Associate Director - It Systems Program Manager

Eli Lilly Eli Lilly · Pharma · US: Houston TX, United States +1

Associate Director - IT Systems Program Manager at Eli Lilly, focused on overseeing and aligning multiple programs for new API manufacturing sites. The role involves managing large-scale programs, release train engineering, GxP compliance, stakeholder management, risk management, and resource allocation. Requires a strong business understanding, analytical skills, and the ability to communicate complex technical information. Experience in Pharma and GMP Manufacturing is required.

What you'd actually do

  1. Lead and manage large-scale programs, ensuring alignment with organizational goals and objectives.
  2. Oversee the release train process, coordinating with various teams to ensure timely and efficient delivery of products and services.
  3. Determine when to apply Agile and/or Waterfall techniques to manage project timelines, resources, and deliverables effectively.
  4. Ensure all projects adhere to GxP standards, maintaining the highest levels of quality and regulatory compliance.
  5. Engage with stakeholders at all levels, providing clear communication and regular updates on program status.

Skills

Required

  • Program Management
  • Release Train Engineering
  • Agile/Waterfall methodologies
  • GxP Compliance
  • Stakeholder Management
  • Risk Management
  • Resource Allocation
  • Reporting
  • Business understanding
  • Analytical and problem-solving skills
  • Communication of complex technical information
  • Evaluation of new technologies
  • Pharma and GMP Manufacturing experience
  • Bachelor's degree in IT, project management or related field
  • Minimum 10 years of experience in program or portfolio management
  • Experience managing large-scale, cross-functional projects and programs
  • Experience working with project management methodologies (Agile, Waterfall, Scrum, etc)

Nice to have

  • Experience managing programs/projects in the pharmaceutical business
  • Previous experience in the startup of a new facility or clinical development manufacturing site
  • Proven leadership experience in managing cross-functional teams
  • Active participation in industry forums and standards organizations

What the JD emphasized

  • GxP Compliance
  • Pharma and GMP Manufacturing
  • startup of a new facility