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Piper Companies in Ridgefield, New Jersey is seeking an experienced Quality Assurance Technical Writer to support QA documentation and Master Batch records for a growing pharmaceutical manufacturer.
The role requires working knowledge of FDA and GMP guidelines, and collaboration with manufacturing personnel to ensure accurate, compliant documentation. On-site in NJ, with a focus on sterile injectable processes and robust regulatory standards.
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