Pharma QA Specialist: Batch Records & GMP Compliance

Piper Companies; 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 seeking an experienced Quality Assurance Specialist in Audubon, PA to ensure batch records are complete and accurate for release. You will review, correct, and advise on documentation while applying FDA and GMP knowledge to maintain compliance.

Ideal candidates have 1–5 years in pharmaceutical manufacturing, hands-on batch record review, and proficiency with Microsoft Office. A science or business degree is preferred, with a solid foundation in quality documentation.

Qualifications

• 1–5 years’ experience within Pharmaceutical Manufacturing.
• Hands on experience with Batch Record review.
• Proficiency in Microsoft Office.
• B.S. in business or scientific field preferred.

Responsibilities

• Review batch records and documentation for completeness and accuracy 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

Documentation

Education

B.S. in business or scientific field

Job description

Piper Companies is seeking an experienced Quality Assurance Specialist in Audubon, PA to ensure batch records are complete and accurate for release. You will review, correct, and advise on documentation while applying FDA and GMP knowledge to maintain compliance.

Ideal candidates have 1–5 years in pharmaceutical manufacturing, hands-on batch record review, and proficiency with Microsoft Office. A science or business degree is preferred, with a solid foundation in quality documentation.