Quality Control Analyst I (Microbiology)

Location: City of Singapore; onsite laboratory role

Company

Develops healthcare solutions and operates pharmaceutical and biotechnology manufacturing facilities, including vaccine and biological production units.

What you will do

• Perform microbiological, bioburden, and endotoxin testing for water, raw materials, and product samples.
• Conduct incubation and observation activities and accurately record test results.
• Execute environmental monitoring, including viable and non-viable sampling.
• Collect samples from purified water, water for injection, and clean steam systems.
• Perform aseptic sample dispensing and maintain complete GMP-compliant records.
• Write QC documents, including SOPs and risk assessments, and contribute to continuous improvement.

Requirements

• Bachelor’s degree or diploma in microbiology, biological sciences, or a related scientific discipline.
• Graduate or professional with 1–2 years of hands-on laboratory experience in a GMP-regulated pharmaceutical or biotechnology setting.
• Proficiency in aseptic technique and microbiological testing.
• Experience with environmental monitoring programs and endotoxin testing methodologies.
• Understanding of GMP regulations, data integrity principles, and electronic documentation systems.
• Meticulous approach to testing, documentation, and data review, with proactive communication and effective teamwork.

Culture & Benefits

• Opportunity to contribute to the start-up of a new, state-of-the-art QC laboratory.
• Work in a fully digitalized manufacturing environment supporting vaccine and biological platforms, including mRNA.
• Focus on quality excellence, continuous improvement, and compliance with global quality standards.
• Equal-opportunity workplace with an emphasis on diversity and inclusion.