Batch Record Review Specialist

Piper Companies is seeking a Batch Record Review Specialist who will be responsible for reviewing executed batch records and related manufacturing documentation to ensure accuracy, completeness, and compliance with cGMP, regulatory requirements, and internal quality standards. This role is critical to supporting timely batch disposition and ensuring the release of safe, high-quality biopharmaceutical products. Responsibilities of the Batch Record Review Specialist: Review executed batch records (EBRs) for completeness, accuracy, and adherence to GDP (Good Documentation Practices) Verify manufacturing, packaging, and testing steps against approved master batch records and SOPs Identify, document, and escalation discrepancies, deviations, and non-conformances Ensure all critical process parameters, in-process controls, and documentation are properly completed Review supporting documentation, including logbooks, labels, and QC data Collaborate with Manufacturing, Quality Control, and Validation teams to resolve issues impacting batch release Support batch disposition activities, ensuring timely and compliant product release Review deviations, investigations, and CAPAs for completeness and impact on product quality Participate in internal audits, inspections, and continuous improvement initiatives Qualifications of the Batch Record Review Specialist: 2-5+ years of experience in pharmaceutical or biopharmaceutical manufacturing or quality assurance Strong knowledge of cGMP, GDP, and regulatory requirements Experience reviewing batch records, manufacturing documentation, or QA disposition preferred Prior experience working in manufacturing (upstream/allstream/support services) would be a plus Bachelor's degree in Biology, Chemistry, Pharmaceutical Sciences, or related field Compensation of the Batch Record Review Specialist: Salary: Between $65,000- $85,000 based on years of relevant experience Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO (Paid Time Off), Paid Holidays, Sick Leave as required by law This job opens for applications on 8/18/2026. Applications for this job will be accepted for at least 30 days from the posting date Keywords: Executed Batch Records, EBR, Electronic Batch Record, batch record review, batch record, master batch record, MBR, batch disposition, lot release, right first time, RFT, good documentation practices. GDP, documentation review, record reconciliation, data integrity, SIMPL, ALCOA, ALCOA+, biopharmaceutical manufacturing, aseptic processing, fill-finish operations, fill finish, central service, upstream, downstream, upstream processing, downstream processing, cleanroom operations, line clearance, in-process controls, process validation, tech transfer support, cGMP, GMP compliance, FDA regulations, EMA regulations, quality assurance, QA, quality systems, audit readiness, inspection support, regulatory compliance, SOP adherence, change control, deviations, CAPA, corrective and preventive actions, root cause analysis, non-conformance, NCR, investigation support, exception review, risk assessment, QC data review, certificate of analysis, CoA, analytical testing, environmental monitoring, EM, label reconciliation, logbook review, validation protocols, electronic batch records, EBR systems, MES, PAS-X, ERP, SAP, Oracle, LIMS, TrackWise, Veeva, MasterControl, document management systems, DMS, eDMS, cross-functional collaboration, issue escalation, workflow management, turnaround time optimization, continuous improvement, pharmaceutical, pharma, biopharma, biotech, cleanroom

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