Drug Regulatory Affairs Jobs in Rahway, NJ

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Associate Director-Quality Assurance (QA-CMC)  

Clinical Dynamix - Jersey City, NJ, United States

research labs (CROs). This individual will partner with CMC, Clinical, Regulatory Affairs, and other corporate stakeholders to ensure Company’s clinical and commercial products follow cGMP framework

from: linkedin.com (+1 source) - 30 days ago

Senior Director, Drug Development, Project Management - Rare Diseases (Pompe Disease)  

Shionogi Inc. - Florham Park, New Jersey

, medical and regulatory affairs, and commercial teams to drive successful drug development programs. Provide strategic guidance and decision support to senior management on project priorities, resource

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from: resume-library.com - 11 days ago

Global Regulatory Lead, Oncology, Global Regulatory Strategy & Policy (Associate Director) - Princeton, NJ (Hybrid)  

HUMAC INC. - Princeton, NJ

experience in regulatory affairs (e.g., 3-5 years) Key Competency Required: Expert understanding of policy, laws, regulations, and guidelines as they apply to U.S. FDA for drug development and approval. Expert Depends on Experience

from: Dice.com - 7 days ago

Vice President, Oncology Breast Therapeutic Area Medical Head , NMD at Pfizer  

Pfizer - New York City, New York

potential of our existing and future commercially available medicines. + The role will partner closely with Pfizer Oncology stakeholder groups (including Research, Early and Late Development, Regulatory

from: HealtheCareers.com - 24 days ago

Associate Director, Clinical Sciences - Ophthalmology  

Johnson & Johnson - Raritan, NJ

data review, including medical data review, coding, in conjunction with other clinical team members. OTHER RESPONSIBILITIES / DETAILED DUTIES: Assists Regulatory Affairs in the development of drug USD 135,000.00 - 232,300.00 per year

from: Dice.com - 18 days ago

Global Regulatory Lead  

Cloudious LLC - Princeton, NJ

experience in regulatory affairs (e.g., 3-5 years) Key Competency Required: Expert understanding of policy, laws, regulations, and guidelines as they apply to U.S. FDA for drug development and approval. Expert

from: Dice.com - 20 days ago

Director, Global Regulatory Affairs (GRL)  

Daiichi Sankyo, Inc. - Bernards, NJ

Years of proven experience in a regional regulatory lead role 7 or More Years of relevant pharmaceutical experience including 5 years of experience within Regulatory Affairs Knowledge of IND, NDA/BLA

from: careerbuilder.com - 6 days ago

Director, Regulatory Affairs  

Daiichi Sankyo, Inc. - Bernards, NJ

. Experience Qualifications: 10 or More Years in the pharmaceutical industry required. 7 or More Years in regulatory affairs Experience in providing regulatory strategic input into the drug development process

from: careerbuilder.com - 13 days ago

Director, US Regulatory Affairs Strategy  

Daiichi Sankyo, Inc. - Bernards, NJ

. 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

from: careerbuilder.com - 14 days ago


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