Supervisor, Manufacturing

Sanofi

Tuas, Singapore
Gmp compliance
Safety regulations
Continuous improvement initiatives
The role will be responsible for leading the startup and operation of manufacturing areas to produce engineering and PPQ batches with the aim of commercial production

Job Summary

  • The role will be responsible for leading the startup and operation of manufacturing areas to produce engineering and PPQ batches with the aim of commercial production.
  • You will be responsible to provide field leadership to the team of biotechnologists who will be your direct reports.
  • The working hours of this role are 12-hour rotating shifts (day and night) and also include weekends and public holidays.

Matching Summary

The role will be responsible for leading the startup and operation of manufacturing areas to produce engineering and PPQ batches with the aim of commercial production.

Skills & Requirements

Must-have

  • GMP compliance
  • Safety regulations
  • Continuous improvement initiatives
  • Digitalized and automated capabilities
  • Biotechnology/Pharmaceutical experience

Nice-to-have

  • Self-starter and independent worker
  • Operate in cross functional setting
  • Navigate through complexity and ambiguity
  • Work in fast paced and dynamic conditions

Key Requirements

  • Bachelor's Degree or equivalent with at least 8 years of relevant experience
  • At least 2 years of people leadership experience
  • Experience with cGMP documentation
  • Familiarity with Single Use Systems
  • Previous work experience in a digitalized and automated facility

Work Rights

Not specified

Tailored Resume

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