Biotech Process Development Associate (Lab & GMP)

PERSOL; Singapore; Presencial; SGD 60.000 - 90.000; Jornada completa

Descripción de la vacante

PERSOL is seeking a qualified candidate to support laboratory operations at the Amgen Singapore Manufacturing site. The role involves executing experiments, collaborating with drug substance and process development teams, and documenting findings to enable model qualification and process improvements.

You will assist in data collection, analysis, and the preparation of technical reports, while ensuring GMP-compliant equipment maintenance and readiness.

Formación

• Bachelor’s degree or Diploma required.
• Fields: Chemical engineering, bioprocess engineering, biochemistry, biological sciences.
• Prior internship / relevant experience in a similar capacity.

Responsabilidades

• Support laboratory experiments with Drug Substance and Process Development teams for model qualification and process improvement.
• Plan, execute, and document laboratory studies with data collection, analysis, and interpretation.
• Prepare technical reports, scientific documentation, and study summaries.
• Coordinate laboratory purchasing including PO, invoicing, and receipt of materials while maintaining 5S standards.
• Ensure lab readiness through equipment management and preventive maintenance.
• Support the introduction and qualification of new lab equipment ensuring GMP compliance.
• Contribute to new product introductions and process troubleshooting for biologics manufacturing at ASM site.
• Participate in cross-training and provide support for downstream manufacturing operations as needed.

Conocimientos

Chemical engineering

Bioprocess engineering

Biochemistry

Biological sciences

Internship experience

Educación

Bachelor’s degree

Diploma

Descripción del empleo

PERSOL is seeking a qualified candidate to support laboratory operations at the Amgen Singapore Manufacturing site. The role involves executing experiments, collaborating with drug substance and process development teams, and documenting findings to enable model qualification and process improvements.

You will assist in data collection, analysis, and the preparation of technical reports, while ensuring GMP-compliant equipment maintenance and readiness.