Experience

OLIVE HEALTHCARE LIMITED

• United Kingdom
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Senior Officer

  • Mar 2023 - Present



Intas Pharmaceuticals

• India
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Senior Officer

  • Sep 2021 - Feb 2023



Exemed Pharamceuticals

• India
• Consumer Services
• 1 - 100 Employee

• Quality Assurance Officer

  • Jul 2020 - Aug 2021

  Responsible for ensuring cGMP & GMP compliances at shop floor as per respective SOP. Line clearance activities in manufacturing stages. Responsible for in process check during manufacturing stages. Knowledge on production online monitoring activities etc. To check cleaning of all area and personal hygiene. Good equipment handling. To perform all IPQA activities. To collect the sample from manufacturing stages & hold time study sample as per BMR and protocol instructions. To ensure online compliance of BMR and BPR entries. Humidity record, online check test data sheet log book entries. Monthly Audit trail of UV-Spectrophotometer, IR, Karl Fischer, Auto-Titrator. Preparation of APQR. Issuance of Specification, Logbooks and Control. Control Sample (FP) Maintenance and Documentation. Daily quality control dept round and warehouse store department round Responsible for ensuring GLP compliances at QC Lab as per respective SOP. Review of API Material COA. Review of Raw Material COA. Review the Stability Report. Investigation of incident and OOS result Review of Finished Product COA. Review of Packing Material COA. Review of EM Trend. eview of all instrument log book online. Monthly Review of all instrument log book. Document tracking Show less



SUN PHARMA

• Pharmaceutical Manufacturing
• 700 & Above Employee

• Apprentice

  • Jul 2018 - Jul 2019

  Control Sample (FP) Maintenance and Documentation. ➢ Log Book issuance and control. ➢ Log Book retrieval and tracking. ➢ Preparation of APQR. ➢ Issuance of Specification and Control. ➢ Preparation of standard operating procedures (SOP’s). Control Sample (FP) Maintenance and Documentation. ➢ Log Book issuance and control. ➢ Log Book retrieval and tracking. ➢ Preparation of APQR. ➢ Issuance of Specification and Control. ➢ Preparation of standard operating procedures (SOP’s).