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Quality Assurance Specialist Jobs
Company | Aavis Pharmaceuticals |
Address | , Hoschton, Ga |
Employment type | |
Salary | |
Expires | 2023-06-08 |
Posted at | 1 year ago |
(Hoschton, GA)
Develop and implement drug manufacturing safety guidelines and monitor product quality to ensure compliance standard and specifications with cGMP/GLP, ANDA, and 21CFR; Provide QA support for solid dosage; Review and ensure compliance of test results; Review Master Batch Records/Executed Batch Records, Change Controls; Review and approve technical documents (Process Validation, Equipment & Facility Validation), IPQA, CAPAs, SOPs, deviations, OOS, Handling of DEA documents, Provide support for all regulatory audits, internal/external inspections, and other audits.
Must have a Master’s Degree in Chemistry, Regulatory Affairs, or Pharmaceutical Science plus 1 year experience in job offered or as Formulation Associate. Require skills and knowledge in cGMP, Process Validation, batch records, SOPs, Deviations CAPAs, Change controls.
Job location: Hoschton, GA. Submit résumé referencing job code SOP001 to HR [email protected], Aavis Pharmaceuticals, 9488 Jackson Trail Road, Hoschton, GA 30548.
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