Pharmaceutical Regulatory Affairs Jobs in Summit, NJ

Artech LLC - Summit, New Jersey

Management, Client Affiliates, Medical Affairs (MA), Regulatory, CMC, QA, Packaging Vendors, CRO s, IRT Organizations, and Global Clinical Supply Chain Functional Operations to ensure all needs are met

from: resume-library.com - 9 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 - 14 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 - 15 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

from: resume-library.com - Yesterday

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 - 25 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

from: resume-library.com - 4 days ago

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 - 19 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 - 17 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 - 2 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

from: resume-library.com - 3 days ago