The Principal Regulatory Affairs Specialist will play a critical role in preparing comprehensive regulatory strategies for complex new devices and post market changes within Philips' Ultrasound business. Develop regulatory strategies and communicate risks within regulatory strategies vs project plan...
The position of Regulatory Affairs Specialist II is within our Infectious Disease business unit. Provides regulatory support to regional regulatory teams to assist with submissions, license renewals, and license amendments. Provides regulatory support for diagnostic product development and commercia...
Under limited supervision, the Senior Regulatory Specialist is responsible for planning and executing critical and complex global regulatory projects necessary to obtain and maintain global regulatory approvals. Prepare comprehensive regulatory strategies for new devices, new launch markets, and pos...
Which includes: tracking of status and progress of regulatory documentation, reviewing, editing and proofreading regulatory documentation, participating as an active team member of project teams as required, maintaining regulatory files in a format consistent with requirements as well as staying awa...
Under limited supervision, the Senior Regulatory Specialist is responsible for planning and executing critical and complex global regulatory projects necessary to obtain and maintain global regulatory approvals. Prepare comprehensive regulatory strategies for new devices, new launch markets, and pos...
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 develop Environment, Health, Safety, and Transportation (EHS&T) informa...
The International Regulatory Specialist is responsible for providing regulatory support to Rust-Oleum's international business. Be part of a regulatory team that supports a >. ...
Handling data management and retrieval of regulatory documents. Preparing and submitting US regulatory filings on time and in compliance. Staying current with regulations and providing expertise in regulatory affairs. Training team members and ensuring regulatory compliance. ...
The International Regulatory Specialist is responsible for providing regulatory support to Rust-Oleum’s international business. Be part of a regulatory team that supports a >. ...
Which includes: tracking of status and progress of regulatory documentation, reviewing, editing and proofreading regulatory documentation, participating as an active team member of project teams as required, maintaining regulatory files in a format consistent with requirements as well as staying awa...
Review and process entry of HMDA and CRA reportable loans with 100% accuracy into Compliance CRA Wiz system following current regulatory guidelines. Then preparing a HMDA or CRA packet for all identified loans for regulatory purposes. ...
The International Regulatory Specialist is responsible for providing regulatory support to Rust-Oleum's international business. Be part of a regulatory team that supports a >. ...
Which includes: tracking of status and progress of regulatory documentation, reviewing, editing and proofreading regulatory documentation, participating as an active team member of project teams as required, maintaining regulatory files in a format consistent with requirements as well as staying awa...
Senior Regulatory Affairs Specialist. Participate as the regulatory functional product team member for the organization’s Transfusion Medicine regulatory team. Work with Regulatory and CFT to improve efficiency in regulatory deliverables. Understand, investigate and evaluate regulatory history/backg...
The Principal Regulatory Affairs Specialist will play a critical role in preparing comprehensive regulatory strategies for complex new devices and post market changes within Philips’ Ultrasound business. Develop regulatory strategies and communicate risks within regulatory strategies vs project plan...
Prepares robust regulatory applications (either for FDA or for international regulatory agencies) to achieve departmental and organizational objectives. Acts as core team member providing review and analysis of applicable regulatory guidelines and project regulatory assessments as needed. Reviews an...
The Senior Manager Regulatory Affairs will play a critical role within Philips' Clinical Informatics organization by leading regulatory projects for Philips' Disease Management Solution products, ensuring and maintaining global accurate regulatory strategy and market access, directly impacting the l...
The Senior Manager Regulatory Affairs is the regulatory expert and is responsible for leading the preparation, documentation and submission of regulatory applications for Sysmex products. The Senior Manager position in Regulatory Affairs leads the regulatory strategy for new and modified Sysmex medi...
The Program Manager - Clinical Quality Assurance is primarily responsible for leading the management of GCP quality activities in support of studies and projects across one or more clinical programs to drive proactive quality management, and ensure compliance with corporate policies and functional p...
This individual demonstrates the ability to combine knowledge of scientific, regulatory & business issues to enable development and commercialization of products that are developed, manufactured or distributed to meet relevant US and Canada regulatory requirements. Assures that regulatory strate...
We’re searching for a highly qualified Project Manager to help us maintain our position as an innovative industry authority and ensure that our goals of innovation and outstanding customer service are achieved. Serve as customer advocate on all phases of projects, including planning, schedulin...
Global Regulatory Affairs Strategy roles (U. Responsible for supporting teams & efforts around major filing activities & Regulatory Health Authority (RHA) interactions & meetings, attending & providing regulatory support to other departments, project teams & committees. Assist Re...
The Associate Director, Regulatory Strategic Planning is responsible for successfully delivering project management capabilities for highly complex, cross-functional teams within and across the Regulatory Affairs organization. The individual combines knowledge of scientific, regulatory, and business...
Responsible for a product(s) or products with multiple driver indications within a Therapeutic Area and supports the Manager (Global Regulatory Lead (GRL), Associate Director, or Director), in the development & execution of the regulatory strategy. Assures that regulatory strategies defined with...
As a Regulatory Affairs Manager for my client, you'll play a key part in shaping the future of innovative medical devices. Step into a role where your regulatory expertise will make a global impact. Drive forward the development and compliance of products at the cutting edge of technology, ensur...