Regulatory Affairs Intern Jobs in USA

Duration: 12 Months Contract (Extension Possible)Description:Responsible for strategic oversight of safety related labeling variations impacting regulated pharmaceutical drug products while ensuring regulatory compliance patient safety and consistent communication of product information across globa...

Job DescriptionRegulatory Affairs Intern opportunity is open UAE NationalsDuration: 4-8 WeeksLocation: Dubai United Arab EmiratesOur company is committed to developing local talent and supporting the next generation of healthcare professionals in the UAE. As a Regulatory Affairs Intern you will gain...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquel...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquel...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquel...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquel...

The Regulatory Affairs Specialist supports chemical and product regulatory compliance in the United States. The role coordinates TSCA compliance supports new chemical submissions and reporting evaluates emerging federal and state requirements and provides practical regulatory guidance to internal st...

The Senior Associate Regulatory Affairs Submission Management manages medium to high impact moderately complex submission projects involving multiple cross-functional regulatory submission teams. With input from the submission teams this individual establishes and maintains submission content planne...

The Manager Regulatory Affairs Global Regulatory Strategy US & Canada is responsible for the development and implementation of US and Canada regulatory strategic and tactical planning (RSTP) for assigned on market products or those products in development.This individual assists Regulatory Staff by...

We anticipate the application window for this opening will close on - 3 Nov 2026Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain restore health and extend life. Our 95000 employees work across more than 150 countries to put...

Enter Job Description... Develops and implements programs and processes to ensure that company products are safe legal and meet or exceed customer expectations for compliance with national/regional/global regulations. Regulatory support for integration activities including reviews of product labelin...

Duration: 12 monthsPosition SummaryThe Regulatory Affairs Specialist II will draft assemble and file original documentation and submission materials for new or existing products to regulatory authorities to assure that all submissions are accurate of high quality and well supported by literature and...

Responsible for technical support and product testing in the US with the objective to support sales and operations in growing the business. Primary focus on laboratory testing and regulatory compliance.Job FunctionsProvide technical support to sales teams and account managers internally and/or durin...

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...

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 nutritionals and branded generic medicines. Our 122000 collea...

Job Title -Regulatory Affairs Specialist IIILocation -Bridgewater NJDuration - 9 MonthsJob DescriptionManager will consider candidates to be based in either Bridgewater New Jersey or Cambridge Massachusetts. Please specify on resume which location candidate is being submitted for.Preparing compiling...

Position SummaryThe Sr. Manager Regulatory Affairs for the Digital Portfolio leads regulatory strategy and execution for software-driven products including software as a medical device (SaMD) software in a medical device (SiMD) cloud and connected applications data and analytics tools and AI/ML-enab...

The Associate Director Regulatory Affairs US Advertising and Promotion - Immunology is responsible for setting strategy and leading cross-functional multidisciplinary therapeutic teams and executes multidivisional initiatives. The Associate Director envisions the future by using global marketplace t...

The Associate Director Regulatory Affairs US Advertising and Promotion - Immunology is responsible for setting strategy and leading cross-functional multidisciplinary therapeutic teams and executes multidivisional initiatives. The Associate Director envisions the future by using global marketplace t...

The Associate Director Regulatory Affairs US Advertising and Promotion - Immunology is responsible for setting strategy and leading cross-functional multidisciplinary therapeutic teams and executes multidivisional initiatives. The Associate Director envisions the future by using global marketplace t...