Quality Control (QC) Executive
at SUNWARD PHARMACEUTICAL PRIVATE LIMITED
Singapore, Southeast, Singapore -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 15 Aug, 2024 | USD 4000 Monthly | 15 May, 2024 | N/A | Good communication skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
SUMMARY OF JOB SCOPE:
Responsible for technical enhancement of quality control and analytical development in QC Laboratory functions.
- Work allocation and arrangement for daily QC routine work
- Finish Product Quality Control
- Checking Report of “In-Process control of Tablet”
- In process quality control of intermediates (IPQC)
- Review and evaluation of Analyst test report and data to ensure test result is up-to date and accurate.
- Review and ensure QC Records and BMR are up-to-date, complete and accurate.
- Supervision of quality control check on raw material dispensing
- Management, Monitering and testing on sample.
- Monitor retained samples and waste of tested sample of intermediates and finished products.
- Environment monitoring and recording for retention sample room.
- Supervision and training of laboratory technicians and laboratory assistant and chemist in carrying out their duties.
- Responsibe to revise of SOP for IPQC and FPQC and relevant section.
- Verify and approve test result in absence of QC Manager.
- Calibration of laboratory equipment and apparatus.
- Ensure Good Laboratory Practice (GLP) & Lab Safety.
- Optimization of usage of laboratory equipment.
- Support in the investigation and management of product complaints.
- Participate in process and cleaning validation.
Responsibilities:
- Work allocation and arrangement for daily QC routine work
- Finish Product Quality Control
- Checking Report of “In-Process control of Tablet”
- In process quality control of intermediates (IPQC)
- Review and evaluation of Analyst test report and data to ensure test result is up-to date and accurate.
- Review and ensure QC Records and BMR are up-to-date, complete and accurate.
- Supervision of quality control check on raw material dispensing
- Management, Monitering and testing on sample.
- Monitor retained samples and waste of tested sample of intermediates and finished products.
- Environment monitoring and recording for retention sample room.
- Supervision and training of laboratory technicians and laboratory assistant and chemist in carrying out their duties.
- Responsibe to revise of SOP for IPQC and FPQC and relevant section.
- Verify and approve test result in absence of QC Manager.
- Calibration of laboratory equipment and apparatus.
- Ensure Good Laboratory Practice (GLP) & Lab Safety.
- Optimization of usage of laboratory equipment.
- Support in the investigation and management of product complaints.
- Participate in process and cleaning validation
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Singapore, Singapore