About the Job Sanofi Manufacturing and Supply organization is preparing its future through an ambitious program named Modulus. The Modulus Project is at the cornerstone of Sanofi 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 vaccine business challenges as well as Specialty Care Biologics products.
Seeking a seasoned and visionary leader with a wealth of hands-on experience in biopharma/API process engineering and automation controls. Possess strong track record in driving project delivery from feasibility study to execution and controls. The ideal candidate thrives in a dynamic environment, bringing strategic thinking, cross-functional leadership, and a passion for developing high-performing teams — all in pursuit of challenging and rewarding work as the Head of Engineering and Projects within the Tuas Modulus Site Engineering & Maintenance team.
Accountabilities
• Manage Tier3 (T3, Experience, Knowledge and Skills
• Only candidates with strong technical acumen, a proven track record in leading equipment/process troubleshooting and commissioning efforts, and the ability to provide hands-on guidance and mentorship to engineers should apply.
• Only candidate with prior GxP experience need to apply
• Degree or Master in Engineering (Chemical / Mechanical / Electrical / Industrial & Systems)
• Minimum 10 years of cumulative experience in Project Management, C&Q and Process Engineering in biopharmaceuticals or API manufacturing. Only candidate with all three areas of expertise will be considered.
• Proven track record in planning, executing, and monitoring large-scale projects
• Hands-on experience with DeltaV automation systems, instrument connectivity, and equipment design is advantageous, with the ability to engage directly at the technical level when required.
• Demonstrated hands-on technical capability, with a proven ability to work alongside engineers on the floor, troubleshoot complex issues directly, and lead by example rather than by setting direction alone
• Excellent analytical and problem-solving skills to address technical issues
• Regulatory Knowledge: Familiar with local statutory requirements, pharmaceutical industry regulations including GMP and FDA standards.
• Commitment to quality and safety; compliance in all project phases
• Strong people management skills and demonstrated ability to work with cross functional teams
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.
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