Pharmaceutical Regulatory Affairs Jobs in Somerset, NJ

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Manager, Regulatory Affairs  

Lupin Pharmaceuticals Inc. - Somerset, New Jersey

years’ experience in the pharmaceutical industry with 3‐5 of those years in regulatory affairs preferred Prior experience of participating in managing, designing and implementing REMS systems (highly

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from: resume-library.com - 3 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 - 15 days ago

Regulatory Affairs Specialist Project Lead I (Scientific)  

Sanofi - Bridgewater, NJ, United States

/biotechnology experience in R&D , including at least 5 years of relevant Regulatory Affairs experience (regionally and/or global). Please contact me if you are interested. Thank you. Please fill below details

from: linkedin.com - 2 days ago

Regulatory Manager  

Mindlance - Bridgewater, NJ, United States

of relevant Regulatory Affairs experience (regionally and/or global), in early development.

from: linkedin.com - 2 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 - 4 days ago

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 - 9 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 - 11 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 - 4 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 - 19 days ago

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USA-Regulatory Affairs Specialist Project Lead I (Scientific)  

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

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from: resume-library.com - 2 days ago


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