Batch Record Reviewer

Piper Companies is seeking Batch Record Reviewers to support a leading biopharmaceutical manufacturing organization. This opportunity is a 6-month contract focused on reviewing GMP batch records, supporting manufacturing and quality operations, and helping reduce a significant documentation backlog. We are seeking multiple hires and are looking to move quickly for qualified candidates with pharmaceutical manufacturing experience.

• Review batch production records for accuracy, completeness, and compliance with GMP requirements.
• Partner closely with Manufacturing, Quality Assurance, supervisors, and quality leaders to resolve documentation discrepancies and support record approval.
• Review deviations, exceptions, and supporting quality documentation to ensure compliance with site procedures and regulatory standards.
• Utilize quality and manufacturing systems to support batch record review activities and documentation workflows.
• Assist with backlog reduction efforts while maintaining attention to detail and quality standards.
• Collaborate cross-functionally with Manufacturing and QA teams within both commercial and clinical manufacturing environments.

• Minimum of 1 year of batch record review experience in a pharmaceutical manufacturing environment required.
• 3-5+ years of batch record review experience strongly preferred.
• Experience supporting biologics manufacturing is highly preferred.
• Familiarity with Quality Management Systems (QMS) and electronic quality systems.
• Experience using ERP and manufacturing systems such as SAP
  , Blue Mountain
  , or similar platforms.
• Experience reviewing deviations, exceptions, investigations, or GMP documentation preferred.
• Bachelor's degree preferred but not required.
• Strong attention to detail and ability to navigate multiple quality and manufacturing systems.

• $30-$37/hr
• Overtime opportunities expected, particularly at the beginning of the engagement.
• Contract Length: 6 Months.
• Comprehensive Benefits:
  Medical, Dental, Vision, sick leave if required by law

• Schedule:
  
  Monday-Friday, minimum 40 hours per week.
• Flexible working hours.
• Opportunity to work closely with a large Manufacturing organization (175+ employees) and Quality team (50+ employees).
• Fast, streamlined interview process consisting of a 30-minute interview with Manufacturing and Quality leadership.
• Target
  
  Start Date:
  
  ASAP.

• Posting Date: 10/20/2026
• Apply-By/Closing Date:
  Open Until Filled

Keywords: Batch Record Reviewer, Batch Record Review, GMP, Pharmaceutical Manufacturing, Biologics, Quality Assurance, QA, Manufacturing Review, Quality Review, QMS, Quality Management System, SAP, Blue Mountain, ERP, Deviations, Exceptions, GMP Documentation, Batch Release, Biopharmaceutical Manufacturing, Commercial Manufacturing, Clinical Manufacturing, Quality Systems, Regulatory Compliance.