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Hourly Batch Record Reviewer Jobs (NOW HIRING)

New Cibo Vita LLC

Batch Records Technician

Totowa, NJ · On-site

$17/hr

Apply administrative and recordkeeping processes to support batch record document control * Committed to maintain excellent Food Safety Culture within the organization * Review production and QC ...

Kellton Tech

Quality Associate - Raleigh, NC

Raleigh, NC · On-site

$30 - $33/hr

... batch record review, release activities, and building trackers to enhance operational efficiency. This position requires strong attention to detail, familiarity with document management systems such ...

AstraZeneca

Quality Assurance Associate

Santa Monica, CA · On-site

$55K - $83K/yr

You will also be expected to independently coordinate and manage timelines for batch record reviews ... Well versed in various cell therapy manufacturing processes The annual base pay (or hourly rate of ...

CTK USA INC

QA Associate

Corona, CA · On-site

$18 - $26/hr

In this role, you'll handle change control, deviation and nonconformance documentation, reviewer-level batch record GMP compliance review, supplier audit support, training record management, and the ...

New

Abbott

Quality Assurance Specialist

Pomona, CA · On-site

$21 - $25/hr

Perform batch record review, record administration, and batch release activities. * Review and generate Certificates of Analysis (COA) and Certificates of Conformance (COC). * Manage and track Change ...

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How much do hourly batch record reviewer jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for hourly batch record reviewer in the United States is $20.34, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $21.15 per hour, depending on experience, location, and employer.

What is an hourly batch record reviewer?

Hourly Batch Record Reviewers are quality assurance professionals who examine manufacturing batch records on an hourly basis to ensure compliance with regulatory and company standards. Their main role is to review documentation for accuracy, completeness, and adherence to Good Manufacturing Practices (GMP). This helps prevent errors or deviations in the production process, ensuring that products are safe and meet quality requirements. Their work is critical in industries like pharmaceuticals, biotechnology, and food manufacturing, where strict documentation is essential.

What are some common challenges an hourly batch record reviewer may face during their shifts?

Hourly Batch Record Reviewers often manage tight deadlines to ensure all production documentation is reviewed and approved without delaying manufacturing processes. They must maintain high attention to detail to spot errors or omissions, as inaccuracies can impact product quality and regulatory compliance. Additionally, balancing communication with production staff and quality assurance teams is essential, as they often need to clarify discrepancies or gather additional information quickly. Adapting to shifting production priorities and handling repetitive tasks while maintaining accuracy are also frequent challenges.

What are the key skills and qualifications needed to thrive as an hourly batch record reviewer, and why are they important?

To thrive as an Hourly Batch Record Reviewer, you need strong attention to detail, knowledge of Good Manufacturing Practices (GMP), and a background in life sciences or a related field. Familiarity with electronic batch record systems, document management software, and quality control protocols is typically required. Excellent organizational skills, critical thinking, and effective communication help ensure errors are caught and compliance is maintained. These abilities are crucial for maintaining high product quality, meeting regulatory requirements, and supporting efficient manufacturing processes.

What is the difference between Hourly Batch Record Reviewer vs Quality Control Technician?

AspectHourly Batch Record ReviewerQuality Control Technician
CredentialsTypically requires a high school diploma or equivalent; some roles prefer certifications in GMP or QAUsually requires a high school diploma; certifications in quality control or laboratory techniques are common
Work EnvironmentPharmaceutical or manufacturing facilities, reviewing batch records during productionLaboratories or manufacturing sites, performing testing and inspections
Employer & IndustryPharmaceutical, biotech, or manufacturing companiesPharmaceutical, biotech, or manufacturing industries

Both roles are essential in manufacturing settings, focusing on quality assurance. The Hourly Batch Record Reviewer primarily reviews documentation during production, while the Quality Control Technician conducts testing and inspections to ensure product quality. Understanding these differences helps in choosing the right career path or job search focus.

What cities are hiring for Hourly Batch Record Reviewer jobs?

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What are the most commonly searched types of Batch Record Reviewer jobs?

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Hourly Batch Record Reviewer jobs near you

Specialist QA-Drug Substance

Juncos, PR • On-site

BioPharma Consulting JAD Group
Biotechnology Research and Development • 51 - 200 employees
Learn more about BioPharma Consulting JAD Groupexternal

Contractor

Posted 3 days ago

New

Job description

This position supports operations through accurate Batch Record Review, documentation compliance, electronic systems management, inventory control, and timely operational decision‑making. Requires strong GMP understanding, ability to manage multiple priorities, and capability to work independently.

Functions

  • Perform comprehensive Batch Record Review for completeness, accuracy, compliance, and adherence to procedures and GMP.
  • Review and approve product MPs.
  • Approve process validation protocols and reports for manufacturing processes.
  • Approve Environmental Characterization reports.
  • Approve planned incidents.
  • Review manufacturing documentation for GDP, data integrity, accuracy, traceability, and compliance.
  • Use SAP for inventory activities: material verification, transactions, reconciliation, status review, and manufacturing support.
  • Utilize PAX / Electronic Batch Record (eBR) systems to review and support electronic documentation workflows.
  • Participate in DAI meetings and other Quality/operational forums; present information, identify risks, communicate pending items, and support timely decisions.
  • Review and approve Work Orders.
  • Review and approve EMS/BMS alarms.
  • Approve NC investigations and CAPA records.
  • Approve change controls.
  • Provide lot disposition and authorize lots for shipment.
  • Own site quality program procedures.
  • Serve as designee for QA Manager on local CCRB.
  • Lead investigations.
  • Lead site audits.
  • Review Risk Assessments.
  • Review equipment/system Root Cause Analysis investigations and support trend evaluations.
  • Request Quality participation on incident triage team.
  • Represent QA on NPI teams.
  • Support automation activities.
  • Support facilities and environmental programs.
  • Collaborate with higher‑level external resources as needed.

Skills

  • Strong project management skills.
  • Excellent organizational skills with ability to follow assignments through completion.
  • Ability to initiate and lead cross‑functional teams.
  • Strong influencing and negotiation skills.
  • Deep knowledge in area of expertise.
  • Strong understanding of manufacturing, distribution, QA, QAL, validation, and process development processes.
  • Ability to interact effectively with regulatory agencies.
  • Proficiency in word processing, presentation, database, and spreadsheet applications.
  • Strong written and oral communication, facilitation, and presentation skills.
  • Ability to work independently and interact effectively across organizational levels.
  • Advanced data trending and evaluation skills.
  • Ability to evaluate compliance issues.

Requirements

  • Doctorate OR
  • Master’s + 2 years of directly related experience OR
  • Bachelor’s + 4 years of directly related experience OR
  • Associate’s + 8 years of directly related experience OR
  • High School/GED + 10 years of directly related experience.

Preferred Qualifications (must have)

  • Batch Record Review
  • GMP / GDP Documentation
  • SAP Inventory Management
  • PAX / Electronic Batch Records (eBR)
  • Manufacturing and Quality Systems
  • Inventory reconciliation & material traceability
  • Quality event assessment & escalation
  • Data Integrity principles

Benefits

  • 9-month contract with possible extension
  • 3rd Shift (10:00PM- 6:30 AM)