Pharmaceuticals located in San Carlos is seeking a Quality Assurance Batch Record Reviewer / Person ... Responsible for on-the-floor, timely and effective GMP review and production close-out of batch ...
Pharmaceuticals located in San Carlos is seeking a Quality Assurance Batch Record Reviewer / Person ... Responsible for on-the-floor, timely and effective GMP review and production close-out of batch ...
Experience performing end-of-process Quality Assurance activities; Quality Control experience alone is not sufficient. * Experience reviewing and scanning manufacturing batch records. * Working ...
Quick apply
Experience performing end-of-process Quality Assurance activities; Quality Control experience alone is not sufficient. * Experience reviewing and scanning manufacturing batch records. * Working ...
Sie fuhren die Ihnen zugewiesenen Tatigkeiten in SAP, Veeva und weiteren QA-Datenbanken durch und pflegen interne Nachverfolgungslisten fur Batch Record Reviews und regulatorische Einreichungen.
Sie fuhren die Ihnen zugewiesenen Tatigkeiten in SAP, Veeva und weiteren QA-Datenbanken durch und pflegen interne Nachverfolgungslisten fur Batch Record Reviews und regulatorische Einreichungen.
The Quality Program Management Supervisor will oversee and guide the QA batch record review and product disposition team. The supervisor is responsible for fostering strong client quality ...
The Quality Program Management Supervisor will oversee and guide the QA batch record review and product disposition team. The supervisor is responsible for fostering strong client quality ...
The Quality Program Management Supervisor will oversee and guide the QA batch record review and product disposition team. The supervisor is responsible for fostering strong client quality ...
The Quality Program Management Supervisor will oversee and guide the QA batch record review and product disposition team. The supervisor is responsible for fostering strong client quality ...
Quality Assurance Associate
Santa Monica, CA ยท On-site
$55K - $83K/yr
The successful candidate will contribute to the advancement of our product pipeline by performing QA batch record review, label review and verifications, document archival of records, and other ...
Quality Assurance Associate
Santa Monica, CA ยท On-site
$55K - $83K/yr
The successful candidate will contribute to the advancement of our product pipeline by performing QA batch record review, label review and verifications, document archival of records, and other ...
Documentation Specialist I
Fremont, CA ยท On-site
... QA batch disposition deadlines are met. * Independently executes (paper/electronic) batch record review * Collaborates within Manufacturing to resolve batch record discrepancies or errors as it ...
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Documentation Specialist I
Fremont, CA ยท On-site
... QA batch disposition deadlines are met. * Independently executes (paper/electronic) batch record review * Collaborates within Manufacturing to resolve batch record discrepancies or errors as it ...
QA Specialist
Costa Mesa, CA ยท On-site
$65K - $75K/yr
The QA Specialist is responsible for independently conducting thorough review of batch production ... Batch Record Review * Independently review executed batch records and associated documents (testing ...
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QA Specialist
Costa Mesa, CA ยท On-site
$65K - $75K/yr
The QA Specialist is responsible for independently conducting thorough review of batch production ... Batch Record Review * Independently review executed batch records and associated documents (testing ...
QA Batch Review and Product Release ... Review executed batch records for completeness, accuracy and compliance with approved procedures ...
QA Batch Review and Product Release ... Review executed batch records for completeness, accuracy and compliance with approved procedures ...
Facilitate an environment of teamwork and communication between Quality Assurance, Production and other support functions to ensure on-time Quality review of batch records in order to achieve ...
Facilitate an environment of teamwork and communication between Quality Assurance, Production and other support functions to ensure on-time Quality review of batch records in order to achieve ...
QA Associate
Corona, CA ยท On-site
$18 - $26/hr
Perform batch record GMP compliance review (21 CFR 211.192) at reviewer level; final approval is granted by the QA Manager * Support complaint investigations and coordinate complaint sample testing ...
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QA Associate
Corona, CA ยท On-site
$18 - $26/hr
Perform batch record GMP compliance review (21 CFR 211.192) at reviewer level; final approval is granted by the QA Manager * Support complaint investigations and coordinate complaint sample testing ...
Facilitate an environment of teamwork and communication between Quality Assurance, Production and other support functions to ensure on-time Quality review of batch records in order to achieve ...
Facilitate an environment of teamwork and communication between Quality Assurance, Production and other support functions to ensure on-time Quality review of batch records in order to achieve ...
QA Specialist IV
Lexington, MA ยท On-site
Conducting record review of executed batch records for finish drug products to support CMO ... the QA unit Supports drug product and finish drug product annual review report sections ...
QA Specialist IV
Lexington, MA ยท On-site
Conducting record review of executed batch records for finish drug products to support CMO ... the QA unit Supports drug product and finish drug product annual review report sections ...
Quality Assurance Manager
Chandler, AZ ยท On-site
Position Summary The Manager QA- MQA supports documentation control, batch record review, sampling activities, material releases, investigations, and manufacturing quality oversight. This role ...
Quality Assurance Manager
Chandler, AZ ยท On-site
Position Summary The Manager QA- MQA supports documentation control, batch record review, sampling activities, material releases, investigations, and manufacturing quality oversight. This role ...
