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 ...
Manager, QA Batch Disposition
Harmans, MD · On-site
Manager, QA Batch Disposition Position Summary: * Work Schedule: Monday - Friday, 8am - 5pm. * 100 ... Monitor and oversee real-time batch record review activities, escalating issues as needed to ...
Manager, QA Batch Disposition
Harmans, MD · On-site
Manager, QA Batch Disposition Position Summary: * Work Schedule: Monday - Friday, 8am - 5pm. * 100 ... Monitor and oversee real-time batch record review activities, escalating issues as needed to ...
Senior QA Batch Disposition Specialist
Fishers, IN · On-site
$77K - $106K/yr
Lead full lifecycle review and disposition of parenteral manufacturing batch records (Formulation ... Manage QA Hold status and serve as the primary QA point of contact for client-facing disposition ...
Senior QA Batch Disposition Specialist
Fishers, IN · On-site
$77K - $106K/yr
Lead full lifecycle review and disposition of parenteral manufacturing batch records (Formulation ... Manage QA Hold status and serve as the primary QA point of contact for client-facing disposition ...
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 ...
Provide Client access and support in the review and approval of Batch Records. Provide training to all QA Associates and Specialists on surveillance oversight and on-the-floor Batch Record review ...
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Provide Client access and support in the review and approval of Batch Records. Provide training to all QA Associates and Specialists on surveillance oversight and on-the-floor Batch Record review ...
QA Batch Review Specialist
Fishers, IN · On-site
Provide Client access and support in the review and approval of Batch Records. Provide training to all QA Associates and Specialists on surveillance oversight and on-the-floor Batch Record review ...
QA Batch Review Specialist
Fishers, IN · On-site
Provide Client access and support in the review and approval of Batch Records. Provide training to all QA Associates and Specialists on surveillance oversight and on-the-floor Batch Record review ...
QA Batch Review Specialist
Fishers, IN · On-site
Provide Client access and support in the review and approval of Batch Records. Provide training to all QA Associates and Specialists on surveillance oversight and on-the-floor Batch Record review ...
QA Batch Review Specialist
Fishers, IN · On-site
Provide Client access and support in the review and approval of Batch Records. Provide training to all QA Associates and Specialists on surveillance oversight and on-the-floor Batch Record review ...
Discover Impactful Work The Quality Assurance Specialist III - Batch Release plays a critical role ... A Day in the Life • Perform comprehensive batch record review to support product release in ...
Discover Impactful Work The Quality Assurance Specialist III - Batch Release plays a critical role ... A Day in the Life • Perform comprehensive batch record review to support product release in ...
Discover Impactful Work The Quality Assurance Specialist III - Batch Release plays a critical role ... A Day in the Life • Perform comprehensive batch record review to support product release in ...
Discover Impactful Work The Quality Assurance Specialist III - Batch Release plays a critical role ... A Day in the Life • Perform comprehensive batch record review to support product release in ...
Documentation Specialist I
Fremont, CA · 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 · 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 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 ...
Senior Specialist, Field Quality QA Operations
Devens, MA · On-site
$91K - $126K/yr
The Senior Field QA Specialist is responsible for reviewing Manufacturing Batch Records (MBRs), performing real time on-the-floor exceptions reviews and logbooks, conducting GMP area walkthroughs ...
Senior Specialist, Field Quality QA Operations
Devens, MA · On-site
$91K - $126K/yr
The Senior Field QA Specialist is responsible for reviewing Manufacturing Batch Records (MBRs), performing real time on-the-floor exceptions reviews and logbooks, conducting GMP area walkthroughs ...
Senior Specialist, Field Quality QA Operations
$91K - $126K/yr
The Senior Field QA Specialist is responsible for reviewing Manufacturing Batch Records (MBRs), performing real time on-the-floor exceptions reviews and logbooks, conducting GMP area walkthroughs ...
Senior Specialist, Field Quality QA Operations
$91K - $126K/yr
The Senior Field QA Specialist is responsible for reviewing Manufacturing Batch Records (MBRs), performing real time on-the-floor exceptions reviews and logbooks, conducting GMP area walkthroughs ...
Quality Assurance Associate
Columbia, SC · On-site
$26.60/hr
The Quality Assurance Associate II is responsible for maintaining all training of a QAA I in ... Batch record review for completeness, accuracy, and compliance to TRC standards * Verification of ...
Quality Assurance Associate
Columbia, SC · On-site
$26.60/hr
The Quality Assurance Associate II is responsible for maintaining all training of a QAA I in ... Batch record review for completeness, accuracy, and compliance to TRC standards * Verification of ...
The Quality Assurance Associate II is responsible for maintaining all training of a QAA I in ... Batch record review for completeness, accuracy, and compliance to TRC standards * Verification of ...
The Quality Assurance Associate II is responsible for maintaining all training of a QAA I in ... Batch record review for completeness, accuracy, and compliance to TRC standards * Verification of ...
QA Specialist IV
Lexington, MA · 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 · 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 · On-site
$120 - $165/hr
Position Summary The Manager QA- MQA supports documentation control, batch record review, sampling activities, material releases, investigations, and manufacturing quality oversight. This role ...
New
Quality Assurance Manager
Chandler, AZ · On-site
$120 - $165/hr
Position Summary The Manager QA- MQA supports documentation control, batch record review, sampling activities, material releases, investigations, and manufacturing quality oversight. This role ...
New
QA Specialist
San Diego, CA · 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 · 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.
Quality Assurance Manager
$27 - $32/hr
In addition to batch record review and documentation control, the QA Specialist will contribute to deviation writing, investigation reporting, and continuous improvement initiatives. The ideal ...
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Quality Assurance Manager
$27 - $32/hr
In addition to batch record review and documentation control, the QA Specialist will contribute to deviation writing, investigation reporting, and continuous improvement initiatives. The ideal ...
Quality Assurance Technician
Carlisle, PA · 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 · 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 ...
Freelance Qa Batch Record Review information
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Night Shift QA Batch Record Reviewer/ Person in Plant, 4553936
San Carlos, CA • On-site
Contractor
Re-posted 23 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