1

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

... 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 ...

QA Specialist (Hybrid)

Raleigh, NC · Hybrid

$66K - $86K/yr

This role contributes to batch record review, documentation management, investigation support, and quality system activities to ensure compliance with cGMPs, internal procedures, and regulatory ...

QA Specialist (Hybrid)

Raleigh, NC · On-site

$66K - $86K/yr

This role contributes to batch record review, documentation management, investigation support, and quality system activities to ensure compliance with cGMPs, internal procedures, and regulatory ...

Oversee batch record review and product disposition processes. * Ensure robust review processes support compliant and timely product release. * Assess and address quality issues impacting batch ...

Oversee batch record review and product disposition processes. * Ensure robust review processes support compliant and timely product release. * Assess and address quality issues impacting batch ...

next page

Showing results 1-20

Batch Record Reviewer information

See Raleigh, NC salary details

$12

$19

$32

How much do batch record reviewer jobs pay per hour?

As of Jul 31, 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 are the key skills and qualifications needed to thrive in the Batch Record Reviewer position, and why are they important?

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 is a Batch Record Reviewer job?

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 typical day look like for a Batch Record Reviewer, and who do they collaborate with most often?

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 cities near Raleigh, NC are hiring for Batch Record Reviewer jobs? Cities near Raleigh, NC with the most Batch Record Reviewer job openings:
Infographic showing various Batch Record Reviewer job openings in Raleigh, NC as of July 2026, with employment types broken down into 33% Full Time, and 67% Contract. Highlights an 100% In-person job distribution, with an average salary of $41,123 per year, or $19.8 per hour.

Quality Associate - Raleigh, NC

Kellton Tech

Raleigh, NC • On-site

$30 - $33/hr

Contractor

Re-posted 19 days ago


Job description

Title: Quality Associate
Location: Raleigh, NC
Duration: 12 months contract with possible extension
Pay rate range: $30/hr-$33/hr
 
Job Summary
The Contractor Quality Associate, Biologics will play a key role in supporting data migration, 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 as Veeva Vault, and proficiency in Excel. Experience in Quality Assurance is essential, and knowledge of Power BI is preferred to support data visualization and reporting. The associate will collaborate with cross-functional teams to ensure accurate documentation, timely release of batches, and development of tools to monitor key performance indicators.
The position requires familiarity with Veeva Vault or similar document management systems and Power BI. While Power BI proficiency is preferred, it is not a mandatory requirement for the role.
 
Essential Functions
Lead and manage the migration of quality documents into Veeva Vault, ensuring accuracy and compliance with documentation standards.
Support the transition of legacy records into Veeva, maintaining traceability and completeness.
Build and maintain trackers to monitor key performance indicators (KPIs), batch record status, and release metrics.
Assist in batch record reviews to ensure documentation is complete, compliant, and ready for release.
Support release activities by coordinating documentation readiness and collaborating with QA team members and cross functional teams.
 
Requirements
Education:
Associate degree (required); BS/BA in pertinent life sciences or closely related field (preferred)
Technical:
3+ years of pharmaceutical/biotech working experience in Quality Assurance in an FDA-regulated industry.
Experience with batch record review, document control, and release processes.
Familiarity with SAP inventory system.
Proficient in Microsoft Office tools, and Veeva Quality systems.