Drug Regulatory Affairs Jobs in Bayonne, NJ

Food and Drug Administration - Bayonne, 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 - 12 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 - 22 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 - 8 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 - 16 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 - 9 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 - 29 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

from: resume-library.com - 3 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 - 6 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 - 19 days ago

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 - 5 days ago