Senior Project & C&Q Engineer - #1101167

Sanofi


Date: 1 day ago
District: Tuas
Salary: $7,500 - $10,000 / month
Contract type: Full time
Work schedule: Full day
Sanofi

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.

As a Senior Project & C&Q Engineer, you will be responsible for:

  • End-to-end capital project delivery for projects up to €5M including initiation, design, execution, C&Q, handover, and close-out.

  • Provide project feasibility evaluation and technical front-end studies input to support decision making process with site leadership team and central function

  • Monthly capital project reporting on all project KPIs for safety, cost, schedule and resources.

  • Adherence to all mandatory Sanofi and local & regulatory compliance standards and policies including construction safety GMRs, Planet Care standards, GMP, and FDA regulations/standards.

  • Lead and support project sourcing and 3rd party contractor & supplier management to support capital project delivery.

  • Manage project execution work packages, inclusive of contract management

  • Support T1 & T2 (Global Engineering) project integration to site routine, inclusive of technical/project support post qualification and handover to site.

About You

  • Degree in Engineering (Chemical / Mechanical / Electrical / Industrial & Systems)

  • Ideally 3 years of experience in Project Management and Execution in biopharmaceuticals or API manufacturing

  • Proven track record in planning, executing, and monitoring projects.

  • 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 stakeholder & people management skills; ability to efficient work and deliver high performance in cross-functional matrix organization

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