Quality Assurance Technical Writer - 171852

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 Writerinclude:

·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 Writerinclude:

·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