This position is responsible for providing guidance on regulatory requirements as well as assisting in regulatory related projects and tasks ensuring compliance with FDA regulations, ISO standards, and other regulatory agencies. Provides guidance on regulatory requirements necessary for strategic an...
The Regulatory Affairs Specialist will assist or lead a variety of regulatory tasks in support of global regulatory strategy, regulatory assessment for modified product, regulatory filing for new/modified product, regulatory operation and processes, post-market surveillance. Perform regulatory asses...
Senior Regulatory Affairs Specialist - (Medical Device) - ONSITE position in. Engage with regulatory authorities and agencies to facilitate product approvals and resolve regulatory issues. If you would like to learn more about this Regulatory Affairs Specialist opportunity, apply directly or reach o...
The Public Policy and Regulatory team exists to further the interests of our community of hosts and guests with politicians, regulators, opinion leaders and others who shape the political and legal context for our business, helping them to understand the significant social and economic contributions...
Our client, a large healthcare company is seeking a Regulatory Affairs Specialist to join their team! As the Regulatory Affairs Specialist you would provide regulatory support and expertise by developing global regulatory strategies, identifying needed registration data, obtaining this data and ensu...
Regulatory Compliance Specialist. Qualifying experience must include reviewing, preparing, and evaluating regulatory permits, and analyzing compliance with regulatory programs. Four (4) years of experience in a regulatory compliance, permit acquisition, occupational health or safety, industrial hygi...
Associate FCP candidates could come from a variety of disciplines which include, Environmental Planners, Biologists, Regulatory Specialists, City Planners, or Archeologists (or many of the other specialties within the CEQA/environmental planning field). Successful candidates will have experience wit...
Represent the regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including presenting alternatives for meeting regulatory requirements and resolving moderately complex conflicts between those requirements and development issues; also keeps...
The Sr Regulatory Affairs Specialist is responsible for ensuring digital medical device regulatory clearance to enable market access by demonstrating compliance to applicable regulations through a registration dossier. Provides regulatory guidance and defines regulatory strategy for digital products...
This position is posted here as a Research Compliance Analyst 3 (job #32758381) and a Research Compliance Analyst 4 (job #32790375). The Research Compliance Analyst will be responsible for providing support and leadership to the Institutional Review Boards (IRBs) as well as providing back up support...
As a Quality Assurance Specialist at Bell Brothers, you will play a crucial role in identifying and qualifying potential customers, driving lead generation, and contributing to the sales pipeline. Achieve productivity standards and goals set by the company while maintaining high-quality calls. ...
Licensing & Compliance Specialist. Licensing & Compliance Specialist. The Licensing and Compliance Specialist plays a critical role in supporting Finance Operations by managing all aspects of business and security agency licensing across the various jurisdictions where the company operates. The Kais...
Moorecroft is looking for that talented Technical Program Manager for a contract role. Working knowledge of modern program management, analysis, tracking, and reporting tools such as Jira/Confluence, Airtable, G-Suite (Google: Docs, Sheets, Slides) , and MS Office. ...
Program Managers are responsible for managing all phases of the program life cycle from inception (proposal development) through startup, execution, and completion (contract closeout). Leading and directing cross-functional Integrated Program Teams (IPT) to meet program cost, schedule, and technical...
Business Intelligence Developer & Analyst - Compliance. Business Intelligence Developer to join our Compliance Operations team to lead compliance focused analytics on multiple campaigns. Fully manage multiple campaigns and clients by serving as the lead for all compliance and operational reporting; ...
Years of experience as Technical Program Manager OR Technical Project Manager (must have managed multiple projects) – leading cross functional teams. Technical Program Manager (AI/ML). ...
Job Opportunity: Senior Project Manager (Construction). PMCS Group is a leading project management consulting firm specializing in capital improvement projects. We are seeking experienced Senior Project Managers (SPM I and SPM II) to join our team. Ideal candidates will have extensive experience in ...
We cross the entire spectrum of business, government, healthcare, education and entertainment and we’re currently seeking an experienced Project Manager to join our team. Ensuring the delivery of the project installation to the customer within the time and budget parameters of the project. Carrying ...
The Project Manager will oversee projects from start-to-finish. This is a full-time, on-site role for a Project Manager at Nadel Architects. Project types include high-end retail, high-end fitness facilities, complete mall repositionings, ground-up development, and market/grocery (boutique and natio...
The Associate Director / Director, Regulatory Affairs will work closely with the Regulatory Affairs team and other departments to develop and implement regulatory strategies for the company's rare disease development programs. Assist in the development and implementation of strategies for early regu...
A growing medical device company based in San Diego county is hiring a Regulatory Affairs Manager for their QA/RA department. The RA Manager will be responsible for leading the regulatory strategy and managing submissions for new product launches. Prepare, review, and submit regulatory documentation...
Email Quality Assurance Specialist. Conduct quality assurance reviews and other activities to ensure the accuracy and timeliness of email deployments. ...
The Senior Specialist, Clinical Quality ensures GCP compliance with standard operating procedures, ICH and US FDA regulations and guidelines, and clinical study protocols. Participate in solving GCP compliance issues within Quality Assurance, Clinical Operations, Regulatory Affairs, Medical Affairs,...
Supports Quality Assurance, and Quality Control activities to ensure operations are conducted in compliance with applicable regulations and standard operating procedures to ensure product quality is consistent with the specifications and facilitate batch disposition for commercial purposes. Supports...
Environmental Permitting and Compliance Specialist). Environmental Permitting and Compliance Specialist). Join Yorke Engineering, LLC, an Environmental Consulting leader in California that implements Environmental Engineering and Compliance solutions for our clients throughout California. Our missio...