Regulatory Affairs Specialist Jobs in USA

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Advanced Regulatory Affairs Specialist

Bio-techne

profile Minneapolis - USA

By joining Bio-Techne youll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne and all of its brands provides tools for researchers to further treat and prevent disease worldwide.Pay Range:$62300.00 - $102350.00...

30+ days ago
Full Time

Inmate Affairs Specialist

State Of Maryland

profile Baltimore - USA

IntroductionIf you are looking for an exciting career with great benefits pension generous leave competitive salary and the opportunity for advancement and professional growth apply to join the DPSCS team today!The Department of Public Safety and Correctional Services (DPSCS) is seeking dedicated ca...

30+ days ago
Full Time

Senior Regulatory Affairs Specialist (monarch) Med...

Johnson & Johnson

profile Santa Clara County - USA

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 unique...

30+ days ago
Full Time

Manager I, Regulatory Affairs Strategy

Alcon Research

profile Fort Worth - USA

At Alcon were passionate about enhancing sight and helping people see brilliantly. With more than 25000 associates we innovate fearlessly champion progress and act swiftly to impact global eye health. We foster an inclusive culture recognizing your contributions and offering opportunities to grow yo...

30+ days ago
Full Time

Senior Regulatory Affairs Program Lead (monarch) M...

6267-auris Health Legal Entity

profile Santa Clara County - USA

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 unique...

30+ days ago
Full Time

Senior Regulatory Affairs Program Lead (monarch) M...

Johnson & Johnson

profile Santa Clara County - USA

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 unique...

30+ days ago
Full Time

Senior Associate Regulatory Affairs Submission Man...

Abbvie

profile Florham Park - USA

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...

30+ days ago
Full Time

Senior Associate Regulatory Affairs Submission Man...

Abbvie

profile North Chicago - USA

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...

30+ days ago
Full Time

Senior Associate Regulatory Affairs Submission Man...

Abbvie

profile Irvine - USA

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...

30+ days ago
Full Time

Associate, Regulatory Affairs Submission Managemen...

Abbvie

profile North Chicago - USA

The Associate Regulatory Affairs Submission Management manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. With input from the submission teams this individual establishes and maintains submission content planners and associated timelines...

30+ days ago
Full Time

Regulatory Affairs Specialist

Stryker

profile Portage - USA

Work Flexibility: HybridJoin Stryker as a Regulatory Affairs Specialist in Portage MI supporting Instruments Surgical Technologies. This role will support regulatory activities for the Neptune Waste Management System ensuring continued market access compliance and lifecycle management across global...

30+ days ago
Full Time

Regulatory Affairs Specialist On-site

Medtronic

profile Lafayette - USA

We anticipate the application window for this opening will close on - 20 Jun 2026At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. Youll lead with purpose breaking down barriers to innovation in a more connected c...

30+ days ago
Full Time

Research Regulatory Affairs Speciallist

Florida Cancer Specialists & Research Institute

profile Fort Myers - USA

Date Posted:Country:United States of AmericaLocation:Broadway OfficeWHY JOIN FCS At Florida Cancer Specialists & Research Institute we believe our people are our strength and we invest in addition to having a positive impact on the people and communities we serve associates benefit from significant...

30+ days ago
Full Time

Regulatory Affairs Consultant (analyst)

Portland General Electric Company

profile Portland - USA

At PGE our work involves dreaming about planning for and realizing a smarter cleaner more enduring Oregon neighborhood. Its core to our DNA and we havent stopped since we started in 1888. We energize lives strengthen communities and drive advancements in energy that promote social economic and envir...

30+ days ago
Contract

Senior Director Us Regulatory Affairs

Gsk

profile Warren - USA

Welcome to Haleon. Were a purpose-driven world-class consumer company putting everyday health in the hands of just three years since our launch weve grown evolved and are now entering an exciting new chapter one filled with bold ambitions and enormous opportunity.Our trusted portfolio of brands i...

30+ days ago
Full Time

Senior Director Us Regulatory Affairs

Gsk

profile Warren - USA

Welcome to Haleon. Were a purpose-driven world-class consumer company putting everyday health in the hands of just three years since our launch weve grown evolved and are now entering an exciting new chapter one filled with bold ambitions and enormous opportunity.Our trusted portfolio of brands i...

30+ days ago
Full Time

Postal Affairs Specialist

Rr Donnelley

profile Elk Grove Village - USA

The Postal Affairs Specialist is responsible administrative functions related to completion of postal paperworkthe processing and verification of mail and mail related operations. Point of contact for all mattersregarding the United States Postal Service according to Post Printing Quality System Pro...

30+ days ago
Remote

Senior Manager Regulatory Affairs Us Advertising A...

Abbvie

profile Irvine - USA

The Senior Manager Regulatory Affairs US Advertising and Promotion US Specialty combines knowledge of scientific regulatory and business issues to enable products that are developed manufactured or distributed to meet the required legislation. Additionally the individual develops and supervises reg...

30+ days ago
Full Time

Senior Manager Regulatory Affairs Us Advertising A...

Abbvie

profile Florham Park - USA

The Senior Manager Regulatory Affairs US Advertising and Promotion US Specialty combines knowledge of scientific regulatory and business issues to enable products that are developed manufactured or distributed to meet the required legislation. Additionally the individual develops and supervises reg...

30+ days ago
Full Time

Senior Regulatory Affairs Specialist

Cochlear

profile Lone Tree - USA

Change peoples lives and love what you do! Cochlear is the most recognized brand in hearing health care.Senior Regulatory Affairs SpecialistPosition Spotlight:Whatyoullneed:Minimum5 years of regulatory experience and a strong background in FDA submission writingWhatyoulldo: Help to develop support a...

30+ days ago
Full Time