Job Description
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's strategy as it aims to create a new manufacturing concept consisting of evolutive, multi-product facilities that are modular, adaptable, and agile. These facilities will leverage new disruptive technologies to better address vaccine business challenges as well as Specialty Care Biologics products.
Accountabilities:
1. Manage Tier 3 (T3, Pilot early project option) site Capex committees; evaluate and prioritize site projects and process improvement initiatives. Decide on the initiation and manage funding of capital projects.
2. Provide project feasibility evaluations and technical front-end studies to support decision-making with site leadership and central functions.
3. Contribute to Site Master Plan and Strategy Planning.
4. Manage project execution work packages, including contract management.
5. Own deliverables associated with T3 projects from design, procurement, construction, to C&Q.
6. Advise on strategies to ensure engineering activities comply with industry regulations and standards.
7. Work with global SMEs to review and upgrade standards, best practices, and lessons learned as part of COP.
8. Implement process improvements to enhance efficiency, safety, and quality within engineering and maintenance groups.
9. Manage external contractors and suppliers to meet HSE and Quality standards.
10. Staff the Site Engineering and Project team based on site needs and strategic workforce planning.
11. Manage T1 & T2 (Global Engineering) project integration into site routines, including technical support post-qualification and handover.
12. Manage a team of engineers, nurturing talent, driving performance, and development planning.
About You:
* Degree or Master’s in Engineering (Chemical, Mechanical, Electrical, Industrial & Systems).
* Minimum 10 years of experience in Project Management and Execution in biopharmaceuticals or API manufacturing.
* Proven track record in planning, executing, and monitoring large-scale projects.
* In-depth knowledge of engineering & maintenance principles on pharmaceutical manufacturing processes.
* Familiar with local statutory requirements, pharmaceutical industry regulations including GMP and FDA standards.
* Process Engineering experience for biopharmaceutical or API manufacturing is a plus.
* PMP certification.
* Excellent analytical and problem-solving skills for technical issues.
* Commitment to quality and safety; compliance in all project phases.
* Strong people management skills and ability to work with cross-functional teams.
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