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...
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...
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...
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 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...
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 Clinical Trial Regulatory Specialist I (CTRS-I) is a novice level position which, under the direction of the KPNC Clinical Trials Compliance Director or designee and Principal Investigator (PI), provides regulatory document support to the Kaiser Permanente Northern California (KPNC) PI and resea...
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...
The IT Project Manager will be responsible for managing assigned resources, creating and tracking detailed project plans, effectively leading and facilitating project meetings, as well as proactively controlling project scope, risks and issues. As the IT Project Manager, you will be part of the Proj...
Cybersecurity & Compliance Analyst (CMMC). Five or more years' experience working in Information Security or Cybersecurity Analyst role with a strong focus on compliance and auditing. Assists in planning, implementing, upgrading, and monitoring security measures and compliance for the protection of ...
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...
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; ...
Our Client - a prominent on demand cloud computing provider-- is looking for a Marketing Program Manager that will oversee generative AI brand awareness marketing programs! You will oversee stakeholder requirements, timelines, and critical meetings. Marketing Program Manager (Los Angeles, CA). This ...
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...
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...
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,...
The QA Specialist is responsible for ensuring that quality requirements are established and maintained in accordance with the appropriate regulations and cGMP guidelines. Write and revise SOPs related to Quality Assurance. This role is to act as a quality liaison to other departments within the comp...
Email Quality Assurance Specialist. Conduct quality assurance reviews and other activities to ensure the accuracy and timeliness of email deployments. ...
Manager of Regulatory Affairs to play a part in their early and late stage clinical trials. Provide leadership to the regulatory therapy area team. Manage regulatory interface with domestic and international health authorities. Develop and deploy regulatory programs for product approval. ...
A growing immuno-oncology company is seeking a Senior/Executive Director of Regulatory Affairs to join the team in executing regulatory strategies and supporting the development of their product pipeline with an emphasis on early stage development. Senior/Executive Director Regulatory Affairs. The S...
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...
Bay Area Senior Manager/Associate Director Regulatory Affairs Opportunity. One of our key mid-sized biotech clients is seeking a dynamic Senior Manager/Associate Director of Regulatory Affairs to become an integral part of their team. This pivotal role will have you steering regulatory strategies in...