Head of Engineering & Projects (Modulus)

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.

Accountabilities

Manage Tier3 (T3,

Pilot early project optioneering

Drive 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 function

Provide input to Site Master Plan and Strategy Planning

Manage project execution work packages, inclusive of contract management

Own deliverables associated with T3 project end-to-end workstream; from design, procurement, construction and C&Q

Advise on strategies to ensure all engineering activities comply with industry regulations and standards

As part of COP, work with global SME to review and upgrade standards, best Practices & Lessons Learned

Implementing process improvements to enhance efficiency, safety, and quality within the engineering and maintenance groups

Selection and management of external contractors and suppliers to ensure they meet the company’s HSE and Quality standards and requirements

Staffing of Site Engineering and Project team based on site needs and strategic workforce planning from design to qualification

Manage 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 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.

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 preferred

Excellent analytical and problem-solving skills to address technical issues.

Commitment to quality and safety; compliance in all project phases

Strong people management skills and demonstrated ability to work with cross functional teams

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