QA Technician

Engramec; Largo (FL); On-site; USD 42,000 - 65,000; Full time

Job summary

Engramec is seeking a Quality Assurance professional in Largo, FL to support daily sampling of finished goods and validation studies. The role involves inspecting production areas, equipment, and labels to ensure compliance with batch records.

The candidate reviews test results, batch production records, and validation protocols, and participates in cGMP training. Strong attendance and experience in pharma or dietary supplements are preferred.

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 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

cGMP knowledge

Excel

Word

Attendance

Tools

Excel

Word

Job description

• 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