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Sanofi

Quality Control Analyst I

Sanofi

Singapore • Penuh Waktu

Jadilah yang pertama mendaftar

Pengalaman
1–2 tahun
Gaji
Lowongan
1
Diposting
4 jam yang lalu
Mode kerja
Di kantor
Pendidikan
Bachelor's degree or Diploma in Microbiology, Biological Sciences, or related scientific discipline
Kelayakan
Candidates with a bachelor's degree or diploma in Microbiology, Biological Sciences, or a related scientific discipline, and 1-2 years of laboratory experience in a GMP-regulated pharmaceutical or biotechnology setting, can apply.
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Wajib mendaftar

Tempat Anda akan bekerja

Deskripsi pekerjaan

About the role

Sanofi is expanding its manufacturing network with two new Modulus facilities designed to support more flexible, fully digital production. These sites are intended to increase capacity, improve responsiveness across vaccine and biologics platforms, including mRNA, and reduce environmental impact. In Singapore, the company is looking for a Quality Control Analyst I in Microbiology to help establish and run a modern QC laboratory at the new site, supporting start-up activities while maintaining global quality compliance.

Key responsibilities

  • Carry out microbiology testing, including bioburden and endotoxin analysis, on water, raw materials, and product samples.
  • Manage sample incubation, monitor test progress, and record results accurately.
  • Support environmental monitoring, covering both viable and non-viable sampling.
  • Collect water samples from systems such as Purified Water, WFI, and clean steam.
  • Perform aseptic dispensing of samples in a controlled manner.
  • Prepare and update QC documentation, including SOPs and risk assessment records.
  • Keep all records complete and aligned with GMP data integrity expectations.
  • Contribute to continuous improvement initiatives and a strong quality culture.

Education and experience

A bachelor's degree or diploma in Microbiology, Biological Sciences, or another related scientific field is required. The role is suited to a graduate or professional with 1-2 years of practical laboratory experience in a GMP-regulated pharmaceutical or biotechnology environment.

Technical and behavioral strengths

The position calls for strong aseptic technique, familiarity with microbiological testing and environmental monitoring programs, working knowledge of endotoxin methods, and an understanding of GMP compliance and data integrity. Experience with electronic documentation tools, careful attention to detail, solid teamwork, proactive communication, and the ability to work well in a fast-moving regulated setting are also important.

Additional information

This is a full-time onsite role based in Singapore. It is focused on the start-up and operation of a new QC microbiology laboratory within a modern manufacturing environment.

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