Pharma QA Technical Writer — On-Site, NJ

Piper Companies; Ridgefield (NJ); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Comprehensive benefits package

Job summary

Piper Companies in Ridgefield, New Jersey is seeking an experienced Quality Assurance Technical Writer to support QA documentation and Master Batch records for a growing pharmaceutical manufacturer.

The role requires working knowledge of FDA and GMP guidelines, and collaboration with manufacturing personnel to ensure accurate, compliant documentation. On-site in NJ, with a focus on sterile injectable processes and robust regulatory standards.

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.

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

Pharmaceutical manufacturing

Sterile injectable experience

Education

Bachelor's degree in science or business

Tools

Microsoft Office

Job description

Piper Companies in Ridgefield, New Jersey is seeking an experienced Quality Assurance Technical Writer to support QA documentation and Master Batch records for a growing pharmaceutical manufacturer.

The role requires working knowledge of FDA and GMP guidelines, and collaboration with manufacturing personnel to ensure accurate, compliant documentation. On-site in NJ, with a focus on sterile injectable processes and robust regulatory standards.