More jobs:
On-Site QA Documentation Specialist - Pharma (GMP/FDA)
Job in
Ridgefield, Bergen County, New Jersey, 07657, USA
Listed on 2026-08-07
Listing for:
Piper Companies
Full Time
position Listed on 2026-08-07
Job specializations:
-
Quality Assurance - QA/QC
QA Specialist - Analyst/Manager
Job Description & How to Apply Below
Piper Companies in Ridgefield, NJ is seeking an experienced Quality Assurance Technical Writer to join a growing pharmaceutical manufacturer. The role focuses on authoring and revising QA documentation and Master Batch Records to support sterile injectable production.
Responsibilities include reviewing alterations to master batch records, advising manufacturing personnel on documentation standards, and ensuring compliance with FDA and GMP regulations using MS Office tools.
#J-18808-LjbffrTo View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
Search for further Jobs Here:
×