Regulatory Affairs Jobs in USA

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Senior Medical Writer

Johnson & Johnson

profile Warsaw - 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...

7 days ago
Full Time

Rems Audit Oversight Lead

Gsk

profile Newark - USA

At GSK we have bold ambitions for patients aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines combining our understanding of the immune system with cutting-edge technology to transform peoples li...

7 days ago
Full Time

Manager, Quality Assurance Operations

Catalent

profile Princeton - USA

Manager Quality Assurance OperationsPosition Summary:Work Schedule: Monday Friday 8:00am-5:00pm. 100% on-site Catalent is a leading global CDMO trusted by pharma biotech and self-care companies to accelerate the development manufacturing and delivery of products that improve lives.With advanced tec...

7 days ago
Full Time

Medical Director, Dermatology – Us Medical Affairs

Johnson & Johnson

profile Horsham - 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...

7 days ago
Full Time

Associate Medical Director, Us Medical Affairs, De...

Johnson & Johnson

profile Horsham - 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...

7 days ago
Full Time

Senior Director, Global Distribution Quality

Ultragenyx Pharmaceutical

profile Bedford - USA

Why Join UsBe a hero for our rare disease patientsAt Ultragenyx we fundamentally believe that taking real impactful action to care for the needs of patients and our people is always the right thing to achieve this goal our vision is to lead the future of rare disease medicine. For us this means goi...

7 days ago
Full Time

Manager, Standards Management (dastfl)

Johnson & Johnson

profile Titusville - 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...

7 days ago
Full Time

Director, Clinical Sciences, Oncology

Johnson & Johnson

profile Spring House - 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...

7 days ago
Full Time

Director, Vitreoretinal Instrumentation Upstream

Alcon Research

profile Fort Worth - USA

At Alcon we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly champion progress and act with speed as the global leader in eye care. Here youll be recognized for your commitment and contributions and see your career like never before. Together we go above and...

7 days ago
Full Time

U.s. Project Licensing Manager

Ge Vernova

profile Washington DC - USA

Job Description SummaryThe U.S. Licensing Manager Regulatory Affairs will lead a licensing team and manage the completion of various regulatory work scopes including new Gen III and Gen IV advanced nuclear power plant licensing operating plant reload licensing customer plant support on GE Hitachi (G...

7 days ago
Full Time

Spec 3, Quality Assurance

Millenniumsoft Inc

profile Irvine - USA

Position : Supplier Quality Analyst Location : Irvine CA Duration : 6 Months Total Hours/week : 40.00 1st Shift Client : Medical Devices Company Job Category : Quality Employment Type : Contract on W2 (Need US Citizens or GC Holders or GC EAD or OPT or EAD or CPT JOB DESCRIPTION Job Summary T...

7 days ago
Full Time

Data Entry Specialist (part-time)

Inx International Ink Co.

profile West Chicago - USA

This role offers a starting range of $21 to $24 per hour. Actual compensation will be based on qualifications such as experience education certifications and skills as well as geographic considerations.We are looking for a Part-Time Data Entry Specialist (up to 24 hours/week) to support our Regulato...

8 days ago
Part-time

Manager, Regulatory Strategic Planning

Abbvie

profile North Chicago - USA

The Manager Regulatory Strategic Planning is responsible for successfully delivering project management capabilities for cross-functional teams of low- to medium-complexity within and across the Regulatory Affairs organization. The individual combines knowledge of scientific regulatory and business...

8 days ago
Full Time

Code Development Architect

City Of New York

profile New York City - USA

The NYC Department of Buildings is responsible for ensuring the safe and lawful use of buildings and properties by enforcing the NYC Construction Codes Energy Code and Zoning Resolution. We facilitate compliant development with integrity efficiency and professionalism. We are committed to becoming t...

8 days ago
Full Time

Regulatory Affairs Analyst

Johnson & Johnson

profile Raynham - 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...

8 days ago
Full Time

Regulatory Affairs Program Manager

Philips

profile Plymouth - USA

Job TitleRegulatory Affairs Program ManagerJob DescriptionRegulatory Affairs Program ManagerIn this role you The Regulatory Affairs Program Manager is responsible to optimize regulatory compliance monitoring and reporting efficiency implementing robust systems and processes to ensure accurate and ti...

8 days ago
Full Time

Sr Regulatory Affairs Manager

Medtronic

profile Lafayette - USA

We anticipate the application window for this opening will close on - 1 May 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 co...

8 days ago
Full Time

Sr Regulatory Affairs Manager

Medtronic

profile Lafayette - USA

We anticipate the application window for this opening will close on - 8 May 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 co...

8 days ago
Full Time

Executive Director, Regulatory Affairs

Msd

profile Rahway - USA

Job DescriptionThe Executive Director Chemistry Manufacturing Control for Biologics (Biologics-CMC) is accountable for managing a team of CMC professionals and ensuring rigor in CMC regulatory strategy as well as delivery of high quality CMC submissions for late phase new modality biologics products...

8 days ago
Full Time

Coordinator Of Grants & Regulatory Affairs

Lewis-clark State College

profile Lewiston - USA

LC State invites applications for the position of Coordinator of Grants & Regulatory Affairs. This position is located in Lewiston Idaho. Remote work is not available.Salary and rank based on experience and qualifications: $49754 - $57000Degree Required: Bachelors degree in a relevant discipline fro...

8 days ago
Grant