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Assistant Qa Batch Record Review Jobs (NOW HIRING)

QA Specialist II - Lot Review Location: This position is based in our Portsmouth, NH office. The ... Perform detailed review of manufacturing batch records and supporting documentation for ...

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 ...

QA Specialist (Hybrid)

Raleigh, NC · On-site

$66K - $86K/yr

This role contributes to batch record review, documentation management, investigation support, and ... and completeness. * Assist in the development, implementation, and maintenance of quality ...

Quality Assurance Reporting To: QA Manager / QA Director Responsible For (Staff): No The QA ... Primary responsibilities for this role includes Batch Record Review, Lot Disposition, and Quality ...

Analyst, QA

North Chicago, IL · On-site

$65K/yr

The QA Analyst supports the Quality Manager in the execution and oversight of the Quality System ... Reviews batch release documentation and batch records to support product disposition and shipment ...

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Assistant Qa Batch Record Review information

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

As of Aug 6, 2026, the average hourly pay for assistant qa batch record review in the United States is $21.99, according to ZipRecruiter salary data. Most workers in this role earn between $18.75 and $24.52 per hour, depending on experience, location, and employer.

What is the difference between Assistant Qa Batch Record Review vs Quality Control Technician?

AspectAssistant Qa Batch Record ReviewQuality Control Technician
CredentialsTypically requires a degree in life sciences or related fieldOften requires a degree or certification in quality control or laboratory sciences
Work EnvironmentMostly office-based, reviewing batch records and documentationLaboratory or manufacturing setting, performing tests and inspections
Industry UsageCommonly used in pharmaceutical and biotech industries for documentation reviewUsed across manufacturing, testing, and quality assurance in similar industries

The Assistant Qa Batch Record Review primarily focuses on reviewing and ensuring the accuracy of batch documentation, often working in an office environment. In contrast, the Quality Control Technician performs hands-on testing and inspections in laboratory or manufacturing settings. Both roles are essential in maintaining product quality and compliance within the pharmaceutical and biotech industries.

What cities are hiring for Assistant Qa Batch Record Review jobs? Cities with the most Assistant Qa Batch Record Review job openings:
What are the most commonly searched types of Qa Batch Record Review jobs? The most popular types of Qa Batch Record Review jobs are:
Infographic showing various Assistant Qa 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 $45,740 per year, or $22 per hour.

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

Artech Information System LLC

San Carlos, CA

Contractor

Re-posted 10 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 



Artech logo

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