Quality Control Specialist

Role overview

Mirxes is hiring a Quality Control Specialist to join its Quality team in Singapore. The role focuses on supporting everyday QC activities, keeping thorough and accurate records, and checking products at multiple points in the manufacturing flow, from incoming raw materials through to intermediates, in-process materials, and finished goods. You will also help investigate nonconforming products and contribute to corrective actions based on inspection findings.

Key responsibilities

• Carry out routine QC tests on incoming raw materials, in-process materials, and final products.
• Organize and plan both scheduled and ad hoc QC runs assigned by the line manager.
• Review results, assess data, and prepare reports that flag any departures from SOP requirements.
• Log nonconformances when issues are identified during QC runs.
• Assist with troubleshooting and root-cause investigations for nonconforming materials or products.
• Prepare new QC work instructions and update existing ones when needed.
• Support validation and stability work for laboratory development activities and diagnostic products as required.
• Provide general lab support such as cleaning and housekeeping, equipment upkeep, document filing and archiving, and tracking laboratory reagent inventory.
• Help improve laboratory procedures and workflows so they remain aligned with GMP expectations.
• Maintain all records using Good Documentation Practices to ensure traceability, transparency, and readiness for audits.
• Take on additional related duties as business needs change, with reasonable accommodations where appropriate.

Required background and competencies

• A diploma or degree in Biomedical Science, Biotechnology, Molecular Biology, Biochemistry, Life Sciences, or a related field is required or equivalent.
• Hands-on exposure to qPCR, including operating qPCR instruments, will be an advantage.
• Comfort using common laboratory equipment such as pipettes and centrifuges.
• Basic familiarity with laboratory processes; experience in assay-based work and QC testing is beneficial.
• Ability to work independently with limited supervision and also collaborate with cross-functional teams.
• Strong planning, organization, and time-management skills.
• High level of initiative and accountability.
• Positive, proactive, and eager-to-learn attitude.
• Good interpersonal and communication skills.
• Basic computer literacy, including Microsoft Office.
• 2 to 3 years of relevant QC experience, preferably in medical device manufacturing.
• Working knowledge of GDP and cGMP is preferred.

Additional information

This position is located in Singapore. Only shortlisted candidates will be contacted.