The DBS Core is comprised of an Associate Director, Project Manager, Coordinator, and Regulatory Specialist. Submit regulatory paperwork for outreach-related databases and activities. Provide guidance and direction to team in order to ensure regulatory compliance. ...
A company is looking for a Regulatory Compliance Specialist 4 to support and implement audit programs for cloud infrastructure. ...
In close partnership with the Program Manager(s) (PM), the Regulatory Specialist (RS) facilitates the compliant execution of clinical trials, and assists in the development and maintenance of regulatory documents and standards within the group. This includes: creating and maintaining regulatory docu...
A company is looking for a Regulatory Affairs Specialist to support US and OUS regulatory activities for Class II and III products. CFR 820, MDR)Experience in regulatory affairs, clinical affairs, Quality, or Engineering is required. ...
Find your place at Pace® Join us as a Regulatory Analyst, where you’ll put your love of science to work in the Scientific Insourcing Services department. This candidate will work with vendors to seek out chemical information in an entry-level regulatory services position. ...
Perform assigned regulatory activities including. Assist in strategy implementation and operations for regulatory affairs activities, including development of EU MDR Technical File submissions and responses to Notified Bodies. Assist in maintaining Regulatory records and files. Work Experience Requi...
Entry Level Chemical Regulatory Specialist (Remote). Find your place at Pace Join us as a Regulatory Analyst, where you'll put your love of science to work in the Scientific Insourcing Services department. This candidate will work with vendors to seek out chemical information in an entry-level regul...
Find your place at Pace® Join us as a Regulatory Analyst, where you’ll put your love of science to work in the Scientific Insourcing Services department. This candidate will work with vendors to seek out chemical information in an entry-level regulatory services position. ...
Find your place at Pace® Join us as a Regulatory Analyst, where you’ll put your love of science to work in the Scientific Insourcing Services department. This candidate will work with vendors to seek out chemical information in an entry-level regulatory services position. ...
We are currently hiring a **Regulatory Affairs Operations Specialist I** to work on-site at our St. This new team member will perform specialized level work assignments and/or analyses, evaluation, preparation, and submission of documentation for the worldwide regulatory registration, ensuring produ...
The Regulatory Associate is responsible for activities which lead, improve and drive efficiencies across regulatory product approval processes. Actively participate in various Quality System Community of Practice teams representing Regulatory Affairs interests, assessing impact, and bringing awarene...
Senior Regulatory Affairs Specialist – Structural Heart (on-site) page is loaded Senior Regulatory Affairs Specialist – Structural Heart (on-site) Apply locations United States - Minnesota - St. Senior Regulatory Affairs Specialist. Assist in the development of regional regulatory strategy and updat...
The Regulatory Associate is responsible for activities which lead, improve and drive efficiencies across regulatory product approval processes. Actively participate in various Quality System Community of Practice teams representing Regulatory Affairs interests, assessing impact, and bringing awarene...
Remote-Medical Device Regulatory Affairs Specialist II . As a Regulatory Affairs Specialist II you will:. Work with the international regulatory affairs group to ensure products are registered globally based on the spinoff strategy. Field requests from global regulatory associates for registrations,...
Senior Regulatory Affairs Specialist. Understand, investigate and evaluate regulatory history/background of class, disease/therapeutic context in order to assess regulatory implications for approval. This new team member will provide support for the regulatory department to ensure efficient and comp...
Regulatory Affairs Operations Specialist I. This new team member will perform 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 specifi...
The Regulatory Associate is responsible for activities which lead, improve and drive efficiencies across regulatory product approval processes. Actively participate in various Quality System Community of Practice teams representing Regulatory Affairs interests, assessing impact, and bringing awarene...
Develops domestic and international strategies for regulatory approval of Class II and III electronic medical equipment devices. Coordinates, compiles, and submits US and EU regulatory filings for new and modified products, including PMAs, PMA Supplements, pre-submissions, IDEs, 510(k)s, PMA & I...
In this regulatory affairs specialist position, you will have the opportunity to participate in a global healthcare spin off and act as a contributing member for one of the regulatory affairs teams at the division level. The position will work with the international regulatory affairs group to ensur...
Develops domestic and international strategies for regulatory approval of Class II and III electronic medical equipment devices. Coordinates, compiles, and submits US and EU regulatory filings for new and modified products, including PMAs, PMA Supplements, pre-submissions, IDEs, 510(k)s, PMA & I...
Remote-Medical Device Regulatory Affairs Specialist II . As a Regulatory Affairs Specialist II you will:. Work with the international regulatory affairs group to ensure products are registered globally based on the spinoff strategy. Field requests from global regulatory associates for registrations,...
Remote-Spanish-Speaking-Medical Device Regulatory Affairs Specialist II. As a Regulatory Affairs Specialist II you will:. Work with the international regulatory affairs group to ensure products are registered globally based on the spinoff strategy. Field requests from global regulatory associates fo...
Principal Regulatory Affairs Specialist - Electrophysiology Pulsed Field Ablation. Develops domestic and international strategies for regulatory approval of Class II and III electronic medical equipment devices. Coordinates, compiles, and submits US and EU regulatory filings for new and modified pro...
Remote-Medical Device Regulatory Affairs Specialist II. ...
Remote-Medical Device Regulatory Affairs Specialist II . As a Regulatory Affairs Specialist II you will:. Work with the international regulatory affairs group to ensure products are registered globally based on the spinoff strategy. Field requests from global regulatory associates for registrations,...