2.0 - 7.0 years

3 - 8 Lacs

Palasbari

Work from Office

1. To maintain and ensure cGMP/cGLP in the Quality Control Department. 2. To maintain documents as per GLP requirements. 3. To perform the activity as per work allotment. 4. To follow the SOP/ATP/STP and protocols. 5. To maintain the laboratory neat and clean. 6. To perform sampling and analysis of Packing material sample and maintain online documentation. 7. To maintain the data integrity and to plan the work such as to give maximum productivity within stipulated time. 8. To perform daily monitoring of temperature. 9. To participate with supervisor to close the investigation for deviation, Incidents, OOT and OOS. 10. To follow safety procedure in the laboratory. 11. To report the result of analysis carried out by contract laboratory. 12. To perform all operation in QC lab carried out as per the written procedure. 13. Handling of LIMS software and LMS software etc. Secondary responsibility: 1. To perform analysis of Raw material,FP,PV/AMT sample and Stability Sample and maintain online documentation as and when required. 2. To perform the daily verification of instrument as and when required. 3. Any other additional work allocated by reporting authority. Interested candidates can send resumes to akash.gogoi@sunpharma.com Job Location: Palashbari, Mirza, Assam Contact No: 8473959757

Posted 19 hours ago

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Sterile/Parenteral Production Officer Sun Pharma

3.0 - 8.0 years

3 - 8 Lacs

Palasbari

Work from Office

1. He is authorized to sign (as a Doer/Checker) Parenteral GMP documents, Batch Manufacturing record Process validation Record Daily observation compliance Qualification document Execution of aseptic process simulation (Media Fill) Department SOPs (EDMS) and study protocol Assign to person in CAPA, Initiator and lead investigator in incident and investigation. 2. He can Perform and ensure the equipment cleaning and usage log, Start-up activities and line clearance, Documentation practices, labelling practices throughout operation. 3. Preparation or assist of various protocol and reports, as required in execution of process validation, cleaning validation/verification and characterization batches. 4. The supervisor is responsible for production activities of clean area day to day basis in achieving total production requirements in quality, quantity and GMP compliance in preparation area. 5. Preparation and reviewing of process related logbooks, SOP(s), BMR and other relevant documents. 6. Daily recording of RH, Temperature and differential pressure of area and equipment as per requirement. 7. Working as per instruction provided by Senior to achieve the daily production plan. 8. Co-ordination with engineering department for preventive maintenance schedule. 9. Participate relevant training prior to perform any activity. 10. To follow aseptic behaviour in side aseptic area. 11. Generate requirement for Consumable Items and other miscellaneous items (SAP) required for smooth production operation. 12. Responsible for maintenance and inventory control, safe keeping and availability of change over parts and spare part. 13. Involving in planning, execution as per planning and allocation/managing of manpower. 14. Responsible for Manufacturing area and all production related activity in parenteral department. 15. Handling of additional activities/task allotted by HOD. Interested candidates can send resumes to akash.gogoi@sunpharma.com Job Location: Palashbari, Mirza. Assam Contact No: 8473959757

Posted 19 hours ago

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