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Quality Assurance Engineer
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- Provide day-to-day Quality support of the warehouse, manufacturing, packaging, and batch record review areas.
- uthor, review, and approve cGMP documents, including various procedures, protocols, specifications, reports, records, and changes to these documents.
- Responsible for opening change controls and initiating, maintaining, and reviewing specific procedures relative to warehouse, manufacturing, and packaging.
- Interface with members of quality compliance and assurance team on quality related issues.
- 5+ years of work experience in Quality Assurance or Regulatory Affairs in a cGMP pharmaceutical and/or biological manufacturing regulated environment preferred.
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