Quality Control (QC) Executive

at  SUNWARD PHARMACEUTICAL PRIVATE LIMITED

Singapore, Southeast, Singapore -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate15 Aug, 2024USD 4000 Monthly15 May, 2024N/AGood communication skillsNoNo
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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