QA Associate - Bioprocess Lab & Process Improvement

PERSOL; Singapore; In loco; SGD 60.000 - 90.000; Tempo pieno

Descrizione del lavoro

Amgen Singapore Manufacturing is seeking a Laboratory Process Development professional to support laboratory experiments in collaboration with Drug Substance and Process Development teams. You will plan, execute, and document studies, collecting data and interpreting results to drive process improvements.

Contribute to technical reports and study summaries, maintain 5S standards during materials handling, and assist with equipment qualification under GMP guidelines.

Competenze

• Proficiency in laboratory techniques and analytical methods.
• Ability to work independently as well as with a team.
• Demonstrates initiative and a drive for continuous improvement.
• Familiar with good documentation practices.

Mansioni

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

Conoscenze

Lab techniques

Team collaboration

Documentation practices

Initiative & continuous improvement

Formazione

Chemical Engineering / Bioprocess / Biochemistry or related discipline

Descrizione del lavoro

Amgen Singapore Manufacturing is seeking a Laboratory Process Development professional to support laboratory experiments in collaboration with Drug Substance and Process Development teams. You will plan, execute, and document studies, collecting data and interpreting results to drive process improvements.

Contribute to technical reports and study summaries, maintain 5S standards during materials handling, and assist with equipment qualification under GMP guidelines.