CMS Manufacturing Process Engineer I

Sanofi; Singapore; On-site; SGD 90,000 - 140,000; Full time

Job summary

Sanofi is seeking an Engineer, Manufacturing to serve as the technical owner for Central Manufacturing Services (CMS). You will drive continuous improvement, change management, and operational reliability across CMS processes and equipment including Media/Buffer prep, Autoclave ops, Column Packing, and Automated Logistics.

You will partner with MSAT, Quality, and Automation to implement robust processes, lead investigations, and ensure GMP-compliant operations with data-driven decision-making.

Qualifications

• Bachelor’s or Diploma in Biotechnology, Biochemical Engineering, Chemical Engineering, Life Sciences, or related discipline.
• 3–5 years of GMP biopharmaceutical manufacturing operations, process engineering, or technical support.
• Experience leading continuous improvement or change-control initiatives with measurable outcomes.
• Experience with process data analysis and deviation investigation is advantageous.

Responsibilities

• Own CMS process and equipment system integrity and performance.
• Lead continuous improvement initiatives with measurable cost/time/yield benefits.
• Develop and manage change controls for process improvements and system upgrades.
• Collaborate with MSAT, Quality, Automation to enhance process control and analytics.
• Drive reliability improvements, preventive maintenance, and risk assessments (FMEA).
• Support qualification, validation, and periodic reviews for CMS systems.

Skills

CMS processes

Change leadership

Data analysis

GMP compliance

Root cause analysis

Lean Six Sigma

Education

Biotech/Biochemical Eng

Life Sciences

Tools

Single-use Systems

Job description

Sanofi is seeking an Engineer, Manufacturing to serve as the technical owner for Central Manufacturing Services (CMS). You will drive continuous improvement, change management, and operational reliability across CMS processes and equipment including Media/Buffer prep, Autoclave ops, Column Packing, and Automated Logistics.

You will partner with MSAT, Quality, and Automation to implement robust processes, lead investigations, and ensure GMP-compliant operations with data-driven decision-making.