Pharmaceutical Regulatory Affairs Jobs in Jersey City, NJ
US Tech Solutions - New York, NY, United States
launches (medical affairs, commercial/marketing, market access, clinical development, regulatory, etc.). Minimum 5+ years of full-time pharmaceutical industry or consulting experience in HEOR required
from: linkedin.com - 20 days ago
Leaman Life Sciences - Newark, NJ, United States
regulatory implications for business decisions. Team Leadership: Provide leadership, mentorship, and development opportunities for the regulatory affairs team, fostering a culture of excellence, innovation
from: linkedin.com - 26 days ago
Varite, Inc - Short Hills, New Jersey
Job Description: Regulatory & Medical Affairs - Regulatory Studio - CMC Senior Manager Location: Hybrid (50% onsite) at either Lawrenceville in US or (US 100% Remote) PREREQUISITES BS/BA degree
Register your RESUMEfrom: resume-library.com - 2 days ago
The Judge Group - Paramus, NJ, United States
lead supporting clinical development project teams and global project teams in early and late-stage development (i.e., Phase 1-3). Regulatory affairs strategy experience and understanding of CMC
from: linkedin.com - 18 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
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
Register your RESUMEfrom: resume-library.com - 3 days ago
Proclinical Staffing - Morristown, NJ, United States
Associate Director, US Regulatory Affairs, Advertising & Promotion - Permanent - NJ & MA Proclinical is seeking an Associate Director, US Regulatory Affairs, Advertising & Promotion for a large
from: linkedin.com - 16 days ago
Ampcus Incorporated - Short Hills, New Jersey (+1 location)
to 7 years • Bachelor's or master’s degree required in science, engineering or related field (advanced degree preferred). • Proven and relevant regulatory affairs experience in pharmaceutical, vaccine
Register your RESUMEfrom: resume-library.com - 5 days ago
Katalyst Healthcares & Life Sciences - South Plainfield, New Jersey
and relevant regulatory affairs experience in pharmaceutical, vaccine, or biological products; or related fields Marketing authorization experience. Proven Project Management experience
Register your RESUMEfrom: resume-library.com - 4 days ago
Abbvie - Florham Park, NJ
with regulatory. activities. Qualifications Advanced Degree PhD or PharmD. Additional post doctorate experience highly preferred. Typically, 5-105 years of experience in the pharmaceutical industry or equivalent
from: Dice.com (+2 sources) - 26 days ago
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