Latest Regulatory Affairs Pharmaceutical jobs in Raritan, NJ

33 Regulatory Affairs Pharmaceutical Jobs in Raritan, NJ

Director, Regulatory Affairs Johnson and Johnson - Raritan, NJ : Employer will accept a Bachelor's degree in Regulatory Affairs, Pharmaceutical Sciences, or related field and 10 years of progressive, post-baccalaureate experience in the job offered or in a Director 3 days ago
Senior Director, Global Regulatory Leader, CAR-T Therapy Johnson & Johnson - Raritan, NJ any of the following areas (e.g. Global Regulatory Affairs, R&D or health authority role) is required. 10 years within the pharmaceutical/biotech industry is required, along with a minimum 5 years of recent regulatory USD 187,000.00 - 322,000.00 per year 15 days ago
Regulatory Affairs Specialist Project Lead I Aequor - Bridgewater, NJ, United States experience in R&D, including at least 5 years of relevant Regulatory Affairs experience (regionally and/or global). 6 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 9 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 4 days ago
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 11 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 16 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 4 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 18 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 4 days ago

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