QC Microbiology Trainee (CCP) – Biopharma Manufacturing

SANOFI-AVENTIS SINGAPORE PTE. LTD.; Singapore; On-site; SGD 32,000 - 46,000; Full time

Job summary

Sanofi-Aventis Singapore is launching a Career Conversion Programme (CCP) for Advanced Biopharmaceuticals Manufacturing Executives/Professionals, offering 15 months of local attachment at Sanofi. This CCP is meant to develop talent for Singapore’s biopharmaceuticals industry, supported by government initiatives.

We seek a Quality Control Microbiology Trainee to support routine testing activities in a dynamic, cross-functional environment, with a focus on GMP compliance and continuous improvement.

Qualifications

• Diploma or Degree in Pharmaceutical Sciences or related life sciences.
• Internships or industrial attachments in biopharma advantageous.
• Self-starter, independent in cross-functional teams, with problem solving.

Responsibilities

• Perform QC microbiological testing (Bioburden, Endotoxin) for water, raw materials, and product samples.
• Perform water sampling of clean utilities system and environmental monitoring of clean rooms.
• Maintain, clean, calibrate and troubleshoot laboratory equipment.
• Support general laboratory activities and staging of chemicals, reagents, consumables.
• Support method transfer, validation, and verification activities.
• Drive continuous improvement to enhance efficiency, safety, and metrics.
• Ensure adherence to GMP, regulatory guidelines, and internal quality standards.

Skills

Analytical thinking

Independent worker

Team collaboration

Education

Diploma/Degree in Pharmaceutical Sciences

Job description

Sanofi-Aventis Singapore is launching a Career Conversion Programme (CCP) for Advanced Biopharmaceuticals Manufacturing Executives/Professionals, offering 15 months of local attachment at Sanofi. This CCP is meant to develop talent for Singapore’s biopharmaceuticals industry, supported by government initiatives.

We seek a Quality Control Microbiology Trainee to support routine testing activities in a dynamic, cross-functional environment, with a focus on GMP compliance and continuous improvement.