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Batch Record Reviewer Jobs in Raleigh, NC (NOW HIRING)

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 ...

AA2IT

Documentation Specialist

Durham, NC · On-site

$29.50/hr

Provide documentation support for vaccine production activities Review batch record, logbooks and electronic logbooks for errors and partner with Production, Quality and other personnel to correct ...

Indivior PLC

MQA Specialist - 3rd Shift

Raleigh, NC · On-site

$64K - $81K/yr

The MQA Specialist will work closely with production personnel to complete in-process batch record review, resolve batch related issues, and ensure proper good documentation practices. In addition ...

Indivior

MQA Specialist - 3rd Shift

Raleigh, NC

$81/hr

The MQA Specialist will work closely with production personnel to complete in-process batch record review, resolve batch related issues, and ensure proper good documentation practices. In addition ...

Indivior PLC

MQA Specialist - 3rd Shift

Raleigh, NC · On-site

The MQA Specialist will work closely with production personnel to complete in-process batch record review, resolve batch related issues, and ensure proper good documentation practices. In addition ...

Avacone

MES / PAS-X MBR Designer

Durham, NC · On-site

$149K/yr

Review and assess process documentation, batch records, manufacturing instructions, and other source materials required for MBR design. * Perform fit-gap assessments against the Global MES Template ...

Avacone

MES / PAS-X MBR Designer

Durham, NC · On-site

$140K/yr

Review and assess process documentation, batch records, manufacturing instructions, and other source materials required for MBR design. * Perform fit-gap assessments against the Global MES Template ...

Socket.dev

MES / PAS-X MBR Designer

Durham, NC · On-site

$18.50 - $22.75/hr

Review and assess process documentation, batch records, manufacturing instructions, and other source materials required for MBR design. * Perform fit-gap assessments against the Global MES Template ...

Avacone

MES / PAS-X MBR Designer

Durham, NC · On-site

$149K/yr

Review and assess process documentation, batch records, manufacturing instructions, and other source materials required for MBR design. * Perform fit-gap assessments against the Global MES Template ...

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All JobsBatch Record Reviewer JobsBatch Record Reviewer Jobs in Raleigh, NC

Batch Record Reviewer information

See Raleigh, NC salary details

$12

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How much do batch record reviewer jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for batch record reviewer in Raleigh, NC is $19.77, according to ZipRecruiter salary data. Most workers in this role earn between $16.83 and $20.58 per hour, depending on experience, location, and employer.

What is a batch record reviewer?

A Batch Record Reviewer is responsible for reviewing manufacturing and production records to ensure compliance with regulatory standards and internal quality procedures. They verify that all documentation is complete, accurate, and meets Good Manufacturing Practices (GMP) requirements. Their role helps maintain product quality and ensures that any discrepancies or deviations are identified and addressed before product release. Batch Record Reviewers typically work in industries such as pharmaceuticals, biotechnology, and food manufacturing.

What does a batch record reviewer do?

A typical day for a Batch Record Reviewer involves meticulously examining batch records, manufacturing documentation, and supporting data to ensure compliance with regulatory and company standards. Reviewers frequently interact with production staff, quality assurance teams, and sometimes laboratory personnel to clarify discrepancies or gather additional information. Attention to evolving priorities and deadlines is common, especially when batches are ready for product release. This role offers valuable exposure to multiple departments and can serve as an excellent pathway to higher-level quality or regulatory positions within the company.

What skills and qualifications are needed to be a batch record reviewer?

To thrive as a Batch Record Reviewer, you need a keen attention to detail, strong analytical skills, and a solid understanding of Good Manufacturing Practices (GMP), often supported by a degree in life sciences or related fields. Familiarity with electronic documentation systems, quality management software, and sometimes certifications like Six Sigma or GMP training is highly valued. Excellent organization, communication, and problem-solving abilities are important soft skills for ensuring thorough and compliant record review. These competencies are crucial for maintaining product quality, regulatory compliance, and operational efficiency in pharmaceutical or biotech manufacturing environments.

What are popular job titles related to Batch Record Reviewer jobs in Raleigh, NC?

