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...
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...
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. ...
Every project we approach is done so in a thoughtful and unique manner with an experienced and knowledgeable project team best fit to that specific and unique project. A minimum of 5 years of experience as a Project Manager supervising project teams. Extensive experience with ground-up commercial pr...
The Program / Project Manager will be assigned to cross-functional projects or to projects where initial requirements will need further elaboration. Experience managing junior project managers to manage smaller aspects of the larger program. Under the leadership of the Senior Manager, Project Manage...
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 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...
Senior Specialist, Clinical Quality Assurance - Hybrid (Los Angeles, California). The Senior Specialist, Clinical Quality ensures GCP compliance with SOPs, ICH and US FDA regulations, guidelines, and clinical study protocols. Maintain and update Clinical Trial Quality Management system. ...
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...
Provide high level strategic and operational regulatory leadership and mentorship on projects including, but not limited to general regulatory strategies, regulatory requirements for clinical studies and marketing approval in domestic and international markets, regulatory strategic development plans...
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...
The new Global Regulatory Affairs Director is a critical hire to this organization leading PMA regulatory negotiations as the FDA point person as well as guiding clinical affairs, quality management, R&D, and all company team leaders toward successful pre-market approval. In collaboration with the V...
As the Regulatory Affairs Director, you will have the opportunity to lead Allogeneic trials – the most innovative in history! This role allows you to bring past Regulatory knowledge to the table, while also be creative in strategic discussions and decisions. Regulatory Affairs experience within a ph...
This position will be reporting into the SVP of Regulatory Affairs and will be supporting Clinical Regulatory and Regulatory CMC functions. Senior Director, Regulatory Affairs (Generalist). Meet is partnering with a late stage pediatric rare disease startup looking for a high-level Regulatory Affair...
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...
Lead project management in support of day-to-day account activities, including but not limited to Client communications, annual strategic planning, resources and budgets, scheduling, tracking and reporting project progress, presentation development, development of creative briefs, status reports and...
The Senior BSA Compliance Analyst performs various quality controls reviews and monitoring pertaining to the Bank Secrecy Act, USA Patriot Act, Anti-Money Laundering Program, OFAC, and Customer Identification Program compliance using industry standard and regulatory guidance to ensure the Bank's com...
The Senior Compliance Analyst will be a member of Via LA’s Global Compliance team and will support the Licensee audit process. The position will be accountable for identifying, preparing, and supporting the execution of license compliance reviews and initiatives within Via LA. This hybrid role repor...
RBW is partnering with an innovative late clinical-stage, oncology Biotech (140 FTE) in their urgent and business-critical search for a new Director/AD, Regulatory Affairs. The client is seeking an autonomous, results-driven candidate who can lead cross-functionally, work well in a multicultural tea...
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; ...
Senior Program Manager - Packaging, Print Strategy, and Planning. As a senior program manager, you will execute projects heavily involved with the Print Expert team, Print Development, Project Producer team, and external packaging cross-functional teams to define the R&D project scope, align on new ...
Email Quality Assurance Specialist. Conduct quality assurance reviews and other activities to ensure the accuracy and timeliness of email deployments. ...
Must be coming from a programming background. ...