Pharmaceutical Regulatory Affairs Jobs in Rahway, NJ

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Regulatory & Medical Affairs - Regulatory Studio - CMC Senior Manager  

Varite, Inc - Short Hills, New Jersey (+1 location)

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

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

Manager Global Regulatory Affairs  

Ajulia Executive Search - Princeton, NJ, United States

Manager Global Regulatory Affairs Princeton, New Jersey EU GMP requirements Must have Global Regulatory Affairs experience in the pharmaceutical or biotechnology industry. Are you looking to make

from: linkedin.com - 23 days ago

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 Manager- Technical Product Manager Regulatory Strategy  

Johnson and Johnson - Raritan, NJ

experience: * Deep knowledge of the pharmaceutical development business and prior experience in information technology supporting pharmaceutical development preferably in the global regulatory affairs domain

from: Johnson and Johnson - 2 days ago

Associate Director, Medical Scientist, US Medical Oncology, GU  

Bristol Myers Squibb - Princeton, United States

degree (MD, PhD, PharmD, DNP) Minimum 5 years of experience in pharmaceutical industry; prior experience in oncology medical affairs is preferred Demonstrates thorough understanding of medical review

from: jobrxiv.org - 11 days ago

LABORATORY TECHNICIAN  

Aurobindo Pharma USA, Inc. - Dayton, New Jersey

portfolio very quickly. The Aurolife family consists of an experienced management team with expertise in manufacturing, R&D, Quality Assurance and Quality control and regulatory affairs. In addition

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from: resume-library.com - 4 days ago

Senior Director of Translational Medicine and Clinical Pharmacology  

Sun Pharma (Taro Pharma) - Princeton, New Jersey

and external opportunities Interface broadly with key functions including discovery sciences, preclinical development groups, toxicology, clinical operations, drug metabolism, regulatory affairs, and late-stage

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from: resume-library.com - 3 days ago

IT Senior Manager, Technical Product Manager (TPM), Regulatory Excellence  

Johnson and Johnson - Raritan, NJ

of a Bachelor's degree or equivalent * At least 6 years of related experience in pharmaceutical development IT is required, preferably focused on Regulatory Affairs IT. * Practical knowledge of pharmaceutical

from: Johnson and Johnson - 7 days ago

Head of US Medical - Endocrine Medical Affairs - Job ID: 1323  

Ascendis Pharma - Princeton, New Jersey

with Compliance, Legal and Regulatory to ensure that all US Medical Affairs activities and services are fully compliant with Ascendis SOPs and US as well as global regulatory and compliance rules/law. Requirements

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from: resume-library.com (+1 source) - 5 days ago


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