About The JobSanofi 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. AccountabilitiesManage Tier3 (T3, Pilot early project optioneeringDrive site Capex committees; Manage evaluation and prioritization of site project and process improvement initiatives. Decide on the initiation and manage funding of capital projects.
Provide project feasibility evaluation and technical front-end studies input to support decision making process with site leadership team and central functionProvide input to Site Master Plan and Strategy PlanningManage project execution work packages, inclusive of contract managementOwn deliverables associated with T3 project end-to-end workstream; from design, procurement, construction and C&QAdvise on strategies to ensure all engineering activities comply with industry regulations and standardsAs part of COP, work with global SME to review and upgrade standards, best Practices & Lessons LearnedImplementing process improvements to enhance efficiency, safety, and quality within the engineering and maintenance groupsSelection and management of external contractors and suppliers to ensure they meet the company’s HSE and Quality standards and requirementsStaffing of Site Engineering and Project team based on site needs and strategic workforce planning from design to qualificationManage T1 & T2 (Global Engineering) project integration to site routine, inclusive of technical/project support post qualification and handover to site.
Manage a team of engineers; nurturing talents, driving performance and development planning. About YouDegree or Master’s in Engineering (Chemical / Mechanical / Electrical / Industrial & Systems)Minimum 10 years of experience in Project Management and Execution in biopharmaceuticals or API manufacturingProven track record in planning, executing, and monitoring large-scale projects. In-depth knowledge of engineering & maintenance principles on pharmaceutical manufacturing processes. Regulatory Knowledge: Familiar with local statutory requirements, pharmaceutical industry regulations including GMP and FDA standards. Process Engineering experience for biopharmaceutical or API manufacturing will be a plus. PMP certification preferredExcellent analytical and problem-solving skills to address technical issues.
Commitment to quality and safety; compliance in all project phasesStrong people management skills and demonstrated ability to work with cross functional teamsnullPursue Progress. Discover Extraordinary. Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve.
Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together. At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.
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