Quality Assurance Technical Writer

Piper Companies is currently looking for an experienced Quality Assurance Technical Writer in Ridgefield, New Jersey (NJ) to work for an 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 #J-18808-Ljbffr Piper Companies