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Regulatory Affairs Jobs in New Jersey

1 - 15 of 68
1 - 15 of 68
Search Results - Regulatory Affairs Jobs in New Jersey
Sanofi-Bridgewater (NJ)
About the RoleThe Associate Director, US Regulatory Affairs (RA) serves as the regulatory lead on relative Review Committees (RCs), for products in the Rare Disease, Rare Blood Disorder and Neurology portfolio. As the RC RA representative, work...
1 similar job: Cambridge
The Fountain Group LLC-Bridgewater (NJ)
The Fountain Group are a national staffing firm and are currently seeking a Regulatory Affairs Lead for a prominent Pharmaceutical client of ours. This position is in Bridgewater, NJ (Hybrid Role). Details for the position are as follows: Job...
resume-library.com -
NS Pharma, Inc.-Paramus
goals are developed, timelines are managed, and issues are appropriately raised and resolved in a timely manner. The Director will represent regulatory affairs on assigned project teams and support R&D and clinical research activities. Must be able...
mindmatch.ai -
Aequor Technologies LLC-Bridgewater (NJ)
US Regulatory Affairs Lead Personal Care Category  •  ------------------------------------------------------------------------------------------------ SCOPE OF RESPONSIBILITIES: " He/She will be accountable to support regulatory for Personal Care...
resume-library.com -
Spectraforce Technologies Inc-Bridgewater (NJ)
for the authoring by reaching out to appropriate internal/external functions such as quality, manufacturing, Global Regulatory Affairs (GRA), technical experts from global locations or contract manufacturing organizations (CMOs), or alliance partners. He/She...
mindmatch.ai -
Mindlance-Bridgewater (NJ)
US Regulatory Affairs Lead – Personal Care Category  •  ------------------------------------------------------------------------------------------------ SCOPE OF RESPONSIBILITIES:  •  He/She will be accountable to support regulatory for Personal Care...
resume-library.com -
Gan & Lee Pharmaceuticals-Bridgewater (NJ)
Summary This position reports to the Functional Area Head, Global Regulatory Affairs. The incumbent responsible for supporting the development and implementation of regulatory strategies, work closely with the cross functional asset teams...
mindmatch.ai -
Jersey City
Overview: Undergraduate or Graduate student in a Science discipline. This individual will work in our Regulatory Affairs Department, supporting the Regulatory Strategy group. He/she will be assigned interesting and challenging projects related...
icims.com -
Daiichi Sankyo, Inc.-New Jersey
centered around rare diseases and immune disorders. The Manager, Regulatory AffairsRegulatory Project Management (RPM) provides planning and coordination supports for global and US regulatory activities. The Manager RPM is responsible for supporting...
Katalyst Healthcares & Life Sciences-Edison (NJ)
Responsibilities: This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S. and Europe, support of international product registrations and related regulatory affairs activities...
resume-library.com -
Daiichi Sankyo, Inc.-New Jersey
centered around rare diseases and immune disorders. Job Summary: We are currently seeking a Regulatory Affairs Strategy Intern. This full time time position works for approximately 37.5 hours per week for the summer. The candidate will work closely...
Ascendis Pharma-Princeton (NJ)
The Regulatory Affairs (RA) Associate Director, Labeling will be responsible for labeling activities across programs and stages of development, with specific responsibility for the United States and the Americas and supporting global needs...
resume-library.com -
Florham Park
Overview: The Associate Director/Director, Regulatory Affairs - GDP, provides essential support to the Senior Director in overseeing regulatory activities related to Quality of Life (QOL) initiatives on a regional and/or global scale. This role...
icims.com -
Daiichi Sankyo, Inc.-New Jersey
Ph.D., MD, JD) preferred. Experience Qualifications: ~10 or More Years in the pharmaceutical industry required. ~8 or More Years in regulatory affairs ~ Experience in providing regulatory strategic input into the drug development process...
CSL Behring-Summit (NJ)
to the Head, GRA Region North America The Role The Global Regulatory Affairs (GRA) Region North America Therapeutic Area Lead (Vaccines) is a member of the GRA Regional Leadership Team and contributes to the vision and goals for Global Regulatory Affairs...
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