Specialist QA-Drug Substance
Juncos, PR ยท On-site
Perform comprehensive Batch Record Review for completeness, accuracy, compliance, and adherence to procedures and GMP. * Review and approve product MPs. * Approve process validation protocols and ...
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Specialist QA-Drug Substance
Juncos, PR ยท On-site
Perform comprehensive Batch Record Review for completeness, accuracy, compliance, and adherence to procedures and GMP. * Review and approve product MPs. * Approve process validation protocols and ...
QA Specialist
San Diego, CA ยท On-site
$90K - $125K/yr
The QA Operations Specialist will support the Abzena operations teams to drive continuous ... Be an SME of batch record review and disposition of buffers / media manufactured by Abzena.
QA Specialist
San Diego, CA ยท On-site
$90K - $125K/yr
The QA Operations Specialist will support the Abzena operations teams to drive continuous ... Be an SME of batch record review and disposition of buffers / media manufactured by Abzena.
Discover Impactful Work As a Lead QA Technician, you will play a critical role in ensuring product ... quality systems * Strong expertise in batch record review, deviation management, CAPA, and root ...
Discover Impactful Work As a Lead QA Technician, you will play a critical role in ensuring product ... quality systems * Strong expertise in batch record review, deviation management, CAPA, and root ...
Discover Impactful Work As a Lead QA Technician, you will play a critical role in ensuring product ... quality systems * Strong expertise in batch record review, deviation management, CAPA, and root ...
Discover Impactful Work As a Lead QA Technician, you will play a critical role in ensuring product ... quality systems * Strong expertise in batch record review, deviation management, CAPA, and root ...
Quality Assurance Technician
Carlisle, PA ยท On-site
Our Client is looking for Quality Assurance Technician Summary: Accountable for activities involved ... Responsibilities: Support Manufacturing batch record review activities. Prepare and issue ...
Quality Assurance Technician
Carlisle, PA ยท On-site
Our Client is looking for Quality Assurance Technician Summary: Accountable for activities involved ... Responsibilities: Support Manufacturing batch record review activities. Prepare and issue ...
This role includes reviewing manufacturing batch records, cleaning batch records, analytical batch records, and other supporting documentation to support batch disposition. The QA Dispositioner ...
This role includes reviewing manufacturing batch records, cleaning batch records, analytical batch records, and other supporting documentation to support batch disposition. The QA Dispositioner ...
Qa Batch Record Review information
See salary details
$12.98 - $17.44
17% of jobs
$18.91 is the 25th percentile. Wages below this are outliers.
$17.44 - $21.90
24% of jobs
The median wage is $24.13 / hr.
$21.90 - $26.35
18% of jobs
$26.35 - $30.81
15% of jobs
$31.18 is the 75th percentile. Wages above this are outliers.
$30.81 - $35.27
10% of jobs
$35.27 - $39.73
8% of jobs
$39.73 - $44.19
5% of jobs
$44.19 - $48.65
3% of jobs
$48.65 - $53.10
0% of jobs
$53.10 - $57.56
0% of jobs
$57.56 - $62.02
0% of jobs
$12
$29
$62
How much do qa batch record review jobs pay per hour?
What is a QA Batch Record Review?
A QA Batch Record Review job involves reviewing manufacturing batch records to ensure compliance with company policies, regulatory requirements, and Good Manufacturing Practices (GMP). The role ensures that all documentation is accurate, complete, and meets quality standards before product release. Responsibilities may include identifying discrepancies, coordinating with production teams for corrections, and maintaining compliance with FDA or other regulatory guidelines. This position is essential in the pharmaceutical, biotechnology, and healthcare industries to ensure product safety and consistency.
What are the main responsibilities and challenges faced by someone in a QA Batch Record Review role?
A QA Batch Record Review professional is responsible for reviewing production and manufacturing records to ensure compliance with regulatory standards and identify any discrepancies or deviations. This role often requires meticulous attention to detail, as even small errors in documentation can impact product release or trigger audits. A key challenge is balancing thoroughness and efficiency under demanding production schedules. Typically, individuals in this role collaborate closely with production, quality assurance, and regulatory teams to resolve issues and maintain a smooth workflow. This position can offer career growth into broader quality assurance or compliance roles within the pharmaceutical or manufacturing industry.
What are the key skills and qualifications needed to thrive in the QA Batch Record Review position, and why are they important?
To thrive as a QA Batch Record Review specialist, you typically need a background in life sciences or a related field along with strong attention to detail and knowledge of Good Manufacturing Practices (GMP). Familiarity with electronic batch record systems, regulatory documentation, and quality control or assurance certifications are often required. Excellent analytical skills, effective communication, and the ability to work both independently and collaboratively are valuable soft skills in this position. These skills ensure that all production records are accurate, compliant, and meet quality standards, which is critical for maintaining product integrity in regulated industries.
What cities are hiring for Qa Batch Record Review jobs?
Cities with the most 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:
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States with the most job openings for Qa Batch Record Review jobs include:
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For Qa Batch Record Review jobs, the most frequently searched job titles are:

Night Shift QA Batch Record Reviewer/ Person in Plant, 4553936
San Carlos, CA โข On-site
Contractor
Re-posted 18 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.ย
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: ย
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 07960ย
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