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Hourly Batch Record Reviewer Jobs (NOW HIRING)

Avid Bioservices

Batch Record Coordinator

Tustin, CA · On-site

$16.68 - $22.26/hr

Reviews executed batch records for completeness, accuracy, and adherence to ALCOA principles ... The compensation range for this role is $16.68 to $22.26 hourly depending on experience and ...

Avid Bioservices

Batch Record Coordinator

Tustin, CA · On-site

$16.68 - $22.26/hr

Reviews executed batch records for completeness, accuracy, and adherence to ALCOA principles ... The compensation range for this role is $16.68 to $22.26 hourly depending on experience and ...

Avid Bioservices

Batch Record Coordinator

Tustin, CA · On-site

$16.68 - $22.26/hr

Reviews executed batch records for completeness, accuracy, and adherence to ALCOA principles ... The compensation range for this role is $16.68 to $22.26 hourly depending on experience and ...

INCOG

QA Batch Review Specialist

Fishers, IN · On-site

Full lifecycle review and disposition of parenteral manufacturing Batch Records (Formulation, Filling, Inspection, & Packaging) for Media Fills and Drug Product. Provide Client access and support in ...

INCOG

Senior QA Batch Disposition Specialist

Fishers, IN · On-site

$77K - $106K/yr

Lead full lifecycle review and disposition of parenteral manufacturing batch records (Formulation, Filling, Inspection, and Packaging) for Media Fills and Drug Product across all production stages.

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How much do hourly batch record reviewer jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for hourly batch record reviewer 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 is an hourly batch record reviewer?

Hourly Batch Record Reviewers are quality assurance professionals who examine manufacturing batch records on an hourly basis to ensure compliance with regulatory and company standards. Their main role is to review documentation for accuracy, completeness, and adherence to Good Manufacturing Practices (GMP). This helps prevent errors or deviations in the production process, ensuring that products are safe and meet quality requirements. Their work is critical in industries like pharmaceuticals, biotechnology, and food manufacturing, where strict documentation is essential.

What are some common challenges an hourly batch record reviewer may face during their shifts?

Hourly Batch Record Reviewers often manage tight deadlines to ensure all production documentation is reviewed and approved without delaying manufacturing processes. They must maintain high attention to detail to spot errors or omissions, as inaccuracies can impact product quality and regulatory compliance. Additionally, balancing communication with production staff and quality assurance teams is essential, as they often need to clarify discrepancies or gather additional information quickly. Adapting to shifting production priorities and handling repetitive tasks while maintaining accuracy are also frequent challenges.

What are the key skills and qualifications needed to thrive as an hourly batch record reviewer, and why are they important?

To thrive as an Hourly Batch Record Reviewer, you need strong attention to detail, knowledge of Good Manufacturing Practices (GMP), and a background in life sciences or a related field. Familiarity with electronic batch record systems, document management software, and quality control protocols is typically required. Excellent organizational skills, critical thinking, and effective communication help ensure errors are caught and compliance is maintained. These abilities are crucial for maintaining high product quality, meeting regulatory requirements, and supporting efficient manufacturing processes.

What is the difference between Hourly Batch Record Reviewer vs Quality Control Technician?

AspectHourly Batch Record ReviewerQuality Control Technician
CredentialsTypically requires a high school diploma or equivalent; some roles prefer certifications in GMP or QAUsually requires a high school diploma; certifications in quality control or laboratory techniques are common
Work EnvironmentPharmaceutical or manufacturing facilities, reviewing batch records during productionLaboratories or manufacturing sites, performing testing and inspections
Employer & IndustryPharmaceutical, biotech, or manufacturing companiesPharmaceutical, biotech, or manufacturing industries

Both roles are essential in manufacturing settings, focusing on quality assurance. The Hourly Batch Record Reviewer primarily reviews documentation during production, while the Quality Control Technician conducts testing and inspections to ensure product quality. Understanding these differences helps in choosing the right career path or job search focus.

