Pharmaceutical Regulatory Affairs Jobs in Dayton, NJ

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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 - 3 days ago

CMC 2 Regulatory affairs  

Katalyst Healthcares & Life Sciences - Rahway, New Jersey

and relevant regulatory affairs experience in pharmaceutical, vaccine, or biological products; or related fields. Knowledge and hands on experience on Animal Health CMC. Marketing authorization experience

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from: resume-library.com - 4 days ago

Regulatory Operations Specialists - II (Associate)  

Experis - Rahway, New Jersey

regular updates to management and escalates issues. MAJOR ACTIVITIES AND RESPONSIBILITIES: With the support and guidance of the Executive Director of US Regulatory Affairs, the Specialist has the following

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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 - 8 days ago

Quality Assurance Analyst  

Cronus Pharma - New Brunswick,New Jersey

Overview Pharmaceutical company looking for an experienced Quality Assurance and Regulatory Affairs Associate. Ideal candidates should have experience within QA and/or Regulatory Affairs department $50000-60000 k per Yearly

from: sulekha.com - 18 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 - 27 days ago

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 - 25 days ago

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 - 19 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

from: Dice.com - 30 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 - 19 days ago


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