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Contract Qa Batch Record Review Jobs in Raleigh, NC

Kellton Tech

Quality Associate - Raleigh, NC

Raleigh, NC · On-site

$30 - $33/hr

Raleigh, NC Duration: 12 months contract with possible extension Pay rate range: $30/hr-$33/hr Job ... Quality Assurance in an FDA-regulated industry. Experience with batch record review, document ...

Kelly Services

Sr QA Operations Manager

Raleigh, NC · On-site

$175K/yr

The QA Operations Sr. Manager provides quality leadership and oversight across site operations ... Oversee batch record review and product disposition processes. * Ensure robust review processes ...

Guerbet

QA Operations Sr. Manager

Raleigh, NC · On-site

$90 - $120/hr

The QA Operations Sr. Manager provides quality leadership and oversight across site operations ... Oversee batch record review and product disposition processes. * Ensure robust review processes ...

UPL Limited

Quality Engineer (Chemical)

Cary, NC · On-site

$66K - $86K/yr

Position Summary The Quality Assurance (QA) Engineer is responsible for ensuring that agrochemical ... Review and approve batch records, specifications, SOPs, and quality documentation. * Lead ...

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All JobsContract Qa Batch Record Review JobsContract Qa Batch Record Review Jobs in Raleigh, NC

Contract Qa Batch Record Review information

See Raleigh, NC salary details

$12

$28

$60

How much do contract qa batch record review jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for contract qa batch record review in Raleigh, NC is $28.47, according to ZipRecruiter salary data. Most workers in this role earn between $18.22 and $33.41 per hour, depending on experience, location, and employer.

What is a contract QA batch record reviewer?

A Contract QA Batch Record Reviewer is a quality assurance professional who is hired on a contract basis to review and verify manufacturing batch records in industries like pharmaceuticals, biotechnology, or food production. Their main responsibility is to ensure that all production documentation complies with regulatory standards and company protocols before products are released. This role involves checking for accuracy, completeness, and consistency in records, identifying any discrepancies or deviations, and working with production teams to resolve issues. Contract-based reviewers may work with multiple clients and help ensure that all batches meet strict quality and safety requirements.

What are the key skills and qualifications needed to thrive as a contract QA batch record reviewer, and why are they important?

To thrive as a Contract QA Batch Record Reviewer, you need a solid understanding of GMP regulations, pharmaceutical manufacturing processes, and experience with batch record documentation, often supported by a degree in life sciences or a related field. Familiarity with quality management systems (QMS), electronic batch record (EBR) systems, and regulatory compliance tools is typically required. Attention to detail, analytical thinking, and effective communication are crucial soft skills for identifying discrepancies and ensuring compliance. These competencies are vital for maintaining product quality, regulatory adherence, and minimizing production risks in pharmaceutical environments.

What are some common challenges faced in a contract QA batch record review role, and how can they be managed?

In a Contract QA Batch Record Review position, one of the most common challenges is managing tight deadlines while ensuring meticulous attention to detail. Batch records often contain complex information, and discrepancies or omissions must be identified and addressed promptly to maintain compliance with regulatory standards. Effective communication with production and quality teams is crucial for resolving issues quickly. Staying organized, prioritizing tasks, and maintaining up-to-date knowledge of relevant regulations can help streamline the review process and minimize errors.

What is the difference between Contract Qa Batch Record Review vs Contract Quality Assurance Specialist?

AspectContract Qa Batch Record ReviewContract Quality Assurance Specialist
CertificationsGMP, GDP, ISO training, QA certificationsGMP, GDP, ISO training, QA certifications
Work EnvironmentPharmaceutical/biotech manufacturing, quality control labsPharmaceutical/biotech manufacturing, quality assurance departments
Primary ResponsibilitiesReviewing batch records for compliance, documentation accuracyOverseeing quality systems, audits, process validation

The Contract Qa Batch Record Review focuses specifically on reviewing batch documentation for compliance and accuracy during manufacturing. In contrast, the Contract Quality Assurance Specialist has broader responsibilities, including overseeing quality systems and conducting audits. Both roles require GMP knowledge and work within pharmaceutical or biotech environments, but the Batch Record Review is more task-specific, while the QA Specialist has a wider scope of quality management.

What are the most commonly searched types of Qa Batch Record Review jobs in Raleigh, NC?

The most popular types of Qa Batch Record Review jobs in Raleigh, NC are:

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

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The top searched job categories for Contract Qa Batch Record Review jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Contract Qa Batch Record Review jobs?

Cities near Raleigh, NC with the most Contract Qa Batch Record Review job openings:

Contract Qa Batch Record Review jobs near you
Infographic showing various Contract Qa Batch Record Review job openings in Raleigh, NC as of June 2026, with employment types broken down into 1% Internship, 27% Full Time, 68% Part Time, 2% Temporary, 1% Contract, and 1% Nights. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $59,224 per year, or $28.5 per hour.

Quality Specialist - Batch Record Review

Equiliem

Raleigh, NC

$22 - $24/hr

Full-time

Posted 8 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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