QC Analyst - QC Microbiology (CCP)

Job Title : QC Analyst - QC Microbiology (CCP) Location : Singapore / Tuas About the Job The Career Conversion Programme (CCP) (Train-and-Place) for Advanced Biopharmaceuticals Manufacturing Executives/Professionals is a talent development programme aimed at building the next generation of skilled manpower for Singapore’s Biopharmaceuticals manufacturing industry in anticipation of hiring demand. This programme is jointly supported by the Workforce Singapore (WSG) and Workforce Advancement Federation (WAF). The training programme consists of 15 months of local attachment at Sanofi (Aventis-Pharma). Only candidates eligible for CCP programme may apply. Our Company: We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s life. We turn the impossible in to the possible by discovering, developing and delivering medicines and vaccines for millions of people around the world. The Sanofi Modulus is at the cornerstone of our strategy as it aims at creating a new manufacturing concept consisting of a new generation of evolutive multi-product facilities, modular, adaptable and agile, leveraging new disruptive technologies, to better address biologics business challenges. In this context, we are looking for one Quality Control Microbiology Trainee (Career Conversion Program) to support in routine microbiological testing activities. Main Responsibilities: The candidate will have a routine operational role consisting of the following: Perform QC microbiological testing (Bioburden, Endotoxin etc) for water, raw materials, and product samples Perform water sampling of clean utilities system and environmental monitoring of clean rooms Perform laboratory equipment maintenance, cleaning, calibration and troubleshooting as and when required Support general laboratory activities, including laboratory housekeeping and staging of chemicals, reagents, and consumables Support method transfer, validation, and verification activities to ensure robust analytical performance Drive continuous improvement initiatives to enhance laboratory efficiency, safety, compliance, and performance metrics (e.g., deviation/OOS rate, sample turnaround time) Ensure adherence to GMP, regulatory guidelines, and internal quality standards About You Diploma or Degree in Pharmaceutical Sciences, Applied Science or related life Sciences disciplines. Candidate with prior internships or industrial attachments in biopharmaceutical and biotechnology organizations would be advantageous. Self-starter and independent worker who can operate and perform in cross functional teams. Possess strong analytical and critical thinking skills with the ability to problem solving and navigate through complexity and ambiguity. Able to work in fast paced and dynamic conditions with tight timelines. Why choose us? . Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply. Power industry-leading performance by leveraging digital, data, and AI-driven innovation at speed and scale. Transform lives worldwide by delivering life-changing treatments anywhere, anytime. Grow, thrive, and make an impact in a workplace that empowers you to bring your best self every day, with pride. Work with AI, robotics, and next-gen automation to redefine global manufacturing and supply Pursue progress , discover extraordinary Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people. At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com !