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Quality Events Technical Writer
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- Piper Life Sciences is actively seeking a Quality Events Technical Writer to join a gene therapy organization developing innovative AAV platform products for challenging diseases.
- The Quality Assurance Specialist will be responsible for the review and approval of data in a GMP environment.
- This is a Monday - Friday, traditional hours role that is hybrid in Durham, North Carolina.
- Responsible for compliance review of pharmaceutical manufacturing data throughout the facility.
- Collaborate with cross functional groups like manufacturing, process development, and other departments liable for GMP activities, to support resolution of deviations and other compliance discrepancies.
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