Quality Microbiologist - GMP, Fermentation & EM

SCALEUP BIO PTE. LTD.

Singapore

On-site

SGD 60,000 - 90,000

Full time

4 days ago
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Job summary

ScaleUp Bio in Singapore is seeking a Microbiologist to support microbiological testing, environmental monitoring, contamination control, and laboratory operations in a GMP-regulated CDMO environment. You will ensure microbiological quality and regulatory compliance across materials, processes, utilities, and cleanrooms, while working with cross-functional teams in a fast-paced manufacturing setting.

The role requires hands-on execution, strict documentation, and participation in audits and CAPA

Qualifications

  • Diploma or Bachelor's in Microbiology, Biotechnology, Life Sciences or related field.
  • Minimum 3–5 years of microbiology lab experience.
  • Experience in food manufacturing, fermentation, or biopharma preferred.
  • Strong knowledge of aseptic techniques and microbial testing.

Responsibilities

  • Perform routine microbiological testing of materials, in-process samples, and finished products.
  • Execute environmental monitoring programs for cleanrooms and facilities.
  • Review results for accuracy and compliance; support deviations and CAPA.
  • Operate and maintain laboratory equipment and coordinate calibrations.
  • Support audits, inspections, and change controls to ensure GMP compliance.
  • Assist in method validation and tech transfer activities.

Skills

Microbiology testing
Environmental monitoring
GMP compliance
Audit support
Laboratory operations

Education

Diploma/Bachelor's Degree in Microbiology / Biotechnology / Life Sciences

Tools

HPLC
Spectrophotometers
Autoclaves
Biosafety Cabinets

Job description

ScaleUp Bio in Singapore is seeking a Microbiologist to support microbiological testing, environmental monitoring, contamination control, and laboratory operations in a GMP-regulated CDMO environment. You will ensure microbiological quality and regulatory compliance across materials, processes, utilities, and cleanrooms, while working with cross-functional teams in a fast-paced manufacturing setting.

The role requires hands-on execution, strict documentation, and participation in audits and CAPA

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