What cities are hiring for Hourly Batch Record Reviewer jobs?

Cities with the most Hourly Batch Record Reviewer job openings:

What are the most commonly searched types of Batch Record Reviewer jobs?

The most popular types of Batch Record Reviewer jobs are:

What states have the most Hourly Batch Record Reviewer jobs?

States with the most job openings for Hourly Batch Record Reviewer jobs include:

Hourly Batch Record Reviewer jobs near you

Night Shift QA Batch Record Reviewer/ Person in Plant, 4553936

Artech Information System LLC

San Carlos, CA • On-site

Contractor

Re-posted 25 days ago

Job description

Company Description

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.

Job Description

Pharmaceuticals located in San Carlos is seeking a Quality Assurance Batch Record Reviewer / Person-In-Plant to support Quality oversight of manufacturing operations for the NIGHT SHIFT. This is a temporary assignment. Responsible for on-the-floor, timely and effective GMP review and production close-out of batch record documentation in order to maintain a continuous flow of batch records

Single point of contact in the plant during the assigned Manufacturing shift for the Batch Record Review Process and Quality matters.


Operates on a 8-hour shift (10:00pm-6:30am) to support 24x5 Operations. 

Responsibilities include approval and issuance of batch records, approving records; issue resolution; batch record review.

Reviews batch documentation for accuracy and completeness according to cGMP's to ensure timely release.

Supports/performs scanning of records for uploading into share folders

Conducts QA Person-In-Plant activities including, Area Approval, Line Clearance Approval, Batch Record Review, Deviation triage and preliminary investigation, etc.

Assists with Deviation investigations, Compliance investigations, and Customer complaint investigations.

Supports implementation of CAPAs, SOP revisions, Quality improvement initiatives, Operational Excellence projects, etc.

Adheres to internal/external Guidelines, Specifications and Regulatory requirements while reviewing batch documentation.

Ensures all GMP's, SOP's and protocols are followed.

Positively interacts with internal associates to quickly and effectively resolve issues.

Addresses deficiencies and ensures completion of follow-up actions, specifically those that target process fixes to maintain consistent resolutions to batch review issues according to GMP standards and Novartis objectives.


Skills:  

Minimum Requirements: MUST BE ABLE TO WORK NIGHT SHIFT 10:00pm-6:30am. First couple weeks of training will be day shift.

2-5 years related manufacturing or quality experience. BS degree in science in preferred.

Demonstrated cGMP knowledge and experience.

Strong interpersonal, written, communication, and problem solving skills.

Must be well organized, flexible and able work with minimal supervision.

Prior experience with Quality Assurance Batch Record Review and/or Person-In-Plant is preferred.

Strong background and skills in Quality, Manufacturing, communication and computer related systems are preferred.

Experience with Deviation Investigations and Root Cause Analysis is a plus.

Experience with Microsoft Word / Excel, SAP and TrackWise is a plus.


Qualifications

BS degree in science is preferred.

Additional Information

For more information, please contact

Akriti Gupta

(973) 967-3409

Morristown, NJ 07960 


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About Artech

Sourced by ZipRecruiter

Artech is a leading IT staffing and consulting company based in Morristown, NJ, US. Since its foundation in 1992, Artech has mastered in complementing human expertise with technology and business acumen to produce world-class staffing solutions. The company caters to diverse industry sectors, including financial services, healthcare, telecommunication, energy and utilities, supply chain, and retail. It provides IT consulting, project management, professional and staff augmentation, and managed staffing services. Artech's mission is to provide exceptional IT staffing services to its clients by comprehending their business needs and then crafting a customized staffing strategy. Its notable achievement includes being recognized as one of the largest IT staffing companies in the U.S, according to Staffing Industry Analysts (SIA).

Industry

Recruiting and staffing services

Company size

10,000+ Employees

Headquarters location

Morristown, NJ, US

Year founded

1992

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