QA Specialist: Pharma Batch Records & Compliance

Zachary Piper Solutions; Lower Providence Township (PA); On-site; USD 65,000 - 73,000; Full time

Benefits offered by this job

Comprehensive benefits package

Job summary

Piper Companies is currently looking for an experienced Quality Assurance Specialist in Audubon, Pennsylvania to work for a pharmaceutical manufacturer. Responsibilities include reviewing batch records for completeness and accuracy, advising manufacturing personnel on proper documentation, and ensuring FDA and GMP compliance.

The role also supports deviation and OOS investigations. This role requires 1–5 years of experience in pharmaceutical manufacturing, strong MS Office skills, and a BS in a

Qualifications

• 1–5 years of experience within pharmaceutical manufacturing.
• Hands-on batch record review experience.
• Proficiency in Microsoft Office.
• BS in business or scientific field preferred.

Responsibilities

• Review batch records and documentation for completeness and accuracy in preparation for batch release.
• Correct and revise documentation as needed.
• Advise manufacturing personnel on proper documentation.
• Utilize knowledge of FDA and GMP regulations to ensure compliance.
• Assist in Deviation/OOS investigations.

Skills

Batch Record review

Microsoft Office

Education

BS in business or scientific field preferred

Job description

Piper Companies is currently looking for an experienced Quality Assurance Specialist in Audubon, Pennsylvania to work for a pharmaceutical manufacturer. Responsibilities include reviewing batch records for completeness and accuracy, advising manufacturing personnel on proper documentation, and ensuring FDA and GMP compliance.

The role also supports deviation and OOS investigations. This role requires 1–5 years of experience in pharmaceutical manufacturing, strong MS Office skills, and a BS in a