory on project teams to develop regulatory strategies, including reviewing the vario...
Principal, Regulatory Affairs Specialist. We are actively seeking a highly skilled Principal Regulatory Affairs Specialist to lead our FDA, Health Canada, and/or EU MDR submissions process. Maintains proficiency in worldwide regulatory requirements; monitors changes in the regulatory landscape and i...
Principal, Regulatory Affairs Specialist. We are actively seeking a highly skilled Principal Regulatory Affairs Specialist to lead our FDA, Health Canada, and/or EU MDR submissions process. Maintains proficiency in worldwide regulatory requirements; monitors changes in the regulatory landscape and c...
We are actively seeking a highly skilled Principal Regulatory Affairs Specialist to lead our FDA, Health Canada, and/or EU MDR submissions process. Maintains proficiency in worldwide regulatory requirements; monitors changes in the regulatory landscape and is responsible to communicate these changes...
ERM has an opportunity for an experienced biologist/regulatory specialist to join our thriving global consulting firm as a . Principal Biologist/Regulatory Specialist. Principal Biologist/Regulatory Specialist. Serve as Project Biologist/Regulatory Specialist for environmental impact assessment unde...
Senior Regulatory Affairs Specialist working independently, is responsible for fulfilling regulatory compliance requirements by applying an understanding of regulatory standards and regulations for medical devices, pharmaceuticals, or biologics. As a Senior Regulatory Affairs Specialist, you play a ...
Training on the relevant regulatory requirements can be provided for exceptional candidates with an interest in Regulatory reporting, who can demonstrate excellent performance in their current and previous roles. The Regulatory Reporting function has recently been aligned to Investment Operations wi...
Regulatory & Compliance Specialist. Regulatory & Compliance Specialist in our Raleigh, NC or Denver, CO locations. Responsible for working with Project Managers and project teams to ensure successful project execution and delivery of telecommunications regulatory documents, reviews, and permitting. ...
Environmental Regulatory Specialist. For the Managing Consultant, Environmental Regulatory Specialist (Senior Level) position, we anticipate the annual base pay of $76,000 – $94,860 (USD). Federal Energy Regulatory Commission (FERC). Research, analyze and compile data for permit applications and rep...
You will also be responsible for establishing, monitoring and providing oversight or acting as a liaison for compliance programs, processes and department of insurance examinations, as well as making recommendations to leadership on compliance matters that affect the product portfolio, forms, system...
From these plans, the Project Manager will coordinate internally with Engineering, Development, and Operations to fulfill projects on time and within the project budget. The Project Manager will supervise and schedule execution of projects in coordination with Stems customers. As the Project Manager...
The International Student Advisor and Compliance Specialist is responsible for ensuring F-1 non-immigrant students are compliant with federal regulations and university policies. Proactively assist/advise F-1 international students with maintaining their student status and compliance requirements. C...
Ulteig has an opportunity to hire a Senior Project Manager to work specifically with transportation projects for the various states' Department of Transportation offices, ideally TXDOT, CDOT, SDDOT, or NDDOT. The Senior Project Manager will be responsible for the successful initiation, planning, exe...
To be considered for this positionyou must have previous project management experience in the water and waste-water construction industry. Managing cost and "Work In Progress" projections. Planning and scheduling the project. ...
A company is looking for a Vendor Compliance Senior Specialist in Retail Operations. ...
A company is looking for a Senior Quality Assurance Specialist to support quality assurance initiatives in the clinical research field. ...
A company is looking for a Senior Regulatory Affairs CMC Associate. ...
Key Responsibilities:Focus on clinical regulatory filings and providing strategic and operational leadership on project teamsContribute to IND/CTA and BLA submissions activities for products in developmentDevelop regulatory strategies for assigned programs and communicate with regulatory agenciesReq...