Quality Assurance Technical Writer

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