Experience spanning three decades in healthcare, with a wide range of formulations to meet the needs of ailing humanity, Intas Pharmaceuticals headquartered at Ahmedabad (India), is now a force to reckon with, in the global pharma horizon. With expertise in a range of formulations, from tablets to injectables to newer drug delivery systems, Intas is currently ranked 17th among the Indian Pharma majors. A variety of initiatives in Research and Development, patents and ANDA filing, NDDS, quality manufacturing support, along with approvals by regulatory authorities of many countries has made Intas a global healthcare provider.
Vacancy Details
Job description
1. Equipment/instrument Qualification activity
2. FAT, SAT, DQ, IQ, OQ, PQ
3. Must be monitored and verified documents i.e. calibrations certificates, MOC certificates, etc
4. New SOPs to be prepare if required at QA end.
5. Protocol & report be additional prepared if required at QA end.
6. Monitoring of updating in Site Master File if required.
7. Monitoring of preventing maintenance schedule, calibration schedule for gauges temp. sensor etc.
8. To checked and find out gap for operation, cleaning procedure of old and new equipment.
Share resume at recruitment_hr@intaspharma.com
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