Regulatory Affairs Jobs in USA
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Senior Medical Writer
Johnson & Johnson
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...
Rems Audit Oversight Lead
Gsk
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...
Manager, Quality Assurance Operations
Catalent
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...
Medical Director, Dermatology – Us Medical Affairs
Johnson & Johnson
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...
Associate Medical Director, Us Medical Affairs, De...
Johnson & Johnson
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...
Senior Director, Global Distribution Quality
Ultragenyx Pharmaceutical
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...
Manager, Standards Management (dastfl)
Johnson & Johnson
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...
Director, Clinical Sciences, Oncology
Johnson & Johnson
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...
Director, Vitreoretinal Instrumentation Upstream
Alcon Research
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...
U.s. Project Licensing Manager
Ge Vernova
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...
Spec 3, Quality Assurance
Millenniumsoft Inc
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...
Data Entry Specialist (part-time)
Inx International Ink Co.
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...
Manager, Regulatory Strategic Planning
Abbvie
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...
Code Development Architect
City Of New York
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...
Regulatory Affairs Analyst
Johnson & Johnson
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...
Regulatory Affairs Program Manager
Philips
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...
Sr Regulatory Affairs Manager
Medtronic
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...
Sr Regulatory Affairs Manager
Medtronic
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...
Executive Director, Regulatory Affairs
Msd
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...
Coordinator Of Grants & Regulatory Affairs
Lewis-clark State College
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...