Cadila Pharma

Documentation:

•	To prepare SOP’s/ URS/ BPR/ Protocol/ Investigation report for regulatory compliance as per available procedure/practice.
•	Ensure that all documents / records required for Regulatory Compliance are maintained properly. 
•	Ensure old records are archived properly and are retrievable.
•	To check online filling of document & online submission to QA department.
•	Raise change control/ Deviation/ CAPA in OASIS LIMS.
•	To support SAP transaction in production module as & when required.
•	Raise indents for Consumables, parts, Stationary and Spares required for the plant.  
•	To ensure for high standards of housekeeping in plants.
•	To maintain all records and documents as per GDP/SOPs.
•	To take lead in audit preparedness and report to factory manager in case of any deviation.
•	To maintain training records of employees in respect of training SOP.
Production :
•	To perform the role of production officer/executive as and when required.
Cross Functional Department:
•	To coordinate with QA, department for compliance.
•	To coordinate with QC, PD Lab, Engineering and HR etc. for GMP Compliance.
•	To coordinate with EHS for safety and environment related audits.

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Skills Required

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