Pharmaceutical Validation Jobs

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 - 6 days ago

Randstad Life Sciences US - Melrose Park, IL, United States

documents and product testing reports. REQUIREMENTS High school graduate with some college preferred. 3-5 years’ experience in the pharmaceutical industry. Knowledge of computerized record tracking systems

from: linkedin.com - 5 days ago

Randstad Sourceright - Smyrna, GA, United States

experience in Omnichannel/marketing automation systems.(Specifically SalesForce Marketing Cloud) 4+ years of experience in the Pharmaceutical industry Experience in the support of computerized System

from: linkedin.com - 6 days ago

Redbock - an NES Fircroft company - Los Angeles, CA, United States

of experience as a Validation Engineer working with Medical Device and Pharmaceutical companies 5+ years of direct lab experience validating lab equipment, this experience must be clearly detailed in CV Strong

from: linkedin.com - 6 days ago

PharmaLex - , NC, United States

combination of education and experience 10+ years of direct expertise working within the pharmaceutical, biotech, or medical device industry In-depth understanding of regulatory standards in pharmaceutical

from: linkedin.com - 6 days ago

SciPro - Raleigh, NC, United States

environment in the Pharmaceutical or Biotech space Experienced in Validation / Qualification of products and processes in a Drug Product and Drug Substance environment Hands-on experience in Tech Transfer

from: linkedin.com - 29 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 - 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 - 6 days ago

Intelliswift Software - ST Louis, MO, United States

qualification and validation of test methods for pharmaceutical concentration, purity, and impurity testing. • Assists in preparing regulatory documents and other communications with outside agencies, clients

from: linkedin.com - 6 days ago

Planet Pharma - Horsham, PA, United States

installations and validations within cGMP and non-cGMP facilities.? In this role the validation technician travels (at least 80% of the time) to various life science (pharmaceutical manufacturers, research labs

from: linkedin.com - 9 days ago