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Weekend Qa Batch Record Review Jobs (NOW HIRING)

INCOG BioPharma Services

QA Associate

Fishers, IN · On-site

Support other QA personnel with batch record reviews, material release, etc. * Prioritize and ... This position will support primarily first shift (7 am to 4 pm) with occasional weekend support ...

PCI Pharma Services

Qa Specialist Ii - Ops

Bedford, NH · On-site

Primary responsibilities for this role includes Batch Record Review, Lot Disposition, and Quality ... This position may require additional hours and/or weekend work. #LI-RS1 Join us and be part of ...

PCI Pharma Services

Qa Specialist Ii - Ops

Bedford, NH · On-site

Primary responsibilities for this role includes Batch Record Review, Lot Disposition, and Quality ... This position may require additional hours and/or weekend work. #LI-RS1 Join us and be part of ...

Eisai

QA Specialist (Hybrid)

Raleigh, NC · On-site

$66K - $86K/yr

This role contributes to batch record review, documentation management, investigation support, and ... The QA Specialist, EMQO works collaboratively with internal stakeholders and business partners ...

Eisai

QA Specialist (Hybrid)

Raleigh, NC · Hybrid

$66K - $86K/yr

This role contributes to batch record review, documentation management, investigation support, and ... The QA Specialist, EMQO works collaboratively with internal stakeholders and business partners ...

kindeva

Senior Quality Assurance Specialist

Brentwood, MO · On-site

$77K - $106K/yr

Review and approve SOPs, Forms, Logbooks, and Master Batch Records for accuracy and regulatory ... Must be willing to work weekends and holidays as needed to support business initiatives * Lead ...

AbbVie

Analyst, QA

North Chicago, IL · On-site

$65K/yr

The QA Analyst supports the Quality Manager in the execution and oversight of the Quality System ... Reviews batch release documentation and batch records to support product disposition and shipment ...

AbbVie

Analyst, QA

North Chicago, IL

The QA Analyst supports the Quality Manager in the execution and oversight of the Quality System ... Reviews batch release documentation and batch records to support product disposition and shipment ...

New

Melaleuca, Inc.

QA Supervisor

Idaho Falls, ID · On-site

The Quality Assurance Supervisor plays a critical leadership role in protecting the integrity of ... The supervisor leads batch record review, CAPA and nonconformance management, document control ...

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Weekend Qa Batch Record Review information

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How much do weekend qa batch record review jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for weekend qa batch record review in the United States is $29.29, according to ZipRecruiter salary data. Most workers in this role earn between $18.75 and $34.38 per hour, depending on experience, location, and employer.
What are the most commonly searched types of Qa Batch Record Review jobs? The most popular types of Qa Batch Record Review jobs are:
Weekend Qa Batch Record Review jobs near you
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.

Quality Assurance Tech II

Endo International

Saint Louis, MO • On-site

Full-time

Re-posted 24 days ago

Job description

Why Us?
At Par Health, we believe great healthcare is built on getting the essentials right. We're looking for passionate, talented individuals who share our commitment to improving lives. With 4,000+ team members worldwide, we lead with pride and purpose-prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. Elevating the Essentials isn't just our tagline, it's the higher standard we live by every day.
Job Description Summary
The Quality Assurance Technician II performs a variety of review processes with the intent to correct record errors in manufacturing process documentation that includes batch record review and documentation issue resolution. This role is also responsible for return good inspections, cGMP area inspections and product inspections. This role ensures QA compliance and that cGMP principles are adhered to.
Job Description
ESSENTIAL FUNCTIONS:
  • Execute batch record review and document deficiencies in a computerized system
  • Identify exceptions and report exceptions to production
  • Resolve documentation discrepancies and issues with manufacturing operations personnel in a timely manner to allow for material release
  • Perform batch record accountability and Iron Mountain box reconciliation
  • Execute line clearances and assist in inspection of returned goods
  • Follow all internal and basic cGMP guidelines for pharmaceutical operations
  • Perform GMP walkthroughs with production on a routine basis
  • Participate in cross-functional teams to improve review efficiency and support
  • Adhere to all safety rules and maintain 100% completion of all safety required training
  • Maintain 100% on time Compliance Wire training

MINIMUM REQUIREMENTS:
Education:
HS Diploma is required; Associates or Bachelor's degree is preferred.
Experience:
  • Minimum of 1-3 years of document review experience in a cGMP environment preferred.
  • Proficiency in MS Word and Excel.
  • Proven knowledge of FDA and cGMP regulations preferred.
  • LIMS, BPCS, and TrackWise experience preferred.

Preferred Skills/Qualifications:
  • Ability to communicate at a high level of written and oral skills
  • Ability to read and comprehend complex calculations and formulas
  • Ability to focus and review batch records for an extended period of time
  • Knowledge of cGMPs for APIs
  • Ability to quickly identify, communicate and/or resolve issues
  • Ability to read and understand complex batch records
  • Ability to keep batch records organized and easily retrievable at all times
  • Excellent verbal and written communication skills
  • Ability to understand and apply good documentation practices
  • Ability to build relationships with partners

COMPETENCIES:
Organizing, Peer Relationships, Functional/Technical Skill, Time Management, Priority Setting, Attention to Detail
ORGANIZATIONAL RELATIONSHIP/SCOPE:
Reports to Quality Supervisor. Works with Manufacturing and Quality personnel on a daily basis
WORKING CONDITIONS:
  • 85 % Office environment which includes sitting for long periods of time and computer use.
  • 15 % Manufacturing environment exposure including temperature, noise, or chemical exposure.

DISCLAIMER:
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills require
EEO Statement:
We comply with all applicable federal, state, and local laws prohibiting discrimination and harassment, and provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status, or genetic information, or any other classification protected by federal, state or local law. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

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