Site Master Planning and Project Engineer

Eli Lilly Eli Lilly · Pharma · Seishin laboratories, Japan

This role is for a Site Master Planning and Project Engineer in the pharmaceutical industry, focusing on strategic site master plans and capital projects to support manufacturing growth, ensuring compliance with global and local regulations. The role involves project management, engineering design, stakeholder collaboration, cost control, and continuous improvement within a regulated manufacturing environment.

What you'd actually do

  1. Develop, maintain, and update the long-range site master plan, incorporating business growth forecasts, technological advancements, operational efficiency improvements and facility fit-and-finish.
  2. Lead and manage capital projects from conception to completion, including scope definition, budget development, schedule management, resource allocation, and risk mitigation.
  3. Oversee and contribute to the engineering design, procurement, construction, and commissioning phases of various projects, ensuring adherence to safety, quality, and environmental standards.
  4. Collaborate effectively with internal stakeholders (e.g., manufacturing, quality, regulatory, HSE, finance) and external partners (e.g., contractors, vendors, consultants) to ensure project success and alignment with company objectives.
  5. Ensure all project activities and site master plans comply with relevant Japanese regulations, Good Manufacturing Practices (GMP), and Eli Lilly global engineering standards.

Skills

Required

  • Bachelor's degree in Engineering (e.g., Chemical, Mechanical, Civil, Industrial) or a related technical field.
  • Minimum of 7-10 years of experience in site master planning, capital project management, and engineering roles within the pharmaceutical, biotechnology, or a highly regulated manufacturing industry.
  • Proven experience in leading complex engineering projects from initiation to close-out.
  • Strong understanding of GMP, HSE regulations, and quality systems.
  • Experience with facility design, utility systems, and process equipment.
  • Excellent leadership, communication, and interpersonal skills.
  • Strong analytical and problem-solving abilities.
  • Demonstrated ability to manage multiple projects simultaneously and prioritize effectively.
  • Fluency in Japanese (written and spoken).
  • Strong English communication skills (written and spoken).

Nice to have

  • Master's degree is a plus.

What the JD emphasized

  • Minimum of 7-10 years of experience in site master planning, capital project management, and engineering roles within the pharmaceutical, biotechnology, or a highly regulated manufacturing industry.
  • Proven experience in leading complex engineering projects from initiation to close-out.
  • Strong understanding of GMP, HSE regulations, and quality systems.
  • Fluency in Japanese (written and spoken) is essential, and strong English communication skills (written and spoken) are required for interaction with global teams.