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Qa Batch Record Review Jobs (NOW HIRING)

Lonza

QA Specialist II-Lot review

Portsmouth, NH · On-site

QA Specialist II - Lot Review Location: This position is based in our Portsmouth, NH office. The ... Perform detailed review of manufacturing batch records and supporting documentation for ...

Lonza

QA Specialist II-Lot review

Portsmouth, NH

QA Specialist II - Lot Review Location: This position is based in our Portsmouth, NH office. The ... Perform detailed review of manufacturing batch records and supporting documentation for ...

Alan Baird Industries

Batch Record Reviewer

Allendale, NJ · On-site

$19 - $22/hr

Review batch records and travelers for completeness, accuracy, and compliance. * Release product in accordance with internal procedures and quality standards. * Ensure all documentation adheres to ...

Actalent

QA Associate

Clinton, IN

Experience with batch record review and batch record maintenance. * Knowledge of cGMP principles and quality assurance practices. * Ability to perform QA tests, QA checks, and QA documentation tasks ...

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

As of Aug 7, 2026, the average hourly pay for 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 key skills and qualifications needed to thrive in the QA Batch Record Review position, and why are they important?

To thrive as a QA Batch Record Review specialist, you typically need a background in life sciences or a related field along with strong attention to detail and knowledge of Good Manufacturing Practices (GMP). Familiarity with electronic batch record systems, regulatory documentation, and quality control or assurance certifications are often required. Excellent analytical skills, effective communication, and the ability to work both independently and collaboratively are valuable soft skills in this position. These skills ensure that all production records are accurate, compliant, and meet quality standards, which is critical for maintaining product integrity in regulated industries.

What is a QA Batch Record Review?

A QA Batch Record Review job involves reviewing manufacturing batch records to ensure compliance with company policies, regulatory requirements, and Good Manufacturing Practices (GMP). The role ensures that all documentation is accurate, complete, and meets quality standards before product release. Responsibilities may include identifying discrepancies, coordinating with production teams for corrections, and maintaining compliance with FDA or other regulatory guidelines. This position is essential in the pharmaceutical, biotechnology, and healthcare industries to ensure product safety and consistency.

What are the main responsibilities and challenges faced by someone in a QA Batch Record Review role?

A QA Batch Record Review professional is responsible for reviewing production and manufacturing records to ensure compliance with regulatory standards and identify any discrepancies or deviations. This role often requires meticulous attention to detail, as even small errors in documentation can impact product release or trigger audits. A key challenge is balancing thoroughness and efficiency under demanding production schedules. Typically, individuals in this role collaborate closely with production, quality assurance, and regulatory teams to resolve issues and maintain a smooth workflow. This position can offer career growth into broader quality assurance or compliance roles within the pharmaceutical or manufacturing industry.

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Qa Batch Record Review jobs near you
Infographic showing various 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 Manager

Diversified Sourcing Solutions

Birmingham, AL

$27 - $32/hr

Full-time

Posted 24 days ago

Job description

Diversified Sourcing Solutions is seeking a highly detailoriented QA Specialist to support Quality Assurance activities within a regulated pharmaceutical manufacturing environment. This role plays a critical part in ensuring documentation accuracy, GMP compliance, and timely resolution of quality issues. In addition to batch record review and documentation control, the QA Specialist will contribute to deviation writing, investigation reporting, and continuous improvement initiatives. The ideal candidate thrives in a structured environment, enjoys problemsolving, and is motivated by maintaining the highest standards of product quality and patient safety.

Key Responsibilities
  • Issue, track, and maintain controlled documents in accordance with document control procedures
  • Scan, file, and organize quality and production documentation to ensure full traceability
  • Support data entry and maintenance of quality trending logs and quality system metrics
  • Perform detailed, realtime review of batch records for accuracy, completeness, and GMP compliance
  • Continuously review production logs and documentation for proper entries and adherence to procedures
  • Provide floor support to Operations to ensure batch records are completed correctly and consistently
  • Work within ISO Class 8 cleanroom environments following proper gowning procedures
  • Follow all safety procedures when working in controlled environments involving hazardous drug products
  • Identify documentation discrepancies and escalate issues promptly to the Quality team
  • Draft and support deviation reports, including initial documentation, rootcause identification, and corrective/preventive action tracking
  • Assist with investigation reporting to ensure timely closure and compliance with internal and regulatory expectations
  • Maintain organized, compliant, and auditready documentation practices at all times
Qualifications
  • Experience in Quality Assurance, documentation review, deviation writing, or GMP compliance within pharmaceutical, biotechnology, or other regulated manufacturing environments preferred
  • Familiarity with GMP documentation practices, batch record review, and quality systems
  • Strong attention to detail, accuracy, and organizational skills
  • Ability to manage and review documentation efficiently in a fastpaced production environment
  • Comfortable working in cleanroom environments and following gowning procedures
Compensation
  • $27.00 – $32.00 per hour, depending on experience

Schedule:
  • 1st Shift, 8:30 AM – 5:00 PM

Diversified Sourcing Solutions provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, or genetics.

Company Description

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