Pharmaceutical Validation Jobs in New York, NY

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 - 8 days ago

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 - 15 days ago

Nesco Resource, LLC - Rush, New York

with an understanding in the sterilization process, validation support, laboratory testing in highly regulated pharmaceutical or medical device manufacturing laboratory environments, required. Strong attention to detail

from: resume-library.com (+1 source) - 13 days ago

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 - 22 days ago

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

Cresilon, Inc. - Brooklyn, New York

in chemistry, biochemistry, or related life-science discipline (Masters or Doctorate in Analytical Chemistry preferred) Preferred Qualifications: • 7+ years in medical device / pharmaceutical analytical

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

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) - 7 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 - 12 days ago