Pharma QA Specialist - Batch Release & Compliance

Piper Companies; Ridgefield (NJ); On-site; USD 65,000 - 95,000; Full time

Benefits offered by this job

Comprehensive benefits package

Job summary

Piper Companies is seeking an experienced Quality Assurance Specialist in Ridgefield, New Jersey to support a growing pharmaceutical manufacturer. The role focuses on reviewing electronic batch records, ensuring completeness and accuracy, and advising manufacturing teams on proper documentation.

Candidate requirements include 1–5 years in pharmaceutical manufacturing (sterile injectable preferred) and experience with batch record review.

Qualifications

• 1-5 years’ experience in Pharmaceutical Manufacturing (sterile injectable preferred).
• Hands-on batch record review experience.
• Proficiency with Microsoft Office.
• B.S. in business or scientific field preferred.

Responsibilities

• Review commercial electronic batch records and documentation for completeness and accuracy prior to batch release.
• Correct and revise documentation as needed.
• Advise manufacturing personnel on proper documentation.
• Apply knowledge of FDA and GMP regulations to ensure compliance.
• Conduct investigations for Deviation/OOS.

Skills

Batch record review

Documentation review

Attention to detail

Education

B.S. in business or scientific field

Tools

Microsoft Office

Job description

Piper Companies is seeking an experienced Quality Assurance Specialist in Ridgefield, New Jersey to support a growing pharmaceutical manufacturer. The role focuses on reviewing electronic batch records, ensuring completeness and accuracy, and advising manufacturing teams on proper documentation.

Candidate requirements include 1–5 years in pharmaceutical manufacturing (sterile injectable preferred) and experience with batch record review.