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Batch Record Review Jobs (NOW HIRING)

Lonza

QA Specialist II-Lot review

Portsmouth, NH · On-site

Perform detailed review of manufacturing batch records and supporting documentation for completeness, accuracy, and compliance * Identify discrepancies, documentation errors, and GMP issues, and ...

Lonza

QA Specialist II-Lot review

Portsmouth, NH

Perform detailed review of manufacturing batch records and supporting documentation for completeness, accuracy, and compliance * Identify discrepancies, documentation errors, and GMP issues, and ...

Intellectt INC

QA / QC Inspector

Milpitas, CA · On-site

Batch record/lot history record review experience. Proficiency with Excel and SharePoint for data/document management. Strong communication and teamwork skills. Detail-oriented with auditing/document ...

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Batch Record Review information

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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 Assurance Associate - MQA

Tailstorm Health Inc

Phoenix, AZ • On-site

$45K/yr

Full-time

Re-posted 2 days ago

Job description

About Medivant Healthcare

Medivant Healthcare manufactures high‑quality sterile injectable medications at its FDA‑inspected facilities. The company is committed to strong quality systems, regulatory compliance, and delivering safe and effective products.

Position Summary

The Associate / Senior Associate – MQA supports documentation control, batch record review, sampling activities, material releases, investigations, and manufacturing quality oversight. This role ensures compliance with cGMP requirements and supports daily quality operations across production and packaging.

Key Responsibilities

• Upload documents into the Document Management System (DMS – MasterControl or equivalent).

• File and archive documents while maintaining tracking records for timely retrieval and archival.

• Review and release incoming materials in accordance with the Approved Vendor List and Certificate of Analysis requirements.

• Issue controlled documents and logbooks to all departments.

• Perform AQL inspections as required.

• Conduct line clearances, in‑process sampling, and finished‑product sampling for manufacturing and packaging operations.

• Prepare Master Batch Manufacturing Records (MBMRs) and review executed Batch Manufacturing Records (BMRs).

• Pull, label, and store product samples after manufacturing.

• Support product and material destruction processes.

• Participate in failure investigations and support documentation.

• Review label printing activities for accuracy and compliance.

• Perform any additional duties assigned by the Department Head or designee.

Qualifications

Required:

• Bachelor’s degree in Pharmacy, Biotechnology, Chemistry, or related scientific discipline.

• 1-2 years of experience in pharmaceutical QA or manufacturing quality assurance roles.

• Knowledge of cGMP, documentation practices, sampling procedures, and material release processes.

• Strong attention to detail, documentation accuracy, and organizational skills.

Preferred:

• Experience in sterile manufacturing or injectable facilities.

• Experience with MasterControl or similar electronic documentation systems.

• Familiarity with batch record review and AQL inspection processes.

Work Environment & Physical Requirements

• Full‑time onsite role requiring presence in production and packaging areas.

• May require extended standing, gowning, and movement between controlled environments.

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