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Associate Director

2 months ago

Denver, United States Eli Lilly Full time

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.

Key Role Deliverables:

  • Establish and support implementation of lean manufacturing initiatives in alignment with the Lilly Manufacturing Standards of Operational Excellence (MSOEs).
  • Monitor/build a strong safety culture and holding others accountable while leading by example
  • Ensure consistency of operations across shifts through active engagement on the shop floor and through Gemba walks and Practice vs. Procedure evaluations.
  • Participates and/or lead cross functional teams in the development and implementation of strategies associated with the area for the following initiatives: Continuous Improvement, Root Cause Analysis (RCA), Failure Modes Effect Analysis (FMEA), etc.
  • Deliver necessary information and data about the new/ongoing CI projects
  • Facilitates problem-solving, shared learning and decision-making across plant functions
  • Responsible for schedule tracking, updating and reporting to all stakeholders for CI projects.
  • Establishes and implement project management processes and methodologies to ensure CI projects are delivered on time, adhere to high quality standards and meet team expectations.
  • Responsible for assembling Continuous Improvement (CI) project plans, teamwork assignments, directing and monitoring work efforts daily.
  • Escalates technical and timeline issues appropriately for CI projects.
  • Identifies issues that may delay project deliverables and recommends risk mitigation strategies, contingencies, and actions, when appropriate.
  • Serve as CCI Champion partnering with Business Area Leads to facilitate the chosen methodology for the given project (e.g., Lean Lighthouse, Kaizen Event)
  • Other duties as assigned.
Systems & Strategies - Design and Governance:
  • Lead the establishment of the CCI & OE systems (e.g., the Lean Production, Lean Management systems, and our digitally integrated visual management system) within assigned areas, including the components and their interactions.
  • Facilitate the deployment of system standards.
  • Facilitate and execute the process of systems governance and assessment - i.e., health, maturity, and performance - as well as the continuous improvement of the systems.
  • Capture benefits of CCI program and report to site & executive leadership teams
  • Contribute to the CCI&OE program strategy within the assigned area of responsibility (site/function)
  • Collaborate with central CCI&OE function to provide input into the CCI & OE systems design
Instructing and Training Others:
  • Facilitate CI & OE training to all levels of employees within assigned areas to support deployment and ongoing sustainability of CI&OE / Lean ways of working
  • Serve as technical coach for other CCI associates to build their Manufacturing operations and LEAN/ Six Sigma and program management skill set
Minimum Requirements:
  • Bachelor's degree in Engineering, scientific field or related field
  • 5+ years experience in Operations or Manufacturing Support in Pharmaceuticals
Additional Preferences:
  • Certified Lean Six Sigma Black Belt, Master Black Belt or similar level of Lean Coach / Practitioner Certification.
  • Experience with leading projects/improvement initiatives using a CI methodology / tool set including coaching, teaching and mentoring.
  • Demonstrated ability to lead change while managing multiple, shifting priorities.
  • Previous experience in device assembly or packaging operations.
  • Strong problem-solving, critical thinking and analytical skills
  • Strong technical aptitude and ability to train and mentor others
  • Demonstrated ability to maintain a safe work environment
  • Excellent interpersonal, written and oral communication skills
  • Previous experience in operations or directly supporting a pharmaceutical manufacturing operation.
  • Knowledge of lean manufacturing principles and concepts
  • Advanced computer skills are required (Data Analysis - run charts, pareto charts, pivot tables).
  • Strong organizational skills and ability to handle and prioritize multiple requests.
  • Strong technical aptitude and ability to train and mentor others.
  • Qualified candidates must be legally authorized to be employed in the United States.
  • Strong communication skills, both written and verbal, with ability to influence across organizational levels and to facilitate teaching and training of others
  • High level of self-awareness and emotional intelligence
  • Ability to work well in am ambiguous environment with changing priorities.
  • Previous experience with highly automated equipment, Maintenance, engineering
  • Previous equipment qualification and process validation experience.
  • Previous experience with Manufacturing Execution Systems and electronic batch release.
  • Previous experience with deviation and change management systems including Trackwise.
  • Previous experience with Device Assembly or Packaging.
Other Information:
  • The position is 100% onsite for the Lilly Research Triangle Park site.
  • Periodic travel may be required (