QA Technician

Eagle Labs, Inc; Tampa (FL); On-site; USD 36,000 - 48,000; Full time

Job summary

Eagle Labs, Inc in Tampa, FL seeks a Quality Assurance Full Time Clerical to support sampling, inspection, and documentation in a cGMP environment. This role protects product quality and regulatory compliance across production records.

Responsibilities include daily sampling of finished goods, preproduction inspections, batch record reviews, validation protocol readiness, and QA training. Strong Excel and Word skills are required.

Qualifications

• Must have two years’ experience in Quality Assurance or production, preferably in pharmaceutical or dietary supplements.
• Great attendance is required.
• Working knowledge of spreadsheet and word processing software such as Excel and Word.

Responsibilities

• Submit samples on a daily basis for finished goods and validation studies.
• Inspect production areas before production starts on a product.
• Inspect equipment before production starts and sign the cleaning log books.
• Inspect labels of products in production for correct label, expiration date and lot number as compared to the Batch Production Record.
• Inspect finished goods in the shipping area for correct QC Status (e.g. Quality Hold)
• Review test results and place with the Batch Production Record and Validation Protocol as required.
• Review Batch Production Records in production for completeness.
• Review Validation Protocols so that they are ready when production starts.
• Audit Batch Production Records to assure they are complete before giving to the QA Supervisor.
• Conduct training as needed for validation protocols.
• Understand, review, and participate in cGMP training.

Skills

Quality Assurance experience

Attendance

Tools

Excel

Word

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Quality Assurance Full Time Clerical Tampa, FL, US

2 days ago Requisition ID: 1186

Job Description

Product Sampling and Testing

• Submit samples on a daily basis for finished goods and validation studies.

Inspections

• Inspect production areas before production starts on a product.
• Inspect equipment before production starts and sign the cleaning log books.
• Inspect labels of products in production for correct label, expiration date and lot number as compared to the Batch Production Record.
• Inspect finished goods in the shipping area for correct QC Status (e.g. Quality Hold)

Review

• Review test results and place with the Batch Production Record and Validation Protocol as required.
• Review Batch Production Records in production for completeness.
• Review Validation Protocols so that they are ready when production starts.

Auditing

• Audit Batch Production Records to assure they are complete before giving to the QA Supervisor.

Training

• Conduct training as needed for validation protocols.
• Understand, review, and participate in cGMP training.

Job Qualifications

• Must have great attendance.
• Two years’ experience in Quality Assurance or production preferably in the pharmaceutical and/or dietary supplements industry
• Working knowledge of spreadsheet and word processing software such as Excel and Word