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Executive Qa Batch Record Review Jobs (NOW HIRING)

Quality Assurance

Boca Raton, FL · On-site

$55K - $57K/yr

In-Process Quality Assurance Specialist Time: 7am-7pm or 7pm-7am Salary: $55/ $69k Responsibilities ... Reviewed and prepared Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR) to ensure ...

Quality Assurance Specialist Location: Pomona, California Duration: 12 Months 100% Onsite Summary ... Perform batch record review, record administration, and batch release activities. * Review and ...

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 ...

... in batch record reviews to ensure documentation is complete, compliant, and ready for release. Support release activities by coordinating documentation readiness and collaborating with QA team ...

Quality Assurance Reporting To: QA Manager / QA Director Responsible For (Staff): No The QA ... Primary responsibilities for this role includes Batch Record Review, Lot Disposition, and Quality ...

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

As of Aug 22, 2026, the average hourly pay for executive qa batch record review in the United States is $23.19, according to ZipRecruiter salary data. Most workers in this role earn between $17.55 and $24.28 per hour, depending on experience, location, and employer.

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Quality Assurance

GL Staffing Services, Inc.

Boca Raton, FL • On-site

$55K - $57K/yr

Full-time

Posted 25 days ago


Job description

In-Process Quality Assurance Specialist

Time: 7am-7pm or 7pm-7am

Salary: $55/ $69k

Responsibilities:

  • Performed in-process quality assurance activities for sterile pharmaceutical manufacturing operations in accordance with cGMP guidelines and regulatory requirements from the U.S. Food and Drug Administration.
  • Conducted line clearance before and after manufacturing operations to ensure proper equipment status, material segregation, and compliance with approved procedures.
  • Performed in-process sampling of sterile products during manufacturing to verify product quality and compliance with approved specifications.
  • Reviewed and prepared Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR) to ensure completeness, accuracy, and adherence to standard operating procedures.
  • Participated in batch record review and batch release activities, ensuring all manufacturing and quality documentation met regulatory and internal quality standards.
  • Assisted in the review of Annual Product Quality Review (APQR) reports by compiling manufacturing data, deviations, and trend analysis.
  • Verified adherence to Good Manufacturing Practices (GMP) and supported quality compliance during production operations.
  • Investigated deviations, documented observations, and collaborated with production and quality teams to implement corrective actions.
  • Ensured manufacturing and documentation activities complied with quality standards such as those from the International Organization for Standardization and pharmaceutical regulatory guidelines.
  • Coordinated with Quality Control, Production, and Regulatory teams to maintain product quality and ensure successful batch release.

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