QA Batch Record Reviewer
Miami, FL · On-site
Disposition, review, and verify tissue sent for irradiation and sterilization. * Confirm the ... Some evening and weekend work may be required to ensure customer commitments and goals are met.
Miami, FL · On-site
Disposition, review, and verify tissue sent for irradiation and sterilization. * Confirm the ... Some evening and weekend work may be required to ensure customer commitments and goals are met.
Miami, FL · On-site
Disposition, review, and verify tissue sent for irradiation and sterilization. * Confirm the ... Some evening and weekend work may be required to ensure customer commitments and goals are met.
Miami, FL · On-site
Disposition, review, and verify tissue sent for irradiation and sterilization. * Confirm the ... Some evening and weekend work may be required to ensure customer commitments and goals are met.
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Miami, FL · On-site
Disposition, review, and verify tissue sent for irradiation and sterilization. * Confirm the ... Some evening and weekend work may be required to ensure customer commitments and goals are met.
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 ...
The Quality Assurance Batch Record Coordinator is responsible for coordinating, reviewing, tracking, maintaining, and archiving production and quality batch documentation to ensure records are ...
The Quality Assurance Batch Record Coordinator is responsible for coordinating, reviewing, tracking, maintaining, and archiving production and quality batch documentation to ensure records are ...
The Quality Assurance Batch Record Coordinator is responsible for coordinating, reviewing, tracking, maintaining, and archiving production and quality batch documentation to ensure records are ...
The Quality Assurance Batch Record Coordinator is responsible for coordinating, reviewing, tracking, maintaining, and archiving production and quality batch documentation to ensure records are ...
Fishers, IN · On-site
$74K - $102K/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 ...
Fishers, IN · On-site
$74K - $102K/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 ...
Fishers, IN · On-site
$90 - $140/hr
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 ...
Fishers, IN · On-site
$90 - $140/hr
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 ...
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 ...
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 ...
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 role requires a strong QA background with hands-on batch record review experience and GMP manufacturing environment experience. Key Responsibilities Batch Record Review & Product Disposition
New
The role requires a strong QA background with hands-on batch record review experience and GMP manufacturing environment experience. Key Responsibilities Batch Record Review & Product Disposition
New
Santa Monica, CA · On-site
$55K - $83K/yr
You will also be expected to independently coordinate and manage timelines for batch record reviews ... Flexibility of occasionally working in weekend or holidays to support lot release. * Ability to ...
New
Santa Monica, CA · On-site
$55K - $83K/yr
You will also be expected to independently coordinate and manage timelines for batch record reviews ... Flexibility of occasionally working in weekend or holidays to support lot release. * Ability to ...
New
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 ...
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 ...
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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 ...
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 ...
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 ...
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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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 ...
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 ...
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 ...
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 ...
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 ...
Reviews all SOPs, policies, work instructions, batch records, etc. regarding visual inspection, defects, rejects, and defect kits. * Develops QA documents for visual inspection AQL inspection.
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Reviews all SOPs, policies, work instructions, batch records, etc. regarding visual inspection, defects, rejects, and defect kits. * Develops QA documents for visual inspection AQL inspection.
Reviews all SOPs, policies, work instructions, batch records, etc. regarding visual inspection, defects, rejects, and defect kits. * Develops QA documents for visual inspection AQL inspection.
Reviews all SOPs, policies, work instructions, batch records, etc. regarding visual inspection, defects, rejects, and defect kits. * Develops QA documents for visual inspection AQL inspection.
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 ...
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 ...
$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
The most popular types of Qa Batch Record Review jobs are:

Description
Job Purpose
The Quality Assurance (QA) Batch Record Reviewer performs the Technical and Final release function of the graft release process. The QA Batch Record Reviewer performs functions necessary to assure that all relevant manufacturing records are assembled, reviewed, and completed in a compliant efficient manner, and ultimately determines and documents the final disposition of each graft on the controlled batch records and in the VIVEX Biologics computer system. This position requires attention to detail and must be performed in accordance with standard operating procedures, as well as all applicable state, regulatory and AATB requirements.
Duties and Responsibilities
2. Work closely with operations and customer service personnel on inventory needs for customer orders and back orders.
3. Knowledgeable of the VIVEX BTM computer system and able to perform all functions as required.
4. Responsible for reporting all variances, errors and deviations to Quality Assurance.
5. Able to collaborate on complaint and/or nonconformance reports according to VIVEX procedure.
6. Performs other duties as assigned by the Manager and Director of the Department.
Requirements
Qualifications
Working Conditions
Primarily a quiet office-oriented work environment. Some evening and weekend work may be required to ensure customer commitments and goals are met.
Physical Requirements
While performing the duties of this job, the employee is regularly required to sit for prolonged periods of time. The employee may occasionally be required to pull, lift and/or move up to 20 pounds.
Direct Reports
No direct reports.
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Biotechnology research and development
201 - 500 Employees
Miami, FL, US
2012