Regulatory Affairs Associate

About the RoleCollabera is seeking a skilled Regulatory Affairs Specialist II to join our team. As a key member of our Infectious Disease business unit, you will play a crucial role in preparing documentation for EU Technical Files and international product registrations.

Job OverviewThis role is an exciting opportunity to join our team as a Regulatory Affairs Specialist II.As a key member of our Infectious Disease business unit, you will be responsible for preparing documentation for EU Technical Files and international product registrations.

We are seeking a highly skilled Regulatory Affairs Expert to join our team at Collabera, a Global Digital Solutions Company.Job OverviewCollabera is a leading provider of Software Engineering Solutions for the world's most tech-forward organizations in areas such as Engineering, Cloud, and Data/AI. With operations across 60 locations in 11 countries, we...

Description Schedule :Monday - Friday (40 hrs/wk)8:00 AM - 5:00 PM Department: Corp Compliance Office - 241 Primary Purpose : The Regulatory Affairs Coordinator is a member of the Corporate Compliance office and supports the Public Health Reporting team and Compliance Manager. The Regulatory Affairs Coordinator ensures compliance to new and existing...

Your work will change lives. Including your own. The Impact You’ll Make Recursion is at the forefront of reimagining drug discovery and development through broadening the funnel of potential targets, using technology and standardization to build connected data, and superlinearly scaling our efforts to accelerate the delivery of high-potential drug...

Your work will change lives. Including your own. The Impact You’ll Make Recursion is at the forefront of reimagining drug discovery and development through broadening the funnel of potential targets, using technology and standardization to build connected data, and superlinearly scaling our efforts to accelerate the delivery of high-potential drug...

Job DescriptionJob Description·         The position of Regulatory Affairs Specialist II is within our Infectious Disease business unit.  ·         In this role you will prepare documentation for EU Technical Files and international product registrations.  ·         This job description will be reviewed periodically and is...

Responsible for filing necessary applications and handling all government interactions pertaining to the regulation process for products requiring governmental approval. Authoring and submitting PMA supplements (30-day Notice, Real-Time Reviews, 180-Day Supplements, Annual Reports). Review/approval of engineering study protocols/reports and validation study...

Description Schedule :Monday - Friday (40 hrs/wk)8:00 AM - 5:00 PM Department: Quality Systems & Support - 252 Primary Purpose : The Quality and Regulatory Affairs Specialist I monitors and coordinates organization-wide compliance to current requirements of all quality related regulatory, certifying, licensing, and accrediting agencies. The Quality and...

Job OverviewWe are seeking a skilled Medical Records Supervisor to join our team at the Department of Veterans Affairs. In this role, you will be responsible for overseeing the medical records department and ensuring that all medical information is accurately maintained and up-to-date.Estimated Salary: $65,000 - $85,000 per yearJob DescriptionThe ideal...

About PSG Global Solutions CareersWe are a leading clinical development company with 20+ years of experience in clinical research and strategic resourcing.

This position can be remote for the right candidate who meets desired qualifications.Job OverviewPlan, prepare and review all aspects of ongoing and new regulatory submissions, both U.S. (e.g., PMA, IDE, 510(k), PMA Annual Reports, etc.), and international (e.g., CE Technical Files, Design Dossiers, APAC, etc.). Provide regular status updates and activity...

About Abbott LaboratoriesAs a global healthcare leader, Abbott Laboratories helps people live more fully at all stages of life. Our diverse portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals, and branded generic medicines.We have 114,000 colleagues...

Pacific University achieves excellence and distinction by investing in exceptional people to think, care, create, and pursue justice in our world. We embrace discovery in a close nurturing environment that leads to genuine transformation. Our community is diverse, sustainable, and dedicated to discovery and excellence in teaching, scholarship and...

MAIN JOB RESPONSIBILITIES•Assist current regulatory staff with FDA and international regulatory submissions including 510(k), PMA, design dossiers, technical files, and other registrations, as needed for Class I, II and III medical devices. This may include:o Coordination of essential documents/tools for regulatory submissions (i.e. prepare the required...

About Grainger BusinessesGrainger Businesses, a leading industrial distributor, serves over 4.5 million customers worldwide with products delivered through innovative technology and deep customer relationships.CompensationThis hourly position offers a competitive salary between $24.37 and $36.53, with the actual pay range depending on experience,...

Changing lives. Building Careers. Joining us is a chance for you to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, more than 4,000 of us are challenging what’s possible and making headway to help improve outcomes. The Senior Specialist,...

Changing lives. Building Careers. Joining us is a chance for you to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, more than 4,000 of us are challenging whats possible and making headway to help improve outcomes. The Senior Specialist, Regulatory...

OverviewAbbott Laboratories 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, nutritionals and branded generic medicines.We have an opportunity for a Global Product Lead for...

The OpportunityAbbott is seeking a skilled Global Product Manager to lead the Respiratory Rapid Diagnostics portfolio.This role involves overseeing marketing activities for the assigned product line(s) or business(es), including strategy development, execution, and analysis to achieve business plan objectives and goals.Key ResponsibilitiesDevelop and execute...