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Weekend Qa Batch Record Review Jobs (NOW HIRING)

AbbVie

PR · On-site

The batch record review encompasses manufactured batch records, investigation of deviations ... Availability to work second and third shifts, including weekends and holidays. Additional ...

INCOG

QA Batch Specialist

Fishers, IN · On-site

The QA Specialist - Batch Review will at all times provide support with identifying and closing ... Full lifecycle review and disposition of parenteral manufacturing Batch Records (Formulation ...

Actalent

Quality Assurance Specialist

Norwood, MA

$42 - $52/hr

Review and approve batch production records, testing records, and manufacturing documentation ... Skills Quality assurance, drug substance, drug product, Batch record, raw materials, deviations ...

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Infographic showing various Weekend 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 $60,925 per year, or $29.3 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

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