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 workplace related audits.

📌 Assistant Manager (Ankleshwar)
🏢 Cadila Pharmaceuticals
📍 Ankleshwar