Manufacturing Operations Supervisor - 12h Shifts

Sanofi

Singapore

On-site

SGD 90,000 - 130,000

Full time

14 days+
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Job summary

Sanofi is seeking a Supervisor, Manufacturing in Tuas, Singapore to lead startup and operations for engineering and PPQ batches within a modern, digitalized facility. You will oversee a team of biotechnologists, ensure GMP compliance and safety, and drive continuous improvement across manufacturing processes.

The role requires a university degree with substantial experience, plus leadership in a GMP environment and familiarity with DeltaV/MES systems.

Qualifications

  • University degree or equivalent with at least 8 years of relevant experience.
  • Biotechnology/Pharmaceutical background with at least 2 years of people leadership in Manufacturing.
  • Experience with cGMP documentation and record maintenance.
  • Familiarity and prior working experience with DeltaV and MES would be preferred.

Responsibilities

  • Lead the startup and operation of the manufacturing areas to produce engineering and PPQ batches.
  • Provide field leadership to the team of biotechnologists.
  • Ensure GMP, safety regulations and company procedures are followed.
  • Troubleshoot equipment and process issues.
  • Maintain accurate production records and documentation.
  • Initiate and implement continuous improvement initiatives.
  • Collaborate with cross-functional teams to support the manufacturing process lifecycle and deviations, CAPA.

Skills

Team leadership
Analytical thinking
Problem solving
Communication skills

Education

University Degree or equivalent

Tools

DeltaV
MES
Single Use Systems

Job description

Sanofi is seeking a Supervisor, Manufacturing in Tuas, Singapore to lead startup and operations for engineering and PPQ batches within a modern, digitalized facility. You will oversee a team of biotechnologists, ensure GMP compliance and safety, and drive continuous improvement across manufacturing processes.

The role requires a university degree with substantial experience, plus leadership in a GMP environment and familiarity with DeltaV/MES systems.

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