QA Technician

ACGME

Largo, FLFull time
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Location
Largo, FL
Job type
Full time
Posted
Oct 26
4 days ago
Career path

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About the company

ACGME

Hospital & health care · 201 to 500 employees

ACGME on LinkedIn

What you'll do

  • Submit samples daily for finished goods and validation studies
  • Inspect production areas and equipment before production starts
  • Inspect product labels and finished goods in the shipping area
  • Review test results, Batch Production Records and Validation Protocols
  • Audit Batch Production Records before giving them to the QA Supervisor
  • Conduct training as needed for validation protocols
  • Understand, review, and participate in cGMP training

What you need

  • 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

Key skills

Quality AssuranceExcelWordcGMP

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Perks

  • Dental insurance
  • Health insurance
  • Paid time off
  • Vision insurance

See full description on company page, apply now

Read the full posting here
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 Job Type: Full-time Monday through Thursday. Benefits: Dental insurance Health insurance Paid time off Vision insurance Monday through Friday Various shifts

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