Pharmaceutical Validation Jobs in Berkeley Heights, NJ

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Validation Specialist - (MES) Manufacturing Execution System  

TSR Consulting Services, Inc. - Summit, NJ, United States

TSR is a premier National U.S. Staffing company with over 50 years of staffing excellence. Our client, a leading Pharmaceutical company is hiring a MES Validation Specialist. Rate type: W2 only

from: linkedin.com - 18 days ago

Netsuite Architect  

PRI Technology - Jersey City, NJ, United States

three (3) years of relevant experience in the pharmaceuticals, medical device, or life science industry. Working knowledge of GLP, GDP and GMP, including Computer Systems Validation Prior hands

from: linkedin.com - 8 days ago

Quality Assurance Equipment/Computer System Validation Specialist II  

Johnson and Johnson - Raritan, NJ

Janssen Pharmaceutical, a member of Johnson & Johnson's Family of Companies, is recruiting for a Quality Assurance Equipment/Computer System Validation Specialist II-CAR-T Manufacturing

from: Johnson and Johnson - 2 days ago

Packaging Engineer  

LanceSoft, Inc. - Franklin Lakes, NJ, United States

field and 5 years of experience in GxP environment. Requirements: Extensive Pharmaceutical Experience with 10 years plus in writing IT system validation protocols including IQs/OQs/PQs, project summary

from: linkedin.com - 12 days ago

Quality Assurance Batch Reviewer  

the ASSURANCE group - Wharton, NJ, United States

relevant experience in validation / batch processing role (regulated Cosmetic or Pharmaceutical industry) Familiar with validation discipline and processes. Familiar with CAPAs, Change Controls, OTC, FDA

from: linkedin.com - 17 days ago

Sr. Validation Engineer  

Katalyst Healthcares & Life Sciences - Summit, New Jersey

in validation, biological quality assurance and/or quality control in an FDA-regulated biotechnology or pharmaceutical company with progressive levels of responsibility. 1-3 years in a quality assurance

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from: resume-library.com - 18 days ago

Director/Senior Director, Quality Control  

Lexeo Therapeutics - New York, NY, United States

drug submissions IND, BLA, etc. Experience with pharmaceutical drug-process validation and manufacture Strong knowledge of FDA, cGMPs, and ICH guidelines and QBD principles pertaining to analytical

from: linkedin.com - 21 days ago

Technical Writer  

Trinity Consultants - Advent Engineering Life Science Solutions - , NY, United States

and commissioning, validation and compliance consulting for distinguished and successful biotechnology and pharmaceutical manufacturing companies. The successful candidate will work with a group of engineers involved

from: linkedin.com - 28 days ago

Contract Analytical Research and Development Chemist  

Lupin Pharmaceuticals Inc. - Somerset, New Jersey

, etc. Experience in pharmaceutical Method Development, Method Validation and stability testing. Capable of writing reports suitable for regulatory submission with minimum supervision. Physical

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from: resume-library.com - 12 days ago

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Manager, Validation Lead  

Daiichi Sankyo, Inc. - Bernards, NJ

-hand knowledge of GAMP5, GxP and Non-GxP computer system validation and qualification and Computer Software Assurance (CSA), SDLC related to pharmaceutical operations. required - 1 or More Years Direct

from: Pharmadiversityjobboard.com (+1 source) - 15 days ago


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