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Expect scenarios on GMP deviations, change control, and leading shifts when equipment or data systems fail. Prepare examples of coaching under pressure and how you used digital tools to cut right-first-time issues without bypassing quality.
Strong fit if you have hands-on biotech or sterile manufacturing leadership, comfort with SOP-heavy environments, and interest in digital ops at a global pharma company in Singapore.
As Biotech Manufacturing Supervisor (GMP & Digital Ops) at Sanofi Singapore, a typical day centers on floor and batch readiness under GMP: shift handovers, deviation/CAPA follow-ups, and coaching operators. Digital ops work means checking MES/SCADA or batch-record systems, escalating quality holds, and aligning production, QA, and engineering so throughput stays compliant.
No mapped cert catalog was provided. Prioritize documented GMP supervision, batch release discipline, investigation writing, and fluency with digital manufacturing systems (MES, eBR, shop-floor analytics) used in biotech plants.
No. The listing is Singapore-based with remote set to on-site.
Applying shop-floor systems and data (e.g. MES/eBR) so GMP manufacturing runs with traceable, right-first-time records—not pure IT.
Website: sanofi.us/l/us/en/index.jsp
Sanofi S.A. is a French multinational pharmaceutical and healthcare company headquartered in Paris. The corporation was established in 1973 and merged with Synthélabo in 1999 to form Sanofi-Synthélabo. In 2004, Sanofi-Synthélabo merged with Aventis and renamed to Sanofi-Aventis, which were each the product of several previous mergers. It changed its name back to Sanofi in May 2011. The company trades as "SAN" on Euronext Paris and "SNY" on Nasdaq in the United States, and is a component of the Euro Stoxx 50 stock market index. In 2023, the company was ranked 89th in the Forbes Global 2000.
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Biotech Manufacturing Supervisor - GMP & Digital Ops at Sanofi in Singapore What This Role Involves The role of a Biotech Manufacturing Supervisor at Sanofi involves leading the startup and operation of manufacturing areas for commercial production. You will guide a biotechnologist team, ensuring Good Manufacturing Practices (GMP) compliance and safe operations. The position requires working in 12-hour rotating day/night shifts, including weekends and public holidays, with cross-functional collaboration to optimize process performance. Day-to-Day Responsibilities Lead the startup and operation of manufacturing areas for commercial production. Guide a biotechnologist team in GMP compliance and safe operations. Collaborate across cross-functional teams to optimize processes. Work in 12-hour rotating day/night shifts, including weekends and public holidays. Skills & Qualifications Proven experience as a Biotech Manufacturing Supervisor or similar role. Strong understanding of GMP regulations and compliance practices. Leadership skills to guide a biotechnologist team effectively. Ability to work in rotating shifts, including weekends and public holidays. About Sanofi Sanofi is a global healthcare company committed to transforming lives through the power of human health. Based in Tuas, Singapore, we are seeking a highly skilled Biotech Manufacturing Supervisor to join our team. The role offers an opportunity to contribute significantly to the commercial production process while ensuring safety and compliance. Apply Today To apply, complete your application directly on this page, or you'll be redirected to the employer's application platform to finish submitting there.
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