Quality Assurance Technical Writer - 171852

ZP Group; Ridgefield (NJ); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Comprehensive benefits package

Job summary

Piper Companies is seeking an experienced Quality Assurance Technical Writer for our Ridgefield, NJ location. The role involves authoring and revising QA documentation including Master Batch Records and related documents to ensure compliance with FDA/GMP regulations.

Ideal candidates will have 1–5 years in pharmaceutical manufacturing, hands-on QA documentation experience, and proficiency in Microsoft Office. A BS in business or a scientific field is preferred.

Qualifications

• 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.

Responsibilities

• 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

Skills

QA documentation

Experience 1-5 years

Hands-on QA documentation

Microsoft Office proficiency

Education

B.S. in business or scientific field

Tools

Microsoft Office

Job description

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

• 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

• 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

• 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