Microbiology QC Analyst I (GMP Lab)

Biopharma Careers

Singapore

On-site

SGD 36,000 - 48,000

Full time

14 days+
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Job summary

Sanofi is seeking a Quality Control Analyst I (Microbiology) for our new Singapore site to establish and operate a state-of-the-art QC laboratory. The role supports the start-up of a digitalized facility focused on multiple vaccine and biological platforms, aligned with global quality standards.

Ideal candidates hold a Bachelor's degree or Diploma in Microbiology or related field, with 1–2 years in GMP-regulated labs, and proven experience in aseptic techniques, environmental monitoring, and

Qualifications

  • Bachelor's degree or Diploma in Microbiology, Biological Sciences, or related field.
  • 1–2 years of hands-on laboratory experience in a GMP-regulated pharmaceutical/biotech setting.
  • Experience with endotoxin testing and environmental monitoring.

Responsibilities

  • Perform microbiological (including bioburden) and endotoxin testing for water, raw materials and product samples.
  • Incubation, observation, and recording of test results.
  • Environmental monitoring including viable and non-viable sampling.
  • Water sampling including Purified water, WFI and clean steam.
  • Aseptic sample dispensing.
  • Write QC documents (SOPs, risk assessments).
  • Maintain records in accordance with GMP data integrity requirements.
  • Contribute to continuous improvement and quality excellence.

Skills

Aseptic technique
Microbiological testing
Environmental monitoring
Endotoxin testing
GMP data integrity
Electronic documentation

Education

Bachelor's degree / Diploma in Microbiology or related

Job description

Sanofi is seeking a Quality Control Analyst I (Microbiology) for our new Singapore site to establish and operate a state-of-the-art QC laboratory. The role supports the start-up of a digitalized facility focused on multiple vaccine and biological platforms, aligned with global quality standards.

Ideal candidates hold a Bachelor's degree or Diploma in Microbiology or related field, with 1–2 years in GMP-regulated labs, and proven experience in aseptic techniques, environmental monitoring, and

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