For Batch Record Reviewer jobs in Raleigh, NC, the most frequently searched job titles are:

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The top searched job categories for Batch Record Reviewer jobs in Raleigh, NC are:

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Batch Record Reviewer jobs near you
Infographic showing various Batch Record Reviewer job openings in Raleigh, NC as of September 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, and 3% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $41,123 per year, or $19.8 per hour.

Quality Specialist - Batch Record Review

Raleigh, NC

Equiliem
Recruiting and Staffing Services • 1 - 5K employees
Learn more about Equiliemexternal

$22 - $24/hr

Full-time

Posted 14 days ago

Job description

Quality Specialist II - Batch Record Review 
Raleigh, NC 
Pay: $22.00 - $24.00 per hour 
26-07733
Job Summary

The Quality Specialist II – Batch Record Review is responsible for reviewing manufacturing and packaging batch records to ensure compliance with current Good Manufacturing Practices (cGMP), internal quality standards, and regulatory requirements. This role supports product release activities by verifying production documentation, identifying discrepancies, and collaborating with Manufacturing and Quality teams to ensure accurate and compliant records. The position also supports quality systems, facility inspections, material status verification, and continuous improvement initiatives within a regulated manufacturing environment.

Job Responsibilities

  • Review manufacturing and packaging batch records for completeness, accuracy, and compliance with cGMP requirements, SOPs, and internal quality standards.
  • Verify that critical manufacturing steps, in-process inspections, reconciliations, and production documentation have been completed accurately.
  • Identify documentation discrepancies, omissions, or errors and coordinate timely resolution with Manufacturing and Quality teams.
  • Support product disposition activities by assessing batch documentation and escalating quality concerns as needed.
  • Retrieve production batch records for review and return completed documentation following approval.
  • Scan, organize, and maintain batch records in accordance with documentation and data integrity requirements.
  • Assist with investigations involving deviations, nonconformances, and Corrective and Preventive Actions (CAPAs) related to production documentation.
  • Verify identification and status labeling of raw materials, intermediates, and in-process materials.
  • Conduct inspections of manufacturing equipment, production areas, and materials to ensure compliance with quality standards.
  • Support inventory status control activities, including quarantine, approved, and rejected materials.
  • Assist with facility compliance activities, including pest control program support and vendor documentation review.
  • Provide guidance to production personnel on proper batch record documentation practices.
  • Participate in continuous improvement initiatives to enhance quality processes and regulatory compliance.
  • Maintain organized quality documentation and perform additional Quality Assurance responsibilities as assigned.

Job Requirements

  • Minimum of 1–3 years of Quality Assurance experience in a pharmaceutical, biotechnology, medical device, or other regulated manufacturing environment.
  • Associate degree in a scientific, technical, or related discipline required.
  • Experience performing end-of-process Quality Assurance activities; Quality Control experience alone is not sufficient.
  • Experience reviewing and scanning manufacturing batch records.
  • Working knowledge of current Good Manufacturing Practices (cGMP).
  • Proficiency with Microsoft Word and Excel.
  • Strong attention to detail and documentation accuracy.
  • Excellent organizational, verbal, and written communication skills.
  • Ability to manage multiple priorities and meet deadlines.

Education

  • Associate degree in a scientific, technical, or related discipline required.

Work Experience

  • 1–3 years of experience in Quality Assurance within a regulated manufacturing environment.
  • Previous batch record review experience in pharmaceutical manufacturing preferred.
  • Experience supporting deviations, CAPAs, investigations, or quality systems preferred.
  • Familiarity with FDA-regulated manufacturing environments and data integrity principles preferred. #ZR
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About Equiliem

Sourced by ZipRecruiter

Equiliem specializes in staffing clinical, non-clinical, and allied personnel. We excel in all levels, disciplines, and specialties within the healthcare spectrum. Our projects range from short to long term local and travel assignments. Equiliem has been recognized as a certified small business enterprise. In addition, we are proud that we have earned the prestigious Joint Commission accreditation for staffing firms and have been awarded Best in Staffing 4 years running by our employees and client partners.

Industry

Recruiting and staffing services

Company size

1,001 - 5,000 Employees

Headquarters location

East Brunswick, NJ, US

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