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Quality Assurance Specialist (Biotechnology)
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- A Pharmaceutical client is looking for a Senior Quality Assurance Specialist , specifically with documentation experience in biotechnology or pharmaceutical industry
- Senior QA Documentation Specialist, you will be instrumental in the management and evolution of the Veeva Learning Management System to meet the challenges of compliance in late-stage clinical drug product and commercial drug product.
- The Senior QA Documentation Specialist will be responsible for supporting the daily activities of Documentation Management.
- Maintaining the Record Retention Schedule for GxP documents/records
- Filing/Archiving GxP documents/records as required
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