The Principal Regulatory Affairs Specialist will develop and implement regulatory strategies to obtain timely approvals from regulatory authorities worldwide. The Principal Regulatory Affairs Specialist will understand the regulations governing medical devices and will be responsible for assessing c...
The Principal Regulatory Affairs Specialist will develop and implement regulatory strategies to obtain timely approvals from regulatory authorities worldwide. The Principal Regulatory Affairs Specialist will understand the regulations governing medical devices and will be responsible for assessing c...
The Principal Regulatory Affairs Specialist will develop and implement regulatory strategies to obtain timely approvals from regulatory authorities worldwide. The Principal Regulatory Affairs Specialist will understand the regulations governing medical devices and will be responsible for assessing c...
The Principal Regulatory Affairs Specialist will develop and implement regulatory strategies to obtain timely approvals from regulatory authorities worldwide. The Principal Regulatory Affairs Specialist will understand the regulations governing medical devices and will be responsible for assessing c...
The Senior Regulatory Specialist responsible for Canadian legislation identifies, collects, and interprets science-based reports, data and regulations in order to prepare documents for government agencies, curate lists and/or develop Environment, Health, Safety, and Transportation (EHS&T) inform...
The Principal Regulatory Affairs Specialist will develop and implement regulatory strategies to obtain timely approvals from regulatory authorities worldwide. The Principal Regulatory Affairs Specialist will understand the regulations governing medical devices and will be responsible for assessing c...
The Principal Regulatory Affairs Specialist will develop and implement regulatory strategies to obtain timely approvals from regulatory authorities worldwide. The Principal Regulatory Affairs Specialist will understand the regulations governing medical devices and will be responsible for assessing c...
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...
May review, interpret, and report Regulatory leadership on product specific regulatory issues that may have material impact on the business units, the corporation, or the customer. Interfaces with regulatory authorities on regulatory and technical matters, as appropriate. Manage activities associate...
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...
The Principal Regulatory Affairs Specialist will develop and implement regulatory strategies to obtain timely approvals from regulatory authorities worldwide. The Principal Regulatory Affairs Specialist will understand the regulations governing medical devices and will be responsible for assessing c...
Regulatory Affairs Specialist II. Regulatory Affairs Specialist II:. Regulatory Affairs Specialist II:. Works in close collaboration with internal customers and supports multiple projects to align on regulatory strategy to achieve business objectives. ...
The Principal Regulatory Affairs Specialist will develop and implement regulatory strategies to obtain timely approvals from regulatory authorities worldwide. The Principal Regulatory Affairs Specialist will understand the regulations governing medical devices and will be responsible for assessing c...
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 Compliance Technical Analyst II is responsible for managing and supporting the development, implementation, and maintenance of compliance systems, initiatives, projects, and other key systems and data driven activities within the Compliance department and the organization. Evaluate, design, and ...
Veris Manufacturing, an Emerald Technologies company, has an exciting opportunity for a Program Manager (PM) to join our Brea, CA team! The ideal Program Manager is a self-starting, multifaceted individual who can manage various activities related to the customer and order management experience incl...
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. ...
The Project Success Manager will manage and update project status’ using the CRM, and other Gsuite platforms. They will collaborate closely with the Business Development Managers and the Supply Chain along with other departments for the successful completion of projects and with a goal of incr...
The Senior Project Manager reports to the Director of Project Management and is responsible for directing multiple wet pipeline projects and working closely with other business partners to plan, facilitate and complete projects. The successful candidate will represent the company in communications d...
Since 2000, Clearview Treatment Programs in Los Angeles, CA, has offered individualized evidence-based mental health treatment for adults suffering from mental health disorders, including borderline personality disorder (BPD), and substance use disorders, with an emphasis in dialectical behavior the...
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...
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...
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...
Email Quality Assurance Specialist. Conduct quality assurance reviews and other activities to ensure the accuracy and timeliness of email deployments. ...