ExecutiveJobs Opening in Cadila Pharmaceuticals Ltd at Ankleshwar
FEATURED JOBExecutive
Cadila Pharmaceuticals Ltd
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Posted: 17 Dec 25
Job Description
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.
Job Particulars
Education Any Graduate
Who can apply Freshers
Hiring Process Face to Face Interview
Employment TypeFull Time
Job Id2809656
Job Category Manufacturing
Locality Address
State
Country India
About Company
Cadila Pharmaceuticals Ltd
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