Pharmaceutical Regulatory Affairs Jobs in Summit, NJ

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Quality - Trial Supplies Manager Trial Supplies Manager  

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

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from: resume-library.com - 9 days ago

Senior Regulatory Affairs Associate  

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

Associate Director, US Regulatory Affairs, Advertising & Promotion  

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

Regulatory & Medical Affairs - Regulatory Studio - CMC Senior Manager  

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

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from: resume-library.com - Yesterday

Senior VP/Head of Regulatory Affairs  

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

HEOR Project Manager----Remote  

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

CMC 2 Regulatory affairs  

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

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from: resume-library.com - 4 days ago

Manager/Sr. Manager Regulatory Affairs Strategy  

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

Regulatory Operations Specialists - II (Associate)  

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

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from: resume-library.com - 2 days ago

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CMC Manager  

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

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from: resume-library.com - 3 days ago


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