Biologics Process Engineer: SUS, NPI & Troubleshooting

No-Deviation-Pte.-Ltd

Singapore

On-site

SGD 90,000 - 130,000

Full time

3 days ago
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Job summary

No deviation is a dynamic provider of pharmaceutical services in Singapore, actively supporting biologics manufacturing and NPI activities. We are seeking a Process Engineer with a strong biologics background to optimize Single-Use System–based processes, troubleshoot issues, and drive GMP-compliant improvements.

The role requires collaboration with Manufacturing, MSAT, Quality, Engineering and Validation teams, delivering technical shop-floor support, process changes, and readiness for new

Qualifications

  • Degree in Chemical/Biochemical Engineering, Biotechnology, Life Sciences or related field.
  • 3–6 years of biologics/biopharmaceutical manufacturing experience.
  • Experience with Single-Use Systems, deviations, change controls, troubleshooting.
  • NPI or tech transfer experience is advantageous; solid GMP understanding.

Responsibilities

  • Act as Process Engineer for SUS activities and support biologics manufacturing.
  • Troubleshoot SUS defects, process issues and decontamination activities.
  • Support deviation investigations, root cause analysis and CAPA implementation.
  • Own/support manufacturing process changes, single-use systems and NPI activities.
  • Support NPI and manufacturing readiness, including process documentation and implementation.
  • Provide technical and shop-floor support during manufacturing and NPI.
  • Collaborate with Manufacturing, MSAT, Quality, Engineering and Validation teams.

Skills

Biologics manufacturing
Troubleshooting
Process readiness
CAPA implementation
NPI involvement

Education

Chemical/Biochemical Engineering
Biotechnology
Life Sciences

Tools

Single-Use Systems
Deviations handling
Change controls
GMP knowledge

Job description

No deviation is a dynamic provider of pharmaceutical services in Singapore, actively supporting biologics manufacturing and NPI activities. We are seeking a Process Engineer with a strong biologics background to optimize Single-Use System–based processes, troubleshoot issues, and drive GMP-compliant improvements.

The role requires collaboration with Manufacturing, MSAT, Quality, Engineering and Validation teams, delivering technical shop-floor support, process changes, and readiness for new

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