QC Analyst II (Microbiology)

Location: City of Singapore

Company

Global healthcare and biopharmaceutical manufacturing organization developing vaccines, biological products, and other medicines.

What you will do

• Perform microbiological, bioburden, and endotoxin testing of water, raw materials, and product samples.
• Conduct incubation, observation, result recording, and data review.
• Execute environmental monitoring, including viable and non-viable sampling.
• Sample purified water, water for injection, and clean steam, and perform aseptic sample dispensing.
• Write QC documents, including standard operating procedures and risk assessments.
• Maintain complete records in line with GMP data integrity requirements and contribute to continuous improvement.

Requirements

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

Culture & Benefits

• Opportunity to contribute to the start-up of a new, state-of-the-art QC laboratory.
• Work on fully digitalized manufacturing facilities supporting vaccine and biological platforms, including mRNA.
• Environment focused on quality excellence, continuous improvement, and more sustainable manufacturing.
• Equal-opportunity workplace welcoming people from diverse backgrounds.