A company is looking for a Regulatory Specialist - Dental Operations. Key Responsibilities:Support external and internal regulatory reporting, surveys, audits and investigations impacting dental operationsMonitor incoming regulations and share regulatory guidance with dental operationsPerform monito...
Regulatory Affairs Specialist will be responsible for assisting and supporting core regulatory affairs activities for the business, in addition to supporting advertising, promotional and standards review. Provide expert regulatory advice during the product design and development phases, ensuring reg...
A company is looking for a Senior Regulatory Affairs Specialist responsible for regulatory activities related to medical devices. ...
This Regulatory Affairs Specialist III - APAC will work out of our Alameda, CA, location in the Diabetes Division. Advises project groups on preliminary or fully assessed regulatory strategies and Implements Division Regulatory Strategy in specific product-related activities. Provides regulatory dir...
A company is looking for a Principal Regulatory Affairs Specialist for Digital Health Apps. ...
Our client has a unique opportunity for a highly skilled Principal Regulatory Specialist to join a growing team working on novel technology in the Neurological/Spine space. Lead regulatory strategy and submissions for Class 2 & 3 products, including PMA and 510(k) applications. Develop and execute r...
Principal Regulatory Affairs Specialist – Heart Failure (on-site) page is loaded Principal Regulatory Affairs Specialist – Heart Failure (on-site) Apply locations United States - California - Pleasanton time type Full time posted on Posted 2 Days Ago job requisition id 31079772 Abbott is a global he...
Provides consultation/advice to regulatory specialist for change control and product development. Provides regulatory direction/interpretation on team activities. Interprets and applies regulatory understanding to support of products and teams. Handles regulatory activities involved in documentation...
Responsible for regulatory activities, including product registrations, regulatory impact assessment, etc. ...
As an individual contributor, the Principal Regulatory Affairs Specialist is responsible for providing regulatory guidance to cross-functional partners, developing global regulatory strategies for new and modified Class III devices and preparing and submitting regulatory submissions in the US, EU an...
Provides consultation/advice to regulatory specialist for change control and product development. Provides regulatory direction/interpretation on team activities. Interprets and applies regulatory understanding to support of products and teams. Handles regulatory activities involved in documentation...
Assist in the preparation of regulatory submissions in support of IVDR implementation of Toxicology and Therapeutic Drug Monitoring Assays. Tasks include:o Organize and assist in the review of materials for inclusion in regulatory submissions both in the EU and worldwide. Support the preparation of ...
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...
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...
As an individual contributor, this position performs specialized level work assignments and/or analyses, evaluation, preparation, and submission of documentation for the worldwide regulatory registration, ensuring products and procedures comply with regulatory agency specifications. Prepares robust ...
Senior International Regulatory Operations Specialist. As an individual contributor, the Senior Specialist will provide support for the regulatory department to ensure efficient and compliant business processes and environment. Assist in the development of regional regulatory strategy and update str...
Provides consultation/advice to regulatory specialist for change control and product development. Exempt/Non Exempt: Non Exempt Years Experience: - years regulatory experience and/or years relevant industrial experience typically with a quality, product-development/support, or scientific affairs fun...
Medical manufacturer is hiring a Regulatory Affairs Specialist on a temporary basis. Previous medical device experience in a Regulatory Affairs capacity . ...
Regulatory Affairs Specialist III - APAC. Advises project groups on preliminary or fully assessed regulatory strategies and implements Division Regulatory Strategy in specific product-related activities. Provides regulatory direction on team activities. Applies basic regulatory understanding to supp...
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. ...
Regulatory Affairs Specialist III - APAC. Advises project groups on preliminary or fully assessed regulatory strategies and Implements Division Regulatory Strategy in specific product-related activities. Provides regulatory direction on team activities. Applies basic regulatory understanding to supp...
JCW is working on an exciting search for Regulatory Affairs Specialist III for global Biotech who is expanding their growing team. In this role you will play a key role in planning, managing, and tracking of regulatory submissions and documentation for the production of biological medicines. Account...
Regulatory Compliance Specialist (Customs/Brokerage). Ensure all regulatory communications/updates are received, summarized, catalogued, disseminated and acted upon. Record and maintain all client communication in accordance with company policy and regulatory requirements. ...
Role: Regulatory Specialist II<br /> Location: Alameda,CA- 94502<br /> Duration: 12 Months </div> <div> <div>Job Description </div> <div> <ul> <li> Responsible for regulatory activities, including product registrations, impact assessment, etc....
Job Description: Regulatory Affairs Specialist. Provide consultation and advice to regulatory specialists regarding change control and product development. Ability to interpret and apply regulatory requirements. Offer regulatory direction and interpretation on team activities. ...