Pharmaceutical Validation Jobs in Franklin Lakes, NJ

Infotree Global Solutions - Nutley, NJ, United States

Pharmaceutical client is looking for a n IT Quality Validation Consultant / Computer System Validation Consultant, who will Prepare computer validation documents such as Validation Plans, User Requirements

from: linkedin.com - 5 days ago

LanceSoft, Inc. - Nutley, 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 - 5 days ago

Hired by Matrix - Nutley, New Jersey

by joining a global pharmaceutical company? If so, our client is hiring an IT Quality Validation Consultant! What You’ll Do: Prepare computer validation documents such as Validation Plans, User Requirements

from: resume-library.com (+1 source) - 6 days ago

Integrated Resources, Inc ( IRI ) - Nutley, NJ, United States

assessments. Must be familiar with 21 CFR Part 11. Consult on Projects. Prepare Project Plans. BS in a technical field and 5 years of experience in GxP environment. Requirements: 1) Extensive Pharmaceutical

from: linkedin.com - 5 days ago

Northreach - New York, NY, United States

is preferred (M.S. with significant industry experience will also be considered) Experience in overseeing outsourced analytical tasks within the pharmaceutical development or commercial sector, encompassing

from: linkedin.com - 7 days ago

LanceSoft Inc - Nutley, New Jersey

. Must be familiar with 21 CFR Part 11. Consult on Projects. Prepare Project Plans. BS in a technical field and 5 years experience in GxP environment. Requirements: 1) Extensive Pharmaceutical Experience

from: resume-library.com - 6 days ago

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 - 10 days ago

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 - 11 days ago

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

from: resume-library.com - 11 days ago

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 - 18 days ago