On-Site Biotech Intern: GMP Manufacturing & Digital Tools

Sanofi; Singapore; On-site; SGD 13,000 - 20,000; Full time

Benefits offered by this job

Company transport to MRT

On-site facilities

Job summary

Sanofi Manufacturing and Supply (M&S) Modulus Singapore is seeking an Intern Biotechnologist, Manufacturing to join the on-site team at the Tuas facility. You will contribute to GMP operations and support commissioning, qualification activities, and tech transfer across Upstream, Downstream and Central Manufacturing Services.

The role emphasizes hands-on experience with digital systems (MES/ERP) and regulatory readiness, in a fast-paced biomanufacturing environment with potential shift

Qualifications

• Self-starter with ability to work independently and with cross-functional teams.
• Strong analytical and critical thinking skills to navigate complex situations.
• Excellent verbal communication and presentation skills; capable of tailoring messages for different audiences.
• Proficient in technical writing and documentation of processes and findings.
• Reliable team player who supports collective success.

Responsibilities

• Perform and support commissioning and qualification activities for equipment and digital systems (e.g., automation, MES, ERP, PCS).
• Execute routine GMP manufacturing operations in compliance with processes, Quality and Safety standards.
• Maintain cleanliness and organization of manufacturing areas per housekeeping procedures.
• Assist in regulatory readiness activities and audit support; contribute to documentation readiness.
• Use digital tools to perform manufacturing tasks and record operations; participate in continuous improvement initiatives.

Skills

Self-starter

Analytical thinking

Effective communicator

Technical writing

Team player

Education

Diploma/Degree in Biotechnology or Life Sciences

Tools

MES

ERP

Job description

Sanofi Manufacturing and Supply (M&S) Modulus Singapore is seeking an Intern Biotechnologist, Manufacturing to join the on-site team at the Tuas facility. You will contribute to GMP operations and support commissioning, qualification activities, and tech transfer across Upstream, Downstream and Central Manufacturing Services.

The role emphasizes hands-on experience with digital systems (MES/ERP) and regulatory readiness, in a fast-paced biomanufacturing environment with potential shift