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Batch Record Review Jobs in Virginia (NOW HIRING)

Total Plastic Solutions

Quality Engineer

Lynchburg, VA · On-site

$70K - $90K/yr

Complete batch record review if required * Complete GSD and WMJ and review with Quality Manager * Attend weekly QE meetings * Medical QE will conduct process validation * Be a resource for the ...

Total Plastic Solutions

Quality Engineer

Lynchburg, VA · On-site

$65 - $95/hr

Complete batch record review if required; complete GSD and WMJ and review with Quality Manager. * Meetings and Validation: Attend weekly QE meetings; Medical QE will conduct process validation.

Orion Talent

Pharmaceutical Operator

Charlottesville, VA · On-site

$25/hr

Maintain proper documentation (batch records, production logs, etc.) * Write and review master documents as applicable: SOPs and batch records * Write Operation Deviation Reports * Supervise contract ...

Zimmer, Inc.

Document Control Coordinator

Norfolk, VA · On-site

How You'll Create Impact Responsible for review of batch records, creating Certificate of Conformances for product release, assisting with document control and records management processes, and for ...

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Batch Record Review information

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How much do batch record review jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for batch record review in Virginia is $20.16, according to ZipRecruiter salary data. Most workers in this role earn between $17.16 and $20.96 per hour, depending on experience, location, and employer.

What is a batch record reviewer?

A Batch Record Reviewer is a quality assurance professional responsible for reviewing and verifying production batch records in pharmaceutical or manufacturing environments. Their main role is to ensure that all documentation related to the production of each batch complies with regulatory standards and company procedures. This includes checking for accuracy, completeness, and compliance with Good Manufacturing Practices (GMP). By doing so, they help maintain product quality and safety before products are released to the market.

What skills and qualifications are needed to be a batch record reviewer?

To thrive as a Batch Record Reviewer, you need strong attention to detail, knowledge of Good Manufacturing Practices (GMP), and experience in pharmaceutical or biotechnology documentation, often supported by a degree in life sciences or related fields. Familiarity with electronic document management systems (EDMS), quality management software, and regulatory compliance tools is typically required. Excellent analytical skills, organization, and effective communication are standout soft skills for this role. These abilities ensure the accuracy, compliance, and completeness of batch records, which are critical for product quality and regulatory approval.

What are common challenges faced in a batch record review role, and how can they be addressed?

One common challenge in a Batch Record Review role is ensuring the completeness and accuracy of documentation while working under tight deadlines, as production schedules often depend on timely batch release. Attention to detail is critical, since even minor discrepancies can lead to delays or compliance issues. Effective communication and collaboration with production, quality assurance, and laboratory teams are key to resolving discrepancies quickly. Proactively staying updated on current Good Manufacturing Practices (cGMP) and internal protocols can also help minimize errors and streamline the review process.

What is the difference between Batch Record Review vs Quality Control Analyst?

AspectBatch Record ReviewQuality Control Analyst
Primary RoleReview and approve manufacturing batch records for compliance and accuracyPerform testing and analysis of raw materials, in-process, and finished products
CertificationsOften requires GMP, cGMP, or industry-specific certificationsRequires laboratory certifications, such as ASQ or equivalent
Work EnvironmentManufacturing or production facilities, quality assurance departmentsLaboratories, quality control labs, manufacturing sites
Industry UsagePharmaceutical, biotech, and manufacturing sectorsPharmaceutical, biotech, and food industries

While both roles focus on quality, Batch Record Review primarily involves reviewing manufacturing documentation for compliance, whereas Quality Control Analysts conduct testing and analysis to ensure product quality. Both are essential in regulated industries and often collaborate to maintain product standards.

What are the most commonly searched types of Batch Record Review jobs in Virginia?

The most popular types of Batch Record Review jobs in Virginia are:

What are popular job titles related to Batch Record Review jobs in Virginia?

For Batch Record Review jobs in Virginia, the most frequently searched job titles are:

What job categories do people searching Batch Record Review jobs in Virginia look for?

The top searched job categories for Batch Record Review jobs in Virginia are:

Batch Record Review jobs near you
Infographic showing various Batch Record Review job openings in Virginia as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, and 3% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $41,941 per year, or $20.2 per hour.

QA Associate - Pharmaceutical Manufacturing

Manassas, VA • On-site

Granules
See more jobs at Granulesexternal

Full-time

Re-posted 14 days ago

Job description

Description:

Granules Consumer Health, LLC is located in Manassas, Virginia. We have over 106 employees and annual revenue of $76.64 million. We serve as Granules’ packaging facility and front-end division for private label over the counter (OTC) products in the US.  We offer OTC generics that meet the highest level of quality at an affordable cost.  As such, we are well-established on bulk supply through efficiencies garnered through manufacturing, integration and a high level of regulatory compliance.  We are dedicated to excellence in manufacturing, quality, and customer service.  


The QA associate for documentation ensures compliance with cGMP and internal policies, procedures, and specifications. This position is responsible for performing inspections, batch record review, and quality system functions in accordance with cGMP and related company SOP’s, state, federal and local laws as applicable. This person should be knowledgeable of cGMP requirements, FDA regulations and ICH guidelines.


Job Duties & Responsibilities


  • Manage and maintain company document control and archival systems (hardcopy and electronic) in compliance with internal procedures and policies as well as regulatory requirements.
  • Manage the routing, review, approval, distribution and archival of new and revised controlled documents.
  • Track controlled documents through the issuance of Document Control numbers, logbooks, change requests, and document status reports.
  • Archive and maintain hardcopy and electronic copies of batch records files, audit files, vendor files, product, label files and change history files.
  • Control and issuance of labeling components.
  • Manage all document control logbooks and spreadsheets.
  • Perform the release of finished product batches packaged.
  • Provide new hire training on GMP’s, Safety, and Pharmacovigilance and maintain the training program documentation.
  • Ensure standard operating procedures are periodically reviewed for relevance and accuracy in compliance with company policies and procedures.
  • Collaborate with team members to ensure timely deliverables for documentation.
  • Ensuring all documents are up to date with respect to version control and issuance
  • Perform and support maintenance and closure activities of documents such as reports, protocols exceptions/deviations, CAPAs, change controls and complaints.
  • cGMP Compliance in Document Control.
  • Any other activity as assigned by the Supervisor


Requirements:


Knowledge & Skills


  • cGMP compliance within the pharmaceutical manufacturing industry.
  • Writing and maintaining cGMP documentation.
  • Analyze data/information and resolve complex issues.
  • Verbal and written communication skills.
  • Work and communicate with cross-functional teams.
  • Multiple priorities and re-prioritize tasks.


Experience & Education


  • At least two (2) years’ experience in a quality assurance role in a cGMP-regulated environment.
  • A college Degree preferably in Sciences (i.e. Pharmacy, Biology, Chemistry etc.)


Physical Requirements/Working Environment


  • While performing the duties of this job, the employee is regularly required to, stand, sit, talk, hear, and use hands and fingers to operate a computer and telephone keyboard.
  • Specific vision abilities required by this job include close vision requirements due to computer work.
  • Ability to sit at a computer terminal for an extended period of time.
  • Light to moderate lifting up to 10-15 lbs. is required.
  • Ability to work in a confined area.


We believe in fair and transparent pay practices. Actual compensation is determined based on relevant experience, qualifications, skills, and internal equity.