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 Qualifications for the Quality Assurance Technical Writer include: · 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 Compensation for the Quality Assurance Technical Writer include: · Salary Range is dependent upon experience. · Comprehensive benefits package Keywords 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