QC Microbiology Trainee — CCP Career Path

Sanofi; Singapore; On-site; SGD 32,000 - 42,000; Full time

Job summary

Sanofi in Singapore is seeking a QC Microbiology Trainee under the Career Conversion Programme (CCP). The 15-month local attachment develops skilled biopharma manufacturing professionals through hands-on microbiology testing and GMP-compliant lab work.

You will support routine QC analyses, environmental monitoring, and method transfers while gaining exposure to advanced biopharmaceutical operations and digital lab tools.

Qualifications

• Diploma or degree in Pharmaceutical Sciences or related life sciences.
• Internships or industrial attachments in biopharma are advantageous.
• Self-starter and independent worker able to operate in cross-functional teams.
• Able to work in fast-paced environments with tight timelines.

Responsibilities

• Perform QC microbiological testing (Bioburden, Endotoxin) for water, raw materials, and product samples.
• Perform water sampling of clean utilities and environmental monitoring of clean rooms.
• Perform lab equipment maintenance, cleaning, calibration and troubleshooting as required.
• Support general laboratory activities, including housekeeping and staging reagents and consumables.
• Support method transfer, validation and verification activities to ensure robust analytical performance.
• Drive continuous improvement to enhance laboratory efficiency, safety, and performance metrics.
• Ensure adherence to GMP, regulatory guidelines, and internal quality standards.

Skills

QC microbiology testing

Bioburden testing

Endotoxin testing

Water sampling

Environmental monitoring

Equipment maintenance

GMP compliance

Analytical problem solving

Education

Diploma in Pharmaceutical Sciences

Bachelor in Life Sciences

Job description

Sanofi in Singapore is seeking a QC Microbiology Trainee under the Career Conversion Programme (CCP). The 15-month local attachment develops skilled biopharma manufacturing professionals through hands-on microbiology testing and GMP-compliant lab work.

You will support routine QC analyses, environmental monitoring, and method transfers while gaining exposure to advanced biopharmaceutical operations and digital lab tools.