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| Job Location | Vishakhapatnam |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Pharma / Biotech |
| Functional Area | Operations Management / Process Analysis |
| EmploymentType | Full-time |
Description: Responsible for QMS related activities i. e. management of Documents and data control, Audit compliance, Risk Assessment, Change control, Deviations, Investigation, Market complaints, Product Recall, Preparation and maintenance of Internal audit schedules, Vendor Management, VMP. Preparation and review of documents required as per QA Project assigned for cGMP compliance and coordination with other department e. g. Qualification, Product validation, Cleaning validation , Training management of employee. Review of dispatches, analytical documents, validation execution qualification execution. Experience Required: 7 - 9 YearsLocation: VizagDepartment: Quality AssuranceUnit: IVSalary: At par within industry,
Keyskills :
risk training vendor qms cgmp qa control iskassessment vendormanagement trainingmanagement productvalidation auditcompliance cleaningvalidation marketcomplaints datacontrol internalaudit changecontrol