Pharma QA Technical Writer — Master Batch & Compliance

Zachary Piper Solutions; 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 a Quality Assurance Technical Writer in Ridgefield, New Jersey to support our pharmaceutical manufacturing operations. The role focuses on authoring and revising QA documentation and ensuring alignment with FDA and GMP requirements.

The ideal candidate has 1–5 years of experience in pharmaceutical manufacturing, strong proficiency with QA documentation and Microsoft Office, and a BS in business or science.

Qualifications

• 1–5 years of experience in pharmaceutical manufacturing (sterile injectable preferred).
• Hands-on experience with QA documentation.
• Proficiency in Microsoft Office.
• BS in business or scientific field preferred.

Responsibilities

• Review and author/maintain alterations to Master Batch records and QA documentation.
• Correct and revise documentation as needed.
• Advise manufacturing personnel on proper documentation.
• Apply FDA and GMP knowledge to ensure compliance.

Skills

QA documentation

Microsoft Office

Pharmaceutical manufacturing

Education

Bachelor's degree in business or science

Job description

Piper Companies is seeking a Quality Assurance Technical Writer in Ridgefield, New Jersey to support our pharmaceutical manufacturing operations. The role focuses on authoring and revising QA documentation and ensuring alignment with FDA and GMP requirements.

The ideal candidate has 1–5 years of experience in pharmaceutical manufacturing, strong proficiency with QA documentation and Microsoft Office, and a BS in business or science.