QA TECH
About The Position
Essential Job Responsibilities Product Sampling and Testing Submit samples to testing labs on a daily basis for finished goods and validation studies. Perform in-process tests as required and attach proper approval stickers to tanks and drums. Support receiving and verification of incoming raw materials and components. 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.
Requirements
- 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
Responsibilities
- Submit samples to testing labs on a daily basis for finished goods and validation studies.
- Perform in-process tests as required and attach proper approval stickers to tanks and drums.
- Support receiving and verification of incoming raw materials and components.
- 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.
Benefits
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
No Education Listed
