Pharma QA Technical Writer — Master Batch Records & GMP

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 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.