ZipRecruiter

Log In

1

Weekend Qa Batch Record Review Jobs (NOW HIRING)

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 ...

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 ...

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 ...

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 ...

kindeva

Senior Quality Assurance Specialist

Brentwood, MO

$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 · On-site

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 ...

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 ...

INCOG

QA Associate, 2nd Shift

Fishers, IN

Support other QA personnel with batch record reviews, material release, etc. * Prioritize and ... This position will support primarily second shift (3 pm to 11:30 pm) with occasional weekend ...

INCOG

QA Associate, 2nd Shift

Fishers, IN · On-site

Support other QA personnel with batch record reviews, material release, etc. * Prioritize and ... This position will support primarily second shift (3 pm to 11:30 pm) with occasional weekend ...

previous page

Showing results 41-60

All JobsQa Batch Record Review JobsWeekend Qa Batch Record Review Jobs

Weekend Qa Batch Record Review information

See salary details

$12

$29

$62

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

As of Aug 6, 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.

QA Operations Specialist - Biopharmaceutical Manufacturing

SOKOL GxP Services

Devens, MA • On-site

$50 - $57.80/hr

Contractor

Medical, Retirement

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

We are seeking a QA Operations Specialist to support Quality Assurance activities within a biopharmaceutical manufacturing environment at the LSCC site in Devens, MA. This role provides on-the-floor QA support to manufacturing operations, ensuring compliance with company policies, procedures, and global cGMP requirements.
The QA Operations Specialist performs real-time batch record review, reviews manufacturing shop floor documentation, and supports quality decision-making in a regulated GMP environment. The role requires independent judgment, strong documentation skills, and the ability to partner effectively with manufacturing and cross-functional teams.
This is an intermediate-level role requiring 4-7 years of relevant experience.
Work Schedule
This position follows a rotating two-week schedule with 12.5-hour shifts (5:00 AM - 5:30 PM):
Week 1
• Work: Tuesday, Wednesday
• Off: Thursday, Friday
• Work: Saturday, Sunday, Monday
Week 2
• Off: Tuesday, Wednesday
• Work: Thursday, Friday
• Off: Saturday, Sunday, Monday
The two-week rotation repeats continuously.
Holidays are worked as business needs require.
Key Responsibilities:
  • Provide on-the-floor QA support to manufacturing operations;
  • Ensure compliance with approved procedures and batch records;
  • Perform real-time review of manufacturing batch records;
  • Review and approve shop-floor manufacturing documentation;
  • Identify, assess, and escalate quality issues as appropriate;
  • Support deviation investigations, change controls, and CAPA activities;
  • Apply Quality Risk Management principles in daily decision-making;
  • Partner cross-functionally to support continuous improvement initiatives;
  • Develop and revise GMP procedures as required.

Requirements
Must Haves:
  • Required manufacturing shop floor documentation experience.
  • Strong authorship skills with the ability to critically review investigations, interpret results, and generate technical conclusions consistent with Quality Risk Management principles.

Required Qualifications:
  • Associate's or Bachelor's degree in a relevant discipline.
  • Minimum 4 years of relevant Quality Assurance experience in an FDA-regulated cGMP environment.
  • Strong knowledge of US and global cGMP requirements.
  • Experience supporting GMP manufacturing and/or warehousing operations.
  • Working knowledge of quality processes including deviations, investigations, change control, material disposition, product complaints, and CAPA management.
  • Ability to work independently with moderate direction on complex tasks.
  • Confidence in making decisions for non-routine quality issues.
  • Strong written and verbal communication skills.
  • Strong organizational skills with the ability to multitask in a fast-paced manufacturing environment.

Benefits
Competitive hourly rate: $50 - $57.8/hr (W-2 only, no C2C)
12-month contract with possible extension
Health insurance, holiday pay, 401(k) program, and other benefits
Employee referral bonus program

Apply