The Director Regulatory Affairs Global Regulatory Lead, Global Regulatory Strategy, is responsible for developing and implementing global strategies to secure and maintain market approval for product(s) in the assigned therapeutic area. May lead the Labeling Regulatory Strategy Team (LRST), and serv...
If the answers to these questions were yes; then this Director Quality Assurance and Regulatory Affairs opportunity with an outstanding Medical Device organisation in Illinois might be the change you need. Ensures compliance with regulatory standards and readiness for inspections. Independently revi...
This role will provide CMC regulatory support and guidance for assigned projects and interfaces with R&D, Project Management, Manufacturing, Quality, and Regulatory colleagues to ensure a robust CMC regulatory strategy is developed and implemented to have on time submissions with the highest quality...
Director Regulatory Affairs, Global Regulatory Strategy. Director Regulatory Affairs, Global Regulatory Strategy. ...
The Director Regulatory Affairs Global Regulatory Lead, Global Regulatory Strategy, is responsible for developing and implementing global strategies to secure and maintain market approval for product(s) in the assigned therapeutic area. May lead the Labeling Regulatory Strategy Team (LRST), and serv...
The Director of Regulatory Affairs & Quality will lead the Philips RespirTech InCourage Vest Therapy Regulatory Affairs and Quality teams in the development and execution of compliant regulatory strategies and quality team/QMS responsibilities. Leading Regulatory Affairs strategy end-to-end executio...
The Director Regulatory Affairs, Strategic Labeling is responsible for setting strategy and leading cross-functional, multidisciplinary, therapeutic teams, and executing multidivisional initiatives for labeling activities for drugs, devices and combination products in assigned therapeutic area(s). E...
This role will provide CMC regulatory support and guidance for assigned projects and interfaces with R&D, Project Management, Manufacturing, Quality, and Regulatory colleagues to ensure a robust CMC regulatory strategy is developed and implemented to have on time submissions with the highest qua...
This role will provide CMC regulatory support and guidance for assigned projects and interfaces with R&D, Project Management, Manufacturing, Quality, and Regulatory colleagues to ensure a robust CMC regulatory strategy is developed and implemented to have on time submissions with the highest quality...
The Director, Abbott Nutrition Regulatory Affairs is responsible for combining scientific, regulatory, and business knowledge to ensure our nutritional product portfolio in LATAM meets the necessary regulatory requirements, products are approved for placement on market, and that registrations are ma...
This role will provide CMC regulatory support and guidance for assigned projects and interfaces with R&D, Project Management, Manufacturing, Quality, and Regulatory colleagues to ensure a robust CMC regulatory strategy is developed and implemented to have on time submissions with the highest quality...
The Director Regulatory Affairs, Strategic Labeling is responsible for setting strategy and leading cross-functional, multidisciplinary, therapeutic teams, and executing multidivisional initiatives for labeling activities for drugs, devices and combination products in assigned therapeutic area(s). E...
As the Senior Director Regulatory Affairs, Advanced Surgery you will be responsible for global strategic direction and performance (strategy and execution) of the Regulatory Affairs (RA) function within the division including development, implementation and management of global regulatory strategies...
The Enterprise Program Manager will develop, lead (directly or indirectly) a staff of Program Managers and/or Project Coordinators accountable for the planning, directing, and execution of local and/or global development projects. Are you ready to make your mark? If you're an Enterprise Program Mana...
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 Associate, Regulatory Affairs Submission Management, manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. ...
Senior Manager Medical Affairs Quality Assurance is responsible for providing independent quality oversight of GxP activities executed by AbbVies Medical Affairs enterprise, including but not limited to non-interventional studies, medical information and other regulatory commitments. Partner with Me...
We are seeking an experienced SAP Cutover Project Manager to join the SAP Unify Program for a leading healthcare manufacturer client. Minimum of 8+ years of SAP project management experience, ideally 10+ years of project management experience (PMP Preferred). Oversee the full lifecycle of SAP S/4HAN...
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...
Project Manager with proven project. Collaborate with Sales team throughout the bidding process and create project outcome projection. You proudly manage Commercial HVAC projects and lead professional teams to success. You plan and present high-quality projects to valued clients and see them through...
For each project, they implement professional project management processes and project controls to safely deliver to client's construction projects. Project Managers proactively implement project controls with early warning systems to catch potential issues. As a Project Manager, you will play a cru...
Are you ready to lead regulatory strategies that will have a global impact? Join my client as a Senior Manager in Regulatory Affairs, where youll be at the forefront of innovation in the medical device industry. Manage and mentor a team of regulatory affairs professionals. Lead and shape regulatory ...
Represents Global Regulatory Affairs at research and development meetings and presents agreed upon regulatory positions. Follows scientific arguments, identifies regulatory scientific data needs and regulatory issues with alignment of regulatory management. Provides regulatory support and guidance a...
The Associate, Regulatory Affairs Submission Management, manages low to medium-impact submission projects involving multiple cross-functional regulatory submission teams. Job Title: Associate Regulatory Affairs Submission Management. With input from the submission teams, this individual establishes ...
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...