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QC Technician II
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$18 - $24 an hour
Full-time
- Perform visual and software inspection of all label proofs and associated documents, translation, and regulatory documentation (Translation work orders, order reports, excel results, client text and protocols), and randomizations, link reports, sample configurations, finished goods and replacement label requests.
- Correct documentation by noting and forwarding deficiencies to be corrected, tracking correction of deficiencies and verify corrections prior to approval.
- Communicate with the group leader, Project Managers and Project Support Associates during processing, and follow job completion.
- Ensure all relevant Standard Operating Procedures (SOPs), Work Instructions (WIs), master forms and Customer protocols are being followed in accordance with current Good Manufacturing Practices and company SOPs and WIs. This includes ensuring all current procedures and processes are being followed within the department.
- 2+ years' experience in a quality/ FDA cGMP environment
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