Pharmaceutical Product Development Jobs in Paramus, NJ

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Senior Regulatory Affairs Associate  

Breckenridge Pharmaceutical, Inc. - Berkeley Heights, NJ, United States

or product development operations. Familiar with cGMP/cGCP requirements. Required to attend off-hours teleconferences with overseas partners.

from: linkedin.com - 10 days ago

Generic Pharmaceuticals - Senior Formulation and Technical Services Scientists - Solids, Semi-Solids, Steriles  

Chartwell Pharmaceuticals - Congers, NY, United States

with solids, liquids, semi-solids, ophthalmic/otic, and injectable products. Must have a current understanding of formulation development, QbD, and tech transfer process from kick-off through validation

from: linkedin.com - 19 days ago

Summer Intern - Finance  

Sun Pharma (Taro Pharma) - Hawthorne, New York

Taro is a multinational, science-based pharmaceutical company dedicated to meeting the needs of its customers through the discovery, development, manufacturing and marketing of the highest quality

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from: resume-library.com - 5 days ago

HEOR Project Manager----Remote  

US Tech Solutions - New York, NY, United States

; economic modeling studies ; familiarity with COA/PRO development, validation research and clinical trial implementation. Experience with industry cross-collaboration amongst functions involved in product

from: linkedin.com - 19 days ago

Clinical Pharma Project Manager  

Ehub Global Inc - Rahway, NJ, United States

training courses to increase project management knowledge and understanding of product development in the pharmaceutical industry and improve leadership skills. Qualifications: Education: A bachelor's degree

from: linkedin.com - 14 days ago

Director, Schizophrenia Adjunct, LAI, and Future Indications Lead  

DeBellis, Catherine & Morreale - Florham Park, New Jersey

with pharmaceutical product development, either new products or new indications Experience in creating product development plans in partnership with R&D Strong analytical and strategic marketing skills A successful

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from: resume-library.com - Yesterday

Senior VP/Head of Regulatory Affairs  

Leaman Life Sciences - Newark, NJ, United States

the pharmaceutical or biotechnology industry, with significant experience in ophthalmic product development. Demonstrated expertise in developing and executing successful global regulatory strategies for ophthalmic

from: linkedin.com - 25 days ago

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 - 27 days ago

Regulatory & Medical Affairs - Regulatory Studio - CMC Senior Manager  

Varite, Inc - Short Hills, New Jersey

will include, but are not limited to, the following: 1. Participate in the development of the CMC regulatory strategy for post-approval small molecule product submissions, including global supplements/variations

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from: resume-library.com - Yesterday

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

Softpath System LLC - Short Hills, New Jersey

" A understanding of pharmaceutical drug development. " Previous experience with Health Authorities bodies " Proven understanding of the dynamics and purpose of the Target Product Labeling and Company Core Data

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from: resume-library.com - 4 days ago


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