Deputy Manager
Cadila Pharmaceuticals Ltd
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Posted: 03 Sep 26
Job Description
JOB RESPONSIBILITIES
1. Working on Unit operations related toupstream processing during Drug Substance (DS)
manufacturing.
2. GMP documentation related to DS manufacturing like batch records, equipment usage, facility
monitoring.
3. Preparation of documents like SOPs, MMDs and QMS related documents like change control, deviation, CAPA, risk assessment etc.
4. Monitoring of manufacturing facility and keep it cGMP compliant
5. Involvement during regulatory audit preparation
6. Co-ordination with cross functional teams like QC, QA, Maintenance, Warehouse, Injection etc.
7. Training and mentoring new joinees
8. Keep the track for calibration and qualification activities, for example for equipment, weighing scale and standards etc.
9. Preparation and maintenance of virus stocks and cell banks
Job Particulars
Role research jrf srf
Education Any Graduate
Who can apply Freshers
Hiring Process Face to Face Interview
Employment TypeFull Time
Job Id2951417
Job Category Research
Locality Address
State Gujarat
Country India
About Company
Cadila Pharmaceuticals Ltd
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