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Piper Companies is seeking a Quality Assurance Technical Writer in Ridgefield, New Jersey to support our pharmaceutical manufacturing operations. The role focuses on authoring and revising QA documentation and ensuring alignment with FDA and GMP requirements.
The ideal candidate has 1–5 years of experience in pharmaceutical manufacturing, strong proficiency with QA documentation and Microsoft Office, and a BS in business or science.
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.
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