ZipRecruiter

Log In

2

Remote Batch Record Review Jobs (NOW HIRING)

Managed Staffing

HEDIS Reviewer

MI · Remote

$44 - $45/hr

Remote - Must reside in Michigan (MI) Schedule: Monday - Friday, 8:00 AM - 5:00 PM Job Summary: HEDIS Reviewer III (Medical Record Review Abstractor) to support HEDIS quality reporting. This role ...

Agilent

Operational Excellence Lead: BioVectra

Boston, MA · On-site +1

... batch-record review, deviation handling, and client response, then install the daily management and standard work that level the work and shorten time to release. • Partner with Quality to support ...

next page

Showing results 1-20

All JobsBatch Record Review JobsRemote Batch Record Review Jobs

Remote Batch Record Review information

See salary details

$12

$20

$33

How much do remote batch record review jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for remote batch record review in the United States is $20.34, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $21.15 per hour, depending on experience, location, and employer.

What is a remote batch record review?

A Remote Batch Record Review job involves reviewing manufacturing batch records for accuracy, completeness, and compliance with regulatory and company standards. This role ensures that all documentation meets Good Manufacturing Practices (GMP) and other quality requirements before product release. The position is typically performed remotely, requiring strong attention to detail, knowledge of regulatory guidelines, and experience in quality assurance or manufacturing documentation.

What are the typical daily responsibilities of someone in a remote batch record review role?

Daily responsibilities usually include reviewing manufacturing batch records for completeness, accuracy, and compliance with regulatory standards, as well as identifying and documenting discrepancies. You may be required to collaborate remotely with production, quality, and regulatory teams to resolve issues and clarify record details. Maintaining up-to-date documentation and ensuring timely submission of records are key tasks. This role often involves working independently with strict deadlines, but also relies on clear communication and teamwork to ensure quality and compliance throughout the manufacturing process.

What are the key skills and qualifications needed to thrive in the remote batch record review position, and why are they important?

To thrive as a Remote Batch Record Review professional, you need a solid understanding of Good Manufacturing Practices (GMP), quality assurance principles, and experience with batch record documentation, often supported by a degree in science or a related field. Familiarity with electronic document management systems (EDMS), quality management software, and regulatory databases is typically required. Strong attention to detail, organizational skills, and clear written communication are essential soft skills for this role. These abilities ensure accuracy, compliance, and efficiency in reviewing records critical to pharmaceutical or manufacturing operations.

More about Remote Batch Record Review jobs
What cities are hiring for Remote Batch Record Review jobs? Cities with the most Remote Batch Record Review job openings:
What states have the most Remote Batch Record Review jobs? States with the most job openings for Remote Batch Record Review jobs include:
What job categories do people searching Remote Batch Record Review jobs look for? The top searched job categories for Remote Batch Record Review jobs are:
Remote Batch Record Review jobs near you
Infographic showing various Remote Batch Record Review job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 6% Part Time, and 6% Contract. Highlights an 100% Remote job distribution, with an average salary of $42,304 per year, or $20.3 per hour.

Master Batch Record (MBR) Designer - 1099/W2

GMP Pros, Inc.

Omaha, NE • Remote

Other

Re-posted 6 days ago

Job description

Are you a GMP Pro?!

  • Are you a proactive doer?
  • Do you need variety and change to keep from getting bored?
  • Do you build relationships easily and are you able to communicate information so that it is easily understandable?
  • Do you like working in a team supportive environment where others want to help you succeed?
  • Do you try to find a better way for everything because that is the way it should be?
  • Do you thrive in organized chaos and high-pressure situations?
  • Do you quickly become an expert in any subject matter you are working in?
  • Can you stay motivated and help motivate others in the face of adversity and change? Are you resilient?



The Master Batch Record (MBR) Designer will be presented with hard work, relentless challenges, and the pressure of high expectations. The MBR Designer is responsible for developing, configuring, and maintaining electronic Master Batch Records within a manufacturing execution system (MES) to support compliant and efficient production.


Be part of an exciting start-up that supports the world’s leading pharmaceutical, biotech, food, and animal health companies. Get the best of both worlds. Gain experience at a company that leads projects for global pharmaceutical companies while enjoying the flexibility, energy, and personal attention that can only be found working in a small, close-knit company. 


APPLICANTS MUST HAVE PRIOR EXPERIENCE IN BIOTECH, PHARMACEUTICAL, OR ANIMAL HEALTH INDUSTRIES TO BE CONSIDERED


Essential Duties: 

  • Work with a project team to understand business requirements for design and deployment of PAS-X across manufacturing and packaging for Oral Solids Dosage.
  • Take design blueprints and translate into GMBRs, MBRs, PMBRs, PVLs, and ESPs for the deployment.
  • Support the creation and management of Master Data.
  • Support integration of hardware and infrastructure (printers, scanners, clients).
  • Test and troubleshoot designs with end users in the DEV environment.
  • Support verification and validation of designs in the PROD environment.
  • Support Early Life Support and Hyper Care for deployment activities across the site.
  • Maintain project deliverables and milestone dates.


Requirements: 

  • Bachelor’s degree in Life Sciences, Pharmaceutical Sciences, Industrial, Chemical, Mechanical, or Automation Engineering, or a related technical field.
  • MES platform-based training or certification (e.g. Koerber PAS-X Training) preferred
  • 3 - 5 years of experience in pharmaceutical manufacturing, quality assurance, or technical writing with exposure to batch record development.
  • Minimum of 2 - 3 years of hands-on design experience with electronic batch record (eBR) systems such as PAS-X, Pharmasuite, Siemens opCenter, etc. (PAS-X preferred).
  • Proven experience mapping business processes (e.g. Visio or Lucid Chart)
  • Knowledge of GMP, FDA 21 CFR Part 11, and other relevant regulatory standards.
  • Practical experience working in a project environment with a project team.


Some other things that you will need to be successful:

  • Experienced in an FDA-regulated environment.
  • Excellent communication and organization skills, with an analytical and problem-solving mindset.
  • Ability to multi-task and complete multiple projects on time.

Pre-Employment Requirements: 

  • Pass and maintain pre-employment/contract background check and safety certification, including but not limited to outstanding professional references.
  • Subject to motor vehicle report review.
  • Maintain valid driver’s license and endorsements as required per position.
  • Pass pre-employment/contract physical, medical evaluation, and drug screen due to the safety sensitive nature of this position.
  • Successfully complete and maintain any required safety certification and testing on an annual basis.


Work Environment Expectations 

  • This role can be remote with occasional on-site work
GMP Pros logo

About GMP Pros

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

11 - 50 Employees

Headquarters location

Omaha, NE, US

Year founded

2013

View All GMP Pros Jobs