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| Job Location | Chennai |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Pharma / Biotech |
| Functional Area | Operations Management / Process Analysis,Sales / BD |
| EmploymentType | Full-time |
Will be responsible for IPQA activity in Manufacturing and Packing.Responsible for the batch release section for review the BPR for proper compliance and fill the BRC with proper documents during batch release.To monitor the Quality Assurance Activities on Production floor w.r.t the manufacturing formulation and Packing i.e. Tablet.To ensure conformance of system and work practice with standard operating procedure based on good manufacturing practices.To certify Area/line clearance prior to commencement of manufacturing and packing activities for a batch as per cGMP guideline.On line review and compilation of BMR/BPR to ensure the proper recording the data.In process, QA checks on the formulation with information to concern section in charge for the corrective action, if any.Coordination with other department for smooth function.Required Candidate profile Must be willing to relocate to Chennai Should have exposure in USFDA Perks and Benefits ,
Keyskills :
miscustomer servicedocumentationfinanceinsurancestandard operating procedurecontinuous improvement facilitationbatch releasequality assurancecorrective actionbprbrcipqacgmpusfdacheckspackingbenefitsassurance