Drug Regulatory Affairs Jobs in Short Hills, NJ

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 - 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 - 15 days ago

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

from: resume-library.com - 10 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 - 16 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 (+1 source) - 29 days ago

Experis - Rahway, New Jersey

regular updates to management and escalates issues. MAJOR ACTIVITIES AND RESPONSIBILITIES: With the support and guidance of the Executive Director of US Regulatory Affairs, the Specialist has the following

from: resume-library.com - 3 days ago

Englewood Lab, Inc - Totowa, New Jersey

Responsibilities: Assist the Manager of Regulatory Affairs during cGMP, Environmental, and Regulatory audits. With the assistance of Head of R&D (or designee), create and collate product master files

from: resume-library.com (+1 source) - 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 - 13 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 - 23 days ago

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 - 17 days ago