Pharmaceutical Regulatory Affairs Jobs in Raritan, NJ
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 - 3 days ago
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 - 8 days ago
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GForce Life Sciences - Princeton, NJ, United States
experience processing AE/SAE reports, generating narratives, queries, working within safety databases, and experience with regulatory submissions **Relevant experience includes experience in the pharmaceutical
from: linkedin.com - 6 days ago
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GForce Life Sciences - Princeton, NJ, United States
experience processing AE/SAE reports, generating narratives, queries, working within safety databases, and experience with regulatory submissions **Relevant experience includes experience in the pharmaceutical
from: linkedin.com - 8 days ago
![](https://logos-cdn.jobisjob.com/sites/2358-2.png)
The Fountain Group LLC - Bridgewater, New Jersey
and strategy in collaboration with GRT (Global Regulatory Team) and is accountable for the communication of the key outcomes to senior management. Experience: • At least 8-10 years of relevant pharmaceutical
Register your RESUMEfrom: resume-library.com - 19 days ago
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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
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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
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Mindlance - Bridgewater, New Jersey
years of relevant Regulatory Affairs experience (regionally and/or global), in early development. EEO: “Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis
Register your RESUMEfrom: resume-library.com - 19 days ago
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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 - 24 days ago
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CMK Select - Trenton, NJ, United States
CMK Select, a specialized project management consulting firm dedicated exclusively to the Pharmaceutical / Life Sciences industry is hiring a skilled Medical Affairs Program Manager to oversee
from: linkedin.com - 15 days ago
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