Pharmaceutical Regulatory Affairs Jobs in Dayton, NJ

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Safety Case Management Product Specialist  

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 - 7 days ago

GPV Submission Specialist  

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 - 9 days ago

Pharma Business Analyst with Regulatory Experience  

Cynet Systems - Princeton, NJ

Job Type: Contract Job Description: Pay Range: $60hr - $65hr Requirements: 7+ years of experience as BA. Working knowledge of Pharmaceutical R&D Life Sciences. Specific knowledge of Global Regulatory Affairs Depends on Experience

from: Dice.com - 3 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) - 11 days ago

Consultant Regulatory Affairs Associate  

Lupin Pharmaceuticals Inc. - Somerset, New Jersey

in the pharmaceutical industry with 1-2 of those years in regulatory affairs preferred Lupin is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment

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from: resume-library.com - 13 days ago

usa-regulatory affairs specialist project lead i (scientific- first shift  

Randstad - bridgewater, new jersey (remote)

of relevant pharmaceutical/biotechnology experience in R&D, including at least 5 years of relevant Regulatory Affairs experience (regionally and/or global), in early development. Must have: - Leadership $89 - $91.11 per hour

from: randstadusa.com - 3 days ago

USA-Regulatory Affairs Specialist Project Lead I (Scientific)  

Mindlance - Bridgewater, New Jersey

years of relevant pharmaceutical/biotechnology experience in R&D, including at least 5 years of relevant Regulatory Affairs experience (regionally and/or global). EEO: “Mindlance is an Equal Opportunity

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from: resume-library.com - 2 days ago

USA-Regulatory Affairs Specialist Project Lead I (Scientific)  

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

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from: resume-library.com - 2 days ago

Manager Global CMC Regulatory Affairs  

Johnson and Johnson - Raritan, NJ

Affairs * Conducts due diligence/licensing evaluations where needed * Bachelors in Science (engineering, biological, pharmaceutical or chemical) with minimal 6 years of proven experience or equivalent

from: Johnson and Johnson - 7 days ago

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CMC2 - Regulatory Affairs - Animal Health  

Diverse Lynx - Rahway, New Jersey

. Qualifications we seek in you! Experience should be 4 to 7 years Bachelor's or master s degree required in science, engineering or related field (advanced degree preferred). Proven and relevant regulatory affairs

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from: resume-library.com - 5 days ago


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