Pharmaceutical Product Development Jobs in Jersey City, 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

Director CMC  

Clinical Dynamix, Inc. - Jersey City, NJ, US

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

from: jobvertise.com - 30 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 - 21 days ago

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 - 27 days ago

Sr. Manager Solution Engineer / Specialty Product Owner  

Pfizer - New York City, NY

Proven experience on driving product roadmaps and releases navigating via inter-dependencies across multiple internal and external teams. Nice to Have: Extensive bio-pharmaceutical industry experience USD 117,300.00 - 195,500.00 per year

from: Dice.com - 19 days ago

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 - 12 days ago

Stability Scientist  

LanceSoft, Inc. - New Brunswick, NJ, United States

Substance and Drug Product manufacturing and good understanding of analytical and/or Microbiology methods. Very good skills to drive development of technical or scientific initiatives for solving complex

from: linkedin.com - 8 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 - 3 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 - 16 days ago

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Medical Publications Manager  

US Tech Solutions - Plainsboro, NJ, United States

, pharmaceutical and biotech companies, Regulatory affairs writing, medical information, product safety, medical affairs. MD PhD or Pharm D strongly preferred/required CMPP Certification optional The Manager

from: linkedin.com (+1 source) - 17 days ago


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