Pharma QA Technical Writer — On-Site, NJ

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

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