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,