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Work Mode

On-site

Job Type

Full Time

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.

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Cadila Pharmaceuticals Limited logo
Cadila Pharmaceuticals Limited

Pharmaceuticals

Ahmedabad

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