More jobs:
Quality Assurance Technical Writer
Job in
Ridgefield, Bergen County, New Jersey, 07657, USA
Listed on 2026-09-21
Listing for:
Piper Companies
Full Time
position Listed on 2026-09-21
Job specializations:
-
Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers, Regulatory Compliance Specialist -
Pharmaceutical
Regulatory Compliance Specialist
Job Description & How to Apply Below
Piper Companies is currently looking for an experienced Quality Assurance Technical Writer in Ridgefield, New Jersey (NJ) to work for a innovative and growing pharmaceutical manufacturer.
Responsibilities for the Quality Assurance Technical Writer include:- Review and act as author/technical writer to alterations to Master Batch record and QA documentation
- Correct and revise documentation as needed
- Advise manufacturing personnel on proper documentation
- Utilize knowledge of FDA and GMP regulations to ensure compliance
- A minimum of 1-5 years’ experience within Pharmaceutical Manufacturing (sterile injectable is preferred)
- Hands on experience with QA documentation
- Proficiency in Microsoft Office
- B.S. in business or scientific field preferred
- Salary Range is dependent upon experience.
- Comprehensive benefits package
Quality Assurance Technical Writer, QA, Pharmaceutical, Branchburg, NJ, New Jersey, FDA, GMP, Batch Record, Manufacturing, GDP, cGMP, Clinical Manufacturing, Regulatory Review, #LI-ONSITE #LI-DF1
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