Pharmaceutical Product Development Jobs in Parsippany, NJ

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Director of CMC  

Clinical Dynamix - Jersey City, NJ, United States

updated in industry trends, technological advancements, and regulatory changes related to pharmaceutical development and manufacturing. Requirements and Preferred Skills: MS and/or PhD (preferred

from: linkedin.com - 29 days ago

Senior Quality Assurance Specialist  

Germer International - Pharmaceutical Recruiting - Piscataway, NJ, United States

in real-time to maintain manufacturing efficiency and product quality. Qualifications: Bachelor's degree Experience in formulation development within the pharmaceutical industry, with a strong understanding

from: linkedin.com - 30 days ago

Marketing/Communications - 3D Digital Designer II 3D Digital Designer II  

Softpath System LLC - Short Hills, New Jersey

guidelines and relevant applications. " Ph. Eur requirements for veterinary products and guidance (not limited to QRD veterinary template, guideline on SPCs for antimicrobials, MRL etc.) " Lead development

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from: resume-library.com - 6 days ago

CMC 2 Regulatory affairs  

Ampcus Incorporated - Short Hills, New Jersey (+1 location)

and relevant applications. • Ph. Eur requirements for veterinary products and guidance (not limited to QRD veterinary template, guideline on SPCs for antimicrobials, MRL etc.) • Lead development and execution

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from: resume-library.com - 6 days ago

Senior Specialist, Clinical Supplies Project Manager  

Merck - Rahway, NJ 07065

partner organizations such as Clinical Sciences and Study Management (CSSM), Regulatory, Chemistry, Manufacturing and Controls (CMC), Pharmaceutical Sciences, Formulation Development, and Global Development

from: Pharmadiversityjobboard.com - 3 days ago

Publications Manager I  

Artech LLC - Plainsboro, New Jersey

and communication agencies, pharmaceutical and biotech companies, Regulatory affairs writing, medical information, product safety, medical affairs. MD PhD or Pharm D strongly preferred/required CMPP Certifcation

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from: resume-library.com - 3 days ago

The Associate Director, Global Labelling Strategy  

Katalyst Healthcares & Life Sciences - South Plainfield, New Jersey

of the dynamics and purpose of the Company Core Data Sheets (CCDS) and the implications of the CCDS. A understanding of pharmaceutical drug development. Previous experience with Health Authorities bodies Proven

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from: resume-library.com - 5 days ago

Senior Manager- Technical Product Manager Regulatory Strategy  

Johnson and Johnson - Raritan, NJ

. Responsibilities : The IT Senior Manager, Technical Product Manager for Regulatory Insights and Experience combines consulting, modern Information Technology (IT) expertise, and knowledge of the pharmaceutical

from: Johnson and Johnson - 4 days ago

Regulatory Operations Specialist  

Primary Talent Partners - Rahway, New Jersey

or law - OR- Master’s degree in a relevant discipline Regulatory and/or product development experience Strong written and oral communication skills Excellent people, communication and leadership skills

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from: resume-library.com - 5 days ago

Manager, Global Labeling Product Leader  

Johnson and Johnson - Raritan, NJ

within a regulatory labeling function developing labeling content for pharmaceutical products is highly preferred. * Experience working in documentum-based systems preferred * Experience leading project

from: Johnson and Johnson - 5 days ago


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