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Executive

Cadila Pharmaceuticals Limited

0 years

|

0 Lacs

Dholka Gujarat India

Posted:3 days ago| Platform:

Apply

Skills Required

processing documentation manufacturing risk assessment monitoring audit qc maintenance training mentoring calibration

Work Mode

On-site

Job Type

Full Time

Job Description

Working on Unit operations related to downstream processing during Drug Substance (DS) manufacturing.
GMP documentation related to DS manufacturing like batch records, equipment usage, facility monitoring.
Preparation of documents like SOPs, MMDS and QMS related documents like change control, deviation, CAPA, risk assessment etc.
Monitoring of manufacturing facility and keep it cGMP compliant
Involvement during regulatory audit preparation
Co-ordination with cross functional teams like QC, QA, Maintenance, Warehouse, Injection etc.
Training and mentoring new joinees
Keep the track for calibration and qualification activities, for example for equipment, weighing scale and standards etc

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Cadila Pharmaceuticals Limited

Pharmaceuticals

Ahmedabad

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