Senior QC Microbiologist - GMP-Driven Micro Testing

WuXi XDC

Singapore

On-site

SGD 50,000 - 73,000

Full time

9 days ago
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Job summary

WuXi XDC in Singapore seeks a qualified professional to perform quality control microbiological testing of raw materials, in-process, and final products under cGMP conditions for QC release and stability studies.

The role supports equipment qualification, calibration, and maintenance of lab instruments, and contributes to aseptic simulations and method transfers. Strong cGMP knowledge and data integrity are essential.

Qualifications

  • Bachelor’s degree or higher in biological sciences or related field with minimum 3 years of experience.
  • GMP laboratory experience preferred.
  • Strong knowledge of cGMP compliance and a quality mindset.

Responsibilities

  • Perform quality control microbiological testing of raw materials, in-process, intermediates, drug substances and finished products under cGMP conditions for QC release or stability studies.
  • Monitor and test the facility and utilities systems.
  • Support equipment qualification, calibration, preventative maintenance and repairs for laboratory instruments.
  • Assist aseptic process simulations and microbiological method transfer/development/validation/verification/suitability.
  • Maintain laboratory documents and ensure ALCOA data integrity.
  • Maintain training records and 5S housekeeping.
  • Escalate investigations, accidents, near misses and policy breaches in a timely manner.
  • Report to and assist the Manager as required.

Skills

Quality control
Microbiology
GMP
Laboratory testing

Education

Bachelor’s degree in Biological Sciences or related field

Job description

WuXi XDC in Singapore seeks a qualified professional to perform quality control microbiological testing of raw materials, in-process, and final products under cGMP conditions for QC release and stability studies.

The role supports equipment qualification, calibration, and maintenance of lab instruments, and contributes to aseptic simulations and method transfers. Strong cGMP knowledge and data integrity are essential.

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