Greetings!!!
We are currently hiring for Facility Management professionals who have hands on experience in Working in Autoclave, Steam Sterilizer etc for our Leading Biopharmaceutical Company in Asia.
Designation: Executive to Senior Executive
Experience: 1 to 6 Years
Education: B.Tech
Job Description for Facility Management:
1. Operation of autoclave (steam steriliser), dry heat steriliser, ovens.
2. Maintenance of clean rooms by ensuring implementation of appropriate disinfection procedures.
3. Material preparation for sterilisation to meet process requirements which includes ensuring cleaning and sterilisation of process requirements.
4. Handling of Out of specifications, change controls, risk assessments and deviations related to area classification, sterilisation and WFI.
5. Qualification of sterilisers and cleanrooms.
6. Validation of cleaning procedures.
7. Monitoring area parameters such as temperature, DP and
8. Facility/Safety compliance, facility management, management of contract employee,
9. Plan, organize, execute, record, monitor and control area cleaning and disinfection program with adherence to SOP.
10. Sterilization of materials for process and routine requirements and operation of related equipment.
11. Reporting of non-conformities and deviations from SOPs.
12. Adherence to cGMP practices and follow laid down SOPs.
13. Plan, organize, execute, record, monitor and control process accessories cleaning program with adherence to SOP.
14. Monitoring of area parameters viz. temperature, differential pressure etc. through BMS and reporting non conformities.
15. Adherence to good microbiological practices.
16. Coordination with Engineering and Maintenance for preventive maintenance and calibration programs.
17. Preparation and review of documents, handling of change control, Issuing production documents
18. Equipment qualification and related documentation.
19. Preparation and review of protocols and reports related to qualification and validation. Execution of protocols and online reporting execution details.
20. Deviation investigation and CAPA implementation.
Interested please drop your profile to siva@bvrpc.com
1. Operation of autoclave (steam steriliser), dry heat steriliser, ovens.
2. Maintenance of clean rooms by ensuring implementation of appropriate disinfection procedures.
3. Material preparation for sterilisation to meet process requirements which includes ensuring cleaning and sterilisation of process requirements.
4. Handling of Out of specifications, change controls, risk assessments and deviations related to area classification, sterilisation and WFI.
5. Qualification of sterilisers and cleanrooms.
6. Validation of cleaning procedures.
7. Monitoring area parameters such as temperature, DP and
8. Facility/Safety compliance, facility management, management of contract employee,
9. Plan, organize, execute, record, monitor and control area cleaning and disinfection program with adherence to SOP.
10. Sterilization of materials for process and routine requirements and operation of related equipment.
11. Reporting of non-conformities and deviations from SOPs.
12. Adherence to cGMP practices and follow laid down SOPs.
13. Plan, organize, execute, record, monitor and control process accessories cleaning program with adherence to SOP.
14. Monitoring of area parameters viz. temperature, differential pressure etc. through BMS and reporting non conformities.
15. Adherence to good microbiological practices.
16. Coordination with Engineering and Maintenance for preventive maintenance and calibration programs.
17. Preparation and review of documents, handling of change control, Issuing production documents
18. Equipment qualification and related documentation.
19. Preparation and review of protocols and reports related to qualification and validation. Execution of protocols and online reporting execution details.
20. Deviation investigation and CAPA implementation.
Interested please drop your profile to siva@bvrpc.com
Thanks,
Sivaperuman.D.S
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