- Keeps up-to-date on regulations/ development of biopharmaceutical QC method/ technology to ensure the project maximizes the use of digitalization, automation and robotics.
8 days
31 QC Jobs in Malaysia | Job Vacancies | October 2026 | Ricebowl
Showing 31 jobs results for
"qc"
- Keeps up-to-date on regulations/ development of biopharmaceutical QC method/ technology to ensure the project maximizes the use of digitalization, automation and robotics.
2 days
- Keeps up-to-date on regulations/ development of biopharmaceutical QC method/ technology to ensure the project maximizes the use of digitalization, automation and robotics.
4 days
- Learn analytical methods and in-house reagents used in QC Laboratory
2 days
- Operate, calibrate and perform basic troubleshooting for laboratory equipment; arrange maintenance with vendors as required.
30+ days
- Learn analytical methods and in-house reagents used in QC Laboratory
3 days
- Identifies and reports problems in QC. Solve problems and implement corrective actions.
8 days
- Identifies and reports problems in QC. Solve problems and implement corrective actions.
9 days
- Manage material / supplier qualification in compliance with cGMP requirement and internal procedures.
24 days
- We are committed to creating an inclusive workplace and providing equal opportunities for all applicants. We embrace an agile working culture across our roles, so if flexibility is important to you please discuss opportunities with our hiring team. If you need any adjustments to the recruitment process to help you demonstrate your strengths and capabilities, contact [email protected] . Please note this email is for adjustment requests only; for other enquiries please use our standard contact channels.
24 days
- Act as QA approver for deviations, CAPAs, change controls and SOPs, ensuring timely, compliant closure.
19 days
- Act as QA approver for deviations, CAPAs, change controls and SOPs, ensuring timely, compliant closure.
8 days
- Act as QA approver for deviations, CAPAs, change controls and SOPs, ensuring timely, compliant closure.
30+ days
- Act as QA approver for deviations, CAPAs, change controls and SOPs, ensuring timely, compliant closure.
30+ days
- Maintain various tracker, e.g. QI tracker, checklist review tracker, QTO tracker
Today
- Maintain various tracker, e.g. QI tracker, checklist review tracker, QTO tracker
1 day
- Perform analysis, if required, of QC operations testing for utilities, raw materials, manufacturing processes and products and ensure that the tests are analyzed in accordance with corporate, regulatory and external agency regulations
1 day
- Perform analysis, if required, of QC operations testing for utilities, raw materials, manufacturing processes and products and ensure that the tests are analyzed in accordance with corporate, regulatory and external agency regulations
2 days
- Lead or participate in investigation arising from micro related and utilities investigation, incidents and accurately assess the impact of the failure so as to make appropriate recommendations on remedial actions for follow-up.
8 days
- We are committed to creating an inclusive workplace and providing equal opportunities for all applicants. We embrace an agile working culture across our roles, so if flexibility is important to you please discuss opportunities with our hiring team. If you need any adjustments to the recruitment process to help you demonstrate your strengths and capabilities, contact [email protected] . Please note this email is for adjustment requests only; for other enquiries please use our standard contact channels.
8 days
- Lead or participate in investigation arising from micro related and utilities investigation, incidents and accurately assess the impact of the failure so as to make appropriate recommendations on remedial actions for follow-up.
8 days
- Ensure that all raw materials / factory samples / intermediates / final products / utilities microbiological monitoring / non-order fulfillment and NCE fulfillment activities are analyzed and tested according to the stipulated quality requirements so as to provide accurate test results for correct usage decisions.
5 days
- GCE ‘O’ or ‘A’ Level in relevant subjects and/or Diploma in Chemical Process Technology or Applied Chemistry
5 days
- Use the appropriate documentation system for the activities being carried out
5 days
- Pro-active with high level of independence
30+ days
- Ensure compliance with site procedures, quality standards and safe work permits.
30+ days
- Ensure project deliverables satisfies GSK Quality Management System (QMS) standards and Engineering Standard (GES) requirements
8 days
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