Pharma QA Technician: Testing, Inspections & Training

Automatic Data Processing, Inc.; Tampa (FL); On-site; USD 45,000 - 75,000; Full time

Job summary

Automatic Data Processing, Inc. in Tampa, FL is seeking a Quality Assurance Full Time Clerical position focused on QA sampling, inspections, and batch review to ensure compliance with cGMP standards.

The role includes submitting samples for finished goods and validation studies, inspecting production areas and equipment, reviewing test results and batch records, auditing Batch Production Records, and providing training on validation protocols and cGMP practices.

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

Responsibilities

• Submit samples daily for finished goods and validation studies.
• Inspect production areas before production starts and 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

Excellent attendance

Tools

Excel

Word

Job description

Automatic Data Processing, Inc. in Tampa, FL is seeking a Quality Assurance Full Time Clerical position focused on QA sampling, inspections, and batch review to ensure compliance with cGMP standards.

The role includes submitting samples for finished goods and validation studies, inspecting production areas and equipment, reviewing test results and batch records, auditing Batch Production Records, and providing training on validation protocols and cGMP practices.