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Batch Record Review Jobs (NOW HIRING)

Alan Baird Industries

Batch Record Reviewer

Allendale, NJ · On-site

$19 - $22/hr

Review batch records and travelers for completeness, accuracy, and compliance. * Release product in accordance with internal procedures and quality standards. * Ensure all documentation adheres to ...

Nitto Denko Corp.

$73K - $89K/yr

As a Quality Assurance Specialist III, you will be responsible for being a lead QA representative for Raw Materials and Batch Records functions. Key Responsibilities: * Review and verify raw material ...

Avid Bioservices

Batch Record Coordinator

Tustin, CA

$16.68 - $22.26/hr

You'll compile and review data, support manufacturing activity planning, and swiftly resolve issues. Coordinate controlled documents, training packets, and batch record preparation, while also ...

Avid Bioservices

Batch Record Coordinator

Tustin, CA · On-site

$16.68 - $22.26/hr

You'll compile and review data, support manufacturing activity planning, and swiftly resolve issues. Coordinate controlled documents, training packets, and batch record preparation, while also ...

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How much do batch record review jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for batch record review 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 are common challenges faced in a batch record review role, and how can they be addressed?

One common challenge in a Batch Record Review role is ensuring the completeness and accuracy of documentation while working under tight deadlines, as production schedules often depend on timely batch release. Attention to detail is critical, since even minor discrepancies can lead to delays or compliance issues. Effective communication and collaboration with production, quality assurance, and laboratory teams are key to resolving discrepancies quickly. Proactively staying updated on current Good Manufacturing Practices (cGMP) and internal protocols can also help minimize errors and streamline the review process.

What is a batch record reviewer?

A Batch Record Reviewer is a quality assurance professional responsible for reviewing and verifying production batch records in pharmaceutical or manufacturing environments. Their main role is to ensure that all documentation related to the production of each batch complies with regulatory standards and company procedures. This includes checking for accuracy, completeness, and compliance with Good Manufacturing Practices (GMP). By doing so, they help maintain product quality and safety before products are released to the market.

What is the difference between Batch Record Review vs Quality Control Analyst?

AspectBatch Record ReviewQuality Control Analyst
Primary RoleReview and approve manufacturing batch records for compliance and accuracyPerform testing and analysis of raw materials, in-process, and finished products
CertificationsOften requires GMP, cGMP, or industry-specific certificationsRequires laboratory certifications, such as ASQ or equivalent
Work EnvironmentManufacturing or production facilities, quality assurance departmentsLaboratories, quality control labs, manufacturing sites
Industry UsagePharmaceutical, biotech, and manufacturing sectorsPharmaceutical, biotech, and food industries

While both roles focus on quality, Batch Record Review primarily involves reviewing manufacturing documentation for compliance, whereas Quality Control Analysts conduct testing and analysis to ensure product quality. Both are essential in regulated industries and often collaborate to maintain product standards.

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

To thrive as a Batch Record Reviewer, you need strong attention to detail, knowledge of Good Manufacturing Practices (GMP), and experience in pharmaceutical or biotechnology documentation, often supported by a degree in life sciences or related fields. Familiarity with electronic document management systems (EDMS), quality management software, and regulatory compliance tools is typically required. Excellent analytical skills, organization, and effective communication are standout soft skills for this role. These abilities ensure the accuracy, compliance, and completeness of batch records, which are critical for product quality and regulatory approval.
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Batch Record Review jobs near you
Infographic showing various Batch Record Review job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, and 4% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $42,304 per year, or $20.3 per hour.

Quality Specialist III, Batch Record Review

Thermo Fisher Scientific

Greenville, NC • On-site

Full-time

Re-posted 27 days ago

Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 422 frontline employees who took The Breakroom Quiz

196th of 537 rated manufacturers

Job description

Work Schedule
First Shift (Days)
Environmental Conditions
Able to lift 40 lbs. without assistance, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
About Thermo Fisher Scientific
As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Our Mission is to enable our customers to make the world healthier, cleaner and safer. We support our colleagues with the resources needed to achieve individual career goals while advancing solutions to some of the world's toughest challenges.
About the Business
Our Pharma Services Group (PSG) is a global leader in integrated drug development and manufacturing solutions for pharmaceutical and biotech companies. The Greenville, NC site specializes in sterile and oral solid dose (OSD) manufacturing, supported by advanced technologies and a collaborative, quality-focused environment.
Discover Impactful Work
The Quality Assurance Specialist III - Batch Release plays a critical role in ensuring that manufactured products meet all quality and regulatory requirements prior to release. This position supports site-wide batch disposition activities, with a strong focus on sterile/aseptic manufacturing processes. You will partner cross-functionally to ensure compliance with GMP standards while driving timely and accurate batch review and release.
A Day in the Life
• Perform comprehensive batch record review to support product release in compliance with GMP and regulatory requirements
• Ensure all documentation, deviations, and investigations are complete, accurate, and aligned with quality standards
• Collaborate with Manufacturing, Quality Control, and other cross-functional teams to resolve batch-related issues
• Evaluate deviations, change controls, and CAPAs for impact on product quality and release decisions
• Support inspection readiness and participate in internal and external audits
• Communicate effectively across all organizational levels to ensure alignment on quality expectations
• Contribute to continuous improvement initiatives within the Quality organization
Keys to Success
Education & Experience
• Bachelor's degree in Life Sciences, Chemistry, Engineering, or related field required
• Minimum 5 years of Quality Assurance experience in a regulated pharmaceutical environment
• Required: Experience with sterile/aseptic manufacturing and batch release activities
Knowledge, Skills & Abilities
• Strong knowledge of GMP/GxPregulations and quality systems
• Proven experience in batch record review and product disposition
• Familiarity with deviation management, CAPA, and change control processes
• Strong investigation and root cause analysis capabilities
• Excellent attention to detail and documentation skills
• Effective written and verbal communication skills across all levels
• Ability to work both independently and collaboratively in a team environment
• Proficiency with quality systems (e.g., TrackWise) and Microsoft Office
Working Conditions
Standard Monday-Friday business hours
Work performed in both office and manufacturing environments requiring appropriate PPE
Why Join Us?
You will be part of a high-performing Quality team supporting critical pharmaceutical manufacturing operations. This role offers the opportunity to directly impact patient safety and product quality while working in a collaborative and growth-oriented environment.

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