QA Technician

Eagle Labs, Inc; Largo (FL); On-site; USD 40,000 - 55,000; Full time

Job summary

Eagle Labs, Inc in Largo, FL is seeking a Quality Assurance Full Time Clerical candidate. The role focuses on sample submission, inspections, and reviews to support production and validation activities in a cGMP environment.

Responsibilities include auditing Batch Production Records, training on validation protocols, and ensuring QA compliance throughout the manufacturing process.

Qualifications

• 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.
• Must have great attendance.

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

Excel

Word

QA experience

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 Largo, FL, US

2 days ago Requisition ID: 1188

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