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 ...
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 ...
Batch Record Specialist
Bloomington, IN · On-site
This role will be responsible for reviewing executed batch records and manufacturing documentation to ensure compliance with cGMP requirements, regulatory standards, and internal procedures. The ...
Quick apply
Batch Record Specialist
Bloomington, IN · On-site
This role will be responsible for reviewing executed batch records and manufacturing documentation to ensure compliance with cGMP requirements, regulatory standards, and internal procedures. The ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
Manufacturing Batch Record Coordinator
$57K - $107K/yr
Reviews all batch documentation for accuracy and completeness according to cGMP's to ensure timely release. * Ensures deviations are initiated for any batch record review related events Find ...
Manufacturing Batch Record Coordinator
$57K - $107K/yr
Reviews all batch documentation for accuracy and completeness according to cGMP's to ensure timely release. * Ensures deviations are initiated for any batch record review related events Find ...
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 ...
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 ...
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 ...
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 ...
Review completed batch records, routers, inspection records, equipment logs, and supporting documentation for completeness, legibility, accuracy, required signatures, dates, and compliance with ...
New
Review completed batch records, routers, inspection records, equipment logs, and supporting documentation for completeness, legibility, accuracy, required signatures, dates, and compliance with ...
New
Support Quality Assurance (QA) Batch Record Review, Product Disposition, and QA Supplier Management including associated quality record management for small molecule, biologics, and device products
Support Quality Assurance (QA) Batch Record Review, Product Disposition, and QA Supplier Management including associated quality record management for small molecule, biologics, and device products
Support Quality Assurance (QA) Batch Record Review, Product Disposition, and QA Supplier Management including associated quality record management for small molecule, biologics, and device products
Support Quality Assurance (QA) Batch Record Review, Product Disposition, and QA Supplier Management including associated quality record management for small molecule, biologics, and device products
Are you resilient? The Master Batch Record (MBR) Designer will be presented with hard work ... Subject to motor vehicle report review. * Maintain valid driver's license and endorsements as ...
Are you resilient? The Master Batch Record (MBR) Designer will be presented with hard work ... Subject to motor vehicle report review. * Maintain valid driver's license and endorsements as ...
Are you resilient? The Master Batch Record (MBR) Designer will be presented with hard work ... Subject to motor vehicle report review. * Maintain valid driver's license and endorsements as ...
Quick apply
Are you resilient? The Master Batch Record (MBR) Designer will be presented with hard work ... Subject to motor vehicle report review. * Maintain valid driver's license and endorsements as ...
Review and sign batch records and manufacturing documents/ procedures as needed * Supports Operations, Quality Control, Quality Assurance and Program Management teams by providing expertise and ...
Review and sign batch records and manufacturing documents/ procedures as needed * Supports Operations, Quality Control, Quality Assurance and Program Management teams by providing expertise and ...
Review and sign batch records and manufacturing documents/ procedures as needed * Supports Operations, Quality Control, Quality Assurance and Program Management teams by providing expertise and ...
Review and sign batch records and manufacturing documents/ procedures as needed * Supports Operations, Quality Control, Quality Assurance and Program Management teams by providing expertise and ...
Review and sign batch records and manufacturing documents/ procedures as needed Supports Operations, Quality Control, Quality Assurance and Program Management teams by providing expertise and ...
Review and sign batch records and manufacturing documents/ procedures as needed Supports Operations, Quality Control, Quality Assurance and Program Management teams by providing expertise and ...
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 ...
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 ...
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 ...
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 ...
Biotech Batch Records Production Clerk
Santa Ana, CA · On-site
$19.65 - $24/hr
... etc. · While reviewing the batch record, tracks types of errors by the technicians, and works closely with Production management and technicians to eliminate reoccurrences. · Update material ...
Quick apply
Biotech Batch Records Production Clerk
Santa Ana, CA · On-site
$19.65 - $24/hr
... etc. · While reviewing the batch record, tracks types of errors by the technicians, and works closely with Production management and technicians to eliminate reoccurrences. · Update material ...
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.
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.
Batch Record Reviewer information
See salary details
$12.98 - $14.86
1% of jobs
$14.86 - $16.74
15% of jobs
$17.31 is the 25th percentile. Wages below this are outliers.
$16.74 - $18.62
31% of jobs
The median wage is $18.86 / hr.
$18.62 - $20.50
28% of jobs
$20.54 is the 75th percentile. Wages above this are outliers.
$20.50 - $22.38
12% of jobs
$22.38 - $24.26
8% of jobs
$24.26 - $26.14
4% of jobs
$26.14 - $28.02
1% of jobs
$28.02 - $29.90
0% of jobs
$29.90 - $31.77
0% of jobs
$31.77 - $33.65
0% of jobs
$12
$20
$33
How much do batch record reviewer jobs pay per hour?
What is a batch record reviewer?
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 batch record reviewer do?
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 skills and qualifications are needed to be a batch record reviewer?
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.
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Cities with the most Batch Record Reviewer job openings:
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States with the most job openings for Batch Record Reviewer jobs include:
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Night Shift QA Batch Record Reviewer/ Person in Plant, 4553936
San Carlos, CA • On-site
Contractor
Re-posted 25 days ago
Job 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.
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.
BS degree in science is preferred.
For more information, please contact
Akriti Gupta
(973) 967-3409
Morristown, NJ 07960
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