Biologics represent the cutting-edge of biomedical research, and biosimilars present an enormous opportunity to provide affordable access to these advanced therapies. Biosimilars are intended to increase patients’ access to biologics as they are priced lower than branded, novel biologics and may further lead to the competitive pricing of the original biologic.
Job Description: Greeting from Biocon Biologics Limited !!!
Important Details :
1) Ensure & Implementation of Data Integrity Culture in Quality Control Lab.
2) Adherence to cGMP (Current Good Manufacturing Practice), cGLP (Current Good Laboratory Practice) and GDP (Good Documentation Practice).
3) Qualification of Analytical instruments and Equipment (IQ/OQ/PQ) and Facility readiness.
4) Receipt of in process, DS, reserve samples and stability samples and storage at QC location.
5) Planning and performing In-Process, finished product (DS) and stability sample testing of Monoclonal antibodies and reporting the results. Enter batch result in SAP.
6) Preparation of stability protocol, registration and inventory in Nova LIMS.
7) Review of analytical reports of In process, finished product, stability, method validation, method transfer and study, Review of usage log books and Observation data sheets.
8) Preparation and review of method validation, method transfer, study protocol, Stability protocols and summary sheet (Compilation Data) and reports.
9) Planning and performing (Testing) of method transfer, method validation and study samples.
10) Verification of laboratory compliances, which include the validity checking of the reagents, standards, system status etc.
11) Reporting and investigation of Incidents, OOS, OOT and Deviation.
12) Supporting Operational Excellence, 5S in Quality control Lab.
13) Calibration of analytical weighing balance, HPLC, UV, IR, and pH meter etc.
14) Monitoring of EMS and reviewing the reports.
15) Review of ICDAS .
16) Maintenance of stability chamber, daily alarm log acknowledgement, temperature data verification.
1) Ensure & Implementation of Data Integrity Culture in Quality Control Lab.
2) Adherence to cGMP (Current Good Manufacturing Practice), cGLP (Current Good Laboratory Practice) and GDP (Good Documentation Practice).
3) Qualification of Analytical instruments and Equipment (IQ/OQ/PQ) and Facility readiness.
4) Receipt of in process, DS, reserve samples and stability samples and storage at QC location.
5) Planning and performing In-Process, finished product (DS) and stability sample testing of Monoclonal antibodies and reporting the results. Enter batch result in SAP.
6) Preparation of stability protocol, registration and inventory in Nova LIMS.
7) Review of analytical reports of In process, finished product, stability, method validation, method transfer and study, Review of usage log books and Observation data sheets.
8) Preparation and review of method validation, method transfer, study protocol, Stability protocols and summary sheet (Compilation Data) and reports.
9) Planning and performing (Testing) of method transfer, method validation and study samples.
10) Verification of laboratory compliances, which include the validity checking of the reagents, standards, system status etc.
11) Reporting and investigation of Incidents, OOS, OOT and Deviation.
12) Supporting Operational Excellence, 5S in Quality control Lab.
13) Calibration of analytical weighing balance, HPLC, UV, IR, and pH meter etc.
14) Monitoring of EMS and reviewing the reports.
15) Review of ICDAS .
16) Maintenance of stability chamber, daily alarm log acknowledgement, temperature data verification.
Required Education Qualification: Msc
Required Experience: 1 – 6 years
𝗖𝗮𝗿𝗲𝗲𝗿 𝗢𝗽𝗽𝗼𝗿𝘁𝘂𝗻𝗶𝘁𝘆 𝗮𝘁 𝗦𝘂𝗻𝗿𝗶𝘀𝗲 𝗥𝗲𝗺𝗲𝗱𝗶𝗲𝘀 𝗣𝘃𝘁. 𝗟𝘁𝗱.🚀 We are expanding our team and looking for…
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