The QA & RA Supervisor will be liable for progression and effective rendering of the changeable quality control program to satisfy specifications of ISO 9001:2008, ISO 13485 quality control systems and FDA’s 21CFR, area 820 quality program control for Medical Equipment.
The selection should usually have experts in Total Good quality Administration and B.Sc in Technical Technological innovation and should be a lead auditor for ISO9001:2008/ISO 13485 quality control program. The individual must have a bare minimum practical knowledge of 5 years in program progression, rendering, and examine of ISO 9001:2008/ISO 13485 quality control program in a developing industry. The individual should also have good IT skills, be highly encouraged & result-oriented, and should have strong authority features.
The settlement program will be beautiful, based on degree practical knowledge and attached to key operation signs or symptoms (KPI) which will be motivated by the Board of Company directors.
Interested People should mail their application and records along with a recent image to the attention of time manager at P.O. Box 1094 Sialkot
The selection should usually have experts in Total Good quality Administration and B.Sc in Technical Technological innovation and should be a lead auditor for ISO9001:2008/ISO 13485 quality control program. The individual must have a bare minimum practical knowledge of 5 years in program progression, rendering, and examine of ISO 9001:2008/ISO 13485 quality control program in a developing industry. The individual should also have good IT skills, be highly encouraged & result-oriented, and should have strong authority features.
The settlement program will be beautiful, based on degree practical knowledge and attached to key operation signs or symptoms (KPI) which will be motivated by the Board of Company directors.
Interested People should mail their application and records along with a recent image to the attention of time manager at P.O. Box 1094 Sialkot
