Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices,
Who is CorDx？ CorDx a multi-national biotech organization focused on pushing the limits of innovation and supply in global health. With over 2,100 employees across the world, serving millions of users in over 100 countries, CorDx
As a result of the combination of the BD Biosciences and Diagnostic Solutions business with Waters Corporation (NYSE: WAT), by applying to this role, you will be applying for a position with Waters. Waters is a
Company Overview Amperesand is reinventing how the world powers its most critical systems. We are facing a once-in-a-generation opportunity for infrastructure disruption. Electricity demand is skyrocketing, driven by AI factories, electric vehicles, and modern industrial growth.
Join the team leading the next evolution of virtual care. At Teladoc Health, you are empowered to bring your true self to work while helping millions of people live their healthiest lives. Here you will be
Job Description: JOB SUMMARY: Director, Clinical Affairs is a senior-level leadership position that bridges clinical strategy, medical/dental affairs, and regulatory/commercial functions. The Sr. Clinical Research Manager is responsible for defining and executing the overall clinical strategy
Cyber Resilience Act (CRA) Compliance Lead At Altera, our independence as the worlds largest pure-play FPGA solutions provider gives us the focus, speed, and agility to innovate without compromise. With more than four decades of industry-leading
Sr. Regulatory Affairs Specialist 100% ONSITE in Westlake Village, California Sponsorship is not available for this role Caldera Medicals Mission - To Improve the Quality of Life for Women! Message from the Hiring Manager: In your
Regulatory Affairs Specialist The Regulatory Affairs Specialist is responsible for planning, preparing, coordinating, and managing global regulatory submissions and registrations for medical devices, including US 510(k), EU technical documentation, and international dossiers. The role represents Regulatory
Manager, Design Center Join Kyocera International, Inc. Were hiring a Manager, Design Center at our San Diego, CA location! Salary Range: $115,807 $167,684 annually (Final offer based on experience, education, skills, and market factors) With nearly
Senior Project Manager/Clinical Evaluation Reporting Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and
Manager, Quality & Regulatory Compliance Join the team leading the next evolution of virtual care. At Teladoc Health, you are empowered to bring your true self to work while helping millions of people live their healthiest
Senior Technical Program Manager, Compliance Amperesand is reinventing how the world powers its most critical systems. We are facing a once-in-a-generation opportunity for infrastructure disruption. Electricity demand is skyrocketing, driven by AI factories, electric vehicles, and
Director, Clinical Affairs Director, Clinical Affairs is a senior-level leadership position that bridges clinical strategy, medical/dental affairs, and regulatory/commercial functions. The Sr. Clinical Research Manager is responsible for defining and executing the overall clinical strategy in
Jr. Regulatory Affairs Specialist Irvine, CA- (100% onsite) Contract to hire $30- $31.25 an hour Immediate hire for a Jr. Regulatory Affairs Specialist that will support product development teams to deliver regulatory inputs, strategies, reports and
Clinical Affairs Manager Innova Medical Group, Inc. delivers better global health outcomes with its deep expertise in testing and unique offerings in diagnostic medical devices and services that help tackle some of the worlds most challenging
Regulatory Affairs Specialist This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S. and Europe, support of international product registrations and related regulatory affairs activities, including execution
Join Our Regulatory Affairs Team Make a meaningful difference to patients around the world. From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex domestic and international regulatory environments. Working in
Quality Assurance/Regulatory Affairs Specialist Please note this is an in-office position, requiring candidates to be in Irvine, CA. Relocation is not provided for this position. Highly applicable candidates for this role have a background or degree
Job Title Responsibilities: Prioritize and monitor cases throughout the day, provide status updates as necessary. Support the IVDR labeling conversion and revisions of technical files for appropriate products that are due to convert to the new