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Deputy Manager

Cadila Pharmaceuticals

Full-timeOn-siteregulatory compliancesop documentationurs documentationbpr documentationprotocol documentationinvestigation report preparationdocument managementchange controldeviation managementcapa managementoasis limssapproduction managementaudit preparednesstraining record maintenancegmp complianceehs audit coordinationstakeholder management

Location:Ankleshwar, IndiaType:Full-timePosted:Today

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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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