Job Description:
Latest job information from PSC Biotech for the position of QC Specialist. If the QC Specialist vacancy in Singapore matches your qualifications, please submit your latest application or CV directly through the updated Jobkos job portal.
Please note that applying for a job may not always be easy, as new candidates must meet certain qualifications and requirements set by the company. We hope the career opportunity at PSC Biotech for the position of QC Specialist below matches your qualifications.
Boon Lay Way, Singapore | Posted on 01/19/2026
- Industry Pharma/Biotech/Clinical Research
- City Boon Lay Way
- State/Province South East
Job DescriptionPurpose
- Part of the Micro/EM Team responsible for the following:
- Performance oftesting of EM / product stream samples to meet product release timelines and inaccordance with cGMP regulations and Roche/Genentech standards.
- Supportmanufacturing operations by timely completion of testing and disposition.
- Continuousimprovement of processes and technology, in collaboration with ASAT, to drive rightfirst time and efficiencies.
- Qualification andvalidation of test methods.
- Supportinginvestigations of microbial contamination in production processes, classifiedenvironments, and critical utility systems.
- Ensuring testmethods and data are generated in a compliant manner following cGMPs.
KeyResponsibilities- Testing and review of routine and non-routine environmental, raw material, product related samples in accordance to the Standard Operating Procedures (SOP) and Test Methods (TM).
- Perform EM which includes HVAC / BSC / HLFH / VLFH sampling, fingertips monitoring, compressed gases and water / clean steam sampling in accordance to cGMP procedures when required.
- Documentation and review of results in the Laboratory Information Management System (LIMS) and/or documents in accordance with cGMP Procedures.
- Prepare EM reports / trend graph for product lot release and trend data analysis.
- Review routine data and logbooks.
- General lab support including housekeeping, equipment maintenance, document archival, maintaining logbooks and inventory of lab supplies, etc.
- Problem solving of testing related issues as well as troubleshooting of equipment.
- Author and/or update existing SOPs, Forms, OJTs and TMs as needed.
- Initiate discrepancy record, perform discrepancy assessment and identify corrective actions where necessary.
- Train other analysts on methods and/or SOP.
- Responsible for ensuring that all training required to support / perform GMP activities are completed timely.
- Participate in internal / external audits and regulatory inspections.
- Raise work notification, g2g shopping cart forpurchase of consumables / reagent / media for Lab use. Follow up on the plannedreceipt, Delivery orders, invoices when required.
- Understanding of basic microbiologicalprinciples (bioburden, LAL, plating and counting techniques, etc) and executionof intermediate techniques (DET, AET).
- Participate inproject, validation and process improvement works.
- Perform equipment qualification / maintenance,liaise with external / contract lab / vendor.
- Contribute to the continuous improvement oflaboratory procedures and processes to ensure compliance to GMPs.
- Provide forecast for consumables / reagent /media used and facilitate in budgeting and financial planning.
- Perform sample receipt and storage of QCsamples.
- Manage the life-cycle process for retain andreserve/reference samples.
- Manage and prepare the shipment of samples toReceiving labs.
Leadership- Work co-operatively with the Head of Micro/EM and QC Supervisor to create an environment of strong team spirit, timely and effective communications. Strive towards team’s objectives/goals, takes the initiative and proactively turn ideas into action – to make things happen.
- Engage in proactive measures to promote a positive safety culture while ensuring all applicable Safety, Health and Environment requirements are fulfilled in alignment with corporate policy and local legal requirements.
- Embody PT behaviors, lean principles and methods while fostering a continuous improvement mindset throughout the organization by encouraging experimentation and learning.
- A team player and the willingness to cover other colleagues in continued support of the Micro/EM operations.
- Comply with all RSTO’s Safety, Health & Environmental (SHE) requirements, never put oneself and others at safety & health risks, and report any workplace accidents, near misses and hazards as soon as practicable.
- Observe all RSTO’s site security measures at all times, and report any suspicious characters/objects & damaged security mechanisms to Site Security immediately.
Lean Production System- EmbodyPT Lean Production System (LPS), while demonstrating a continuous improvementmindset and behaviors through the use and application of LPS tools forcontinuous improvement initiatives.
Requirements- Degreein Microbiology, Biology, Biochemistry or any LifeSciences discipline or equivalent
- 1-3years of related working experience for degree holders orequivalent holders with combination of education andrelative work experience
- Relatedworking experience in a biotech or pharmaceuticaloperating environment is a plus
- Knowledgeof cGMP relevant to the pharmaceutical industry
- Knowledgeof laboratory safety procedures
- Ableto determine when to escape issue
- Abilityto organize and plan effectively
- Demonstrateexcellent verbal and written communication skills in English
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Job Info:
- Company: PSC Biotech
- Position: QC Specialist
- Work Location: Singapore
- Country: SG
How to Submit an Application:
After reading and understanding the criteria and minimum qualification requirements explained in the job information QC Specialist at the office Singapore above, immediately complete the job application files such as a job application letter, CV, photocopy of diploma, transcript, and other supplements as explained above. Submit via the Next Page link below.
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