A company is looking for a Senior Regulatory Compliance Specialist to assist with the implementation and maintenance of its Compliance Software Program. ...
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 Senior Regulatory Specialist to support product compliance strategies and ensure regulatory standards are met. ...
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 an Associate Regulatory Operations Specialist (Remote). ...
The Regulatory Compliance Specialist will assist the Director and Accounting team with various reporting and compliance issues, including tracking regulatory reporting requirements and maintaining the database for Visionary’s internal master regulatory schedule. Regulatory Compliance Specialis...
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...
Senior Regulatory Affairs Specialist responsibilities include, but are not limited to, the following:. Under the direction of the Manager, Regulatory Affairs and Quality Assurance, this position in tandem with Senior Management, will assist with ensuring that DPT’s laboratories are compliant with th...
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...
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 Filings Specialist:. Resource will support regulatory filings in both gas and electric in all operating jurisdictions. Project planning, organization, being able to create/foster relationships and maintain cross functional communication with Internal departments such as gas, engineering, ...
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. ...
Regulatory Filings Specialist: Resource will support regulatory filings in both gas and electric in all operating jurisdictions. System One is actively seeking a Regulatory Filings Specialist for a long-term contract hybrid position located in Denver, CO. Project planning, organization, being able ...
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...
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...
As our Associate Program Planning Manager, you will lead a group of Program Planners assigned to the Life Extension 2 program, the future of the FBM program. Associate Program Planning Manager to join our mission on the FBM program. Provide oversight of performance to program budgets and communicati...
The IMA Certificate Compliance (IMACC) team is seeking an Analyst to join our team! This role is responsible for the support of the IMACC Advisors in their essential job responsibilities, the auditing of incoming certificates of insurance, reporting compliance to agents and clients, and calling insu...
Key Responsibilities:Develop and implement regulatory strategies for global medical device clearances and approvalsManage regulatory submissions and communications with FDA and EU notified bodiesProvide regulatory guidance to cross-functional teams throughout the product lifecycleRequired Qualificat...
A company is looking for a Compliance Specialist - Contractor to maintain its compliance programs. Key Responsibilities:Maintain the company's SOC 2 compliance programAssist in the preparation for and execution of SOC 2 auditsSupport the implementation of controls for StateRAMP complianceRequired Qu...
Key Responsibilities:Develop and implement regulatory strategies for global medical device clearances and approvalsManage regulatory submissions and communications with FDA and EU notified bodiesProvide regulatory guidance to cross-functional teams throughout the product lifecycleRequired Qualificat...
We are seeking an experienced Regulatory Affairs Manager to lead our efforts in managing and overseeing regulatory submissions and product registrations across medical devices, pharmaceuticals, and biologics. The ideal candidate will have a strong background in regulatory affairs, a thorough underst...
A company is looking for an Associate Compliance Analyst to contribute to its compliance efforts. ...
A company is looking for a Quality Assurance Manual Specialist to ensure high-quality products through testing and documentation. ...
A company is looking for a Regulatory Affairs Specialist to support US and OUS regulatory activities for Class II and III products. CFR 820, MDR)Experience in regulatory affairs, clinical affairs, Quality, or Engineering is required. ...