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Quality Assurance Data Annotation Jobs in Florida

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 ... data, deviations, and trend analysis. * Verified adherence to Good Manufacturing Practices (GMP ...

Quality Assurance * Technical & Report Writing * Business Communication * Content Review & Editing * Data Interpretation * Data Annotation * Fact Checking * Independent Research * Problem-Solving

SUMMARY: QA Lead of Data & Reporting is responsible for ensuring the quality and integrity of data and reporting processes within the organization, while also leading a team of QA professionals. This ...

SUMMARY: QA Lead of Data & Reporting is responsible for ensuring the quality and integrity of data and reporting processes within the organization, while also leading a team of QA professionals. This ...

Support data quality, monitoring, and drift detection practices. * Ensure compliance with ... Lead QA efforts across multiple Agile/Scrum teams. * Participate in PI planning, sprint ceremonies ...

Vistrue and ASG believe deeply in the power of people and data to grow great organizations, and ... To learn more, visit and Quality Assurance Analyst The Mission of the Role Vistrue is looking for a ...

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Quality Assurance Data Annotation information

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Infographic showing various Quality Assurance Data Annotation job openings in Florida as of August 2026, with employment types broken down into 84% Full Time, 8% Part Time, and 8% Contract. Highlights an 83% In-person, and 17% Remote job distribution.

Quality Assurance

GL Staffing Services, Inc.

Boca Raton, FL • On-site

$55K - $57K/yr

Full-time

Posted 21 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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