CMS Manufacturing Engineer: Process Reliability & Improvement

Sanofi; Singapore; On-site; SGD 85,000 - 130,000; Full time

Job summary

Sanofi in Singapore is seeking an Engineer, Manufacturing to own CMS processes and equipment. You will drive continuous improvement, manage change controls, and ensure GMP compliance across Media/Buffer prep, Autoclave ops, Column Packing, and Automated Logistics.

You will collaborate with MSAT, Quality, and Automation to optimize process performance, data analytics, and system reliability, delivering measurable cost and time savings while maintaining regulatory readiness.

Qualifications

• Degree in biotechnology, biochemical or chemical engineering, or life sciences.
• 3–5 years in GMP biopharma manufacturing operations or CMS support.
• Track record in continuous improvement, change control, or process optimization.
• Experience with data analysis, deviation investigation, or troubleshooting is advantageous.

Responsibilities

• Own technical integrity and performance of CMS processes and equipment.
• Lead continuous improvement initiatives with measurable outcomes.
• Drive change controls for process or system upgrades.
• Collaborate with MSAT, Quality, Automation to enhance control and efficiency.
• Support risk assessments (e.g., FMEA) and validation activities.
• Provide technical SME support for troubleshooting and decision making.
• Ensure GMP-compliant documentation, data integrity, and audit readiness.

Skills

CMS processes knowledge

Continuous improvement

Data analysis & trending

GMP compliance

Deviation investigation

Lean/Six Sigma familiarity

Technical writing & communication

Cross-functional collaboration

Education

Diploma or Bachelor’s in Biotechnology/Biochemical/Chemical Engineering or Life Sciences

Tools

Single-use Systems

Job description

Sanofi in Singapore is seeking an Engineer, Manufacturing to own CMS processes and equipment. You will drive continuous improvement, manage change controls, and ensure GMP compliance across Media/Buffer prep, Autoclave ops, Column Packing, and Automated Logistics.

You will collaborate with MSAT, Quality, and Automation to optimize process performance, data analytics, and system reliability, delivering measurable cost and time savings while maintaining regulatory readiness.