Drug Regulatory Affairs Jobs in Newark, NJ
Food and Drug Administration - Newark, New Jersey (+9 locations)
Services (DHHS), Food and Drug Administration (FDA), Office of Regulatory Affairs (ORA), Office of Medical Products and Tobacco Operations (OMPTO), Office of Biological Products Operations (OBPO), which
from: Usajobs.gov - 11 days ago
Breckenridge Pharmaceutical, Inc. - Berkeley Heights, NJ, United States
regulatory affairs operations. Knowledge of eCTD publishing systems and standards, EDMS technology and related publishing tools. Working knowledge of US FDA (OGD/CDER) e-submission requirements. Strong written
from: linkedin.com - 7 days ago
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 - 21 days ago
Shionogi Inc. - Florham Park, New Jersey
throughout the project lifecycle. Collaborate with cross-functional teams including research, clinical development, medical and regulatory affairs, and commercial teams to drive successful drug development
Register your RESUMEfrom: resume-library.com - 2 days ago
Proclinical Staffing - Morristown, NJ, United States
Regulatory Affairs representative, you will work with brand on competitively positioning assigned products appropriately while maintaining compliance with applicable FDA regulations, company policies
from: linkedin.com - 8 days ago
Breckenridge Pharmaceutical, Inc. - Berkeley Heights, NJ, United States
and through strategic partnerships with manufactures from around the world. JOB SUMMARY: The Senior Associate, Regulatory Affairs is responsible for supporting applications under pre and post approval
from: linkedin.com - 28 days ago
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 - 15 days ago
Merck - Rahway, NJ 07065
Team. Strong organizational, time management, and multi-project coordination skills Broad knowledge of Clinical Development and Regulatory Affairs requirements Ability to multi-task, work independently
from: Pharmadiversityjobboard.com - 5 days ago
Johnson and Johnson - Raritan, NJ
for clinical 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
from: Johnson and Johnson - 8 days ago
Merck - Rahway, NJ 07065
with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects. Assist the Executive Director in ensuring
from: Pharmadiversityjobboard.com - 18 days ago
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