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| Job Location | Delhi |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Recruitment Services |
| Functional Area | General / Other Software |
| EmploymentType | Full-time |
DUTIES RESPONSIBILITIES- 1- He must have experience in Quality Control in medical devices manufacturing unit. 2-Preparation of SOPs, Formats and other QC related documents and timely revision. 3-Inspection testing of incoming raw material as per specifications and prepare inspection reports 4-Inspection testing of in-process material as per specifications and prepare inspection reports 5-Inspection testing of finished products as per specifications and prepare inspection reports 6-Verification and compilation of BPR 7-To plan all outsourced testing activities (sterility, EO residual, environmental monitoring, water testing etc.) and ensure all reports are received on time(certificate of analysis) 8-Assistance in validation and calibration of equipment like pH meter, weighing balance, sealing machine, water bath, hot plate, oven, Vernier calliper, pull-push meter, scale, etc. 9-Preparation of documents and records for various audits - Drug department, ISO, CE customer audits,
Keyskills :
calibrationquality control documentationglp chemical analysiscontinuous improvement facilitation ph meterms office