Biotechnologist / Senior Biotechnologist (1-year Contract)

GSK

Tuas, Singapore
Cgmp and safety requirements
Process optimization and efficiency
Documentation and reporting
Support the set-up of end-to-end production operations within the manufacturing facility to achieve productivity targets and objectives

Job Summary

  • Support the set-up of end-to-end production operations within the manufacturing facility to achieve productivity targets and objectives.
  • Adhere to cGMP and safety requirements, meet project milestones, and participate in commissioning and qualification activities.
  • Comply with all relevant IOQ/commissioning protocol/SOP/batch record requirements and participate in deviation investigation processes.

Matching Summary

Support the set-up of end-to-end production operations within the manufacturing facility to achieve productivity targets and objectives.

Skills & Requirements

Must-have

  • cGMP and safety requirements
  • Process optimization and efficiency
  • Documentation and reporting
  • Quality assurance and compliance
  • Site safety procedures

Nice-to-have

  • Proactive personal development
  • Guidance and support to new joiners
  • Continuous improvement projects
  • Agile working culture

Key Requirements

  • Nitec/Higher Nitec/Diploma in relevant field
  • Experience in regulated industry preferred
  • Basic knowledge of cGMP
  • Contract role (1-year)

Work Rights

Not specified

Tailored Resume

Cover